Executive Editor, HCP Omnichannel Content
Medical writer job in Atlanta, GA
**Please only local candidates to Atlanta GA
83738
TSR is a premier National U.S. Staffing company with over 50 years of staffing excellence.
Our client, a leading medical publishing company is hiring an Executive Editor, HCP Omnichannel Content for a 6+ months RTH contracting assignment.
Must have skills:
Bachelors degree in Journalism, Communications, Marketing, Design or a related field
Minimum of 3 years of experience in digital content ideation and development
Strong storytelling skills and creative thinking about how to engage audiences
Understanding of how to use AI to help drive optimal creation
Experience with a variety of content types: text, imagery, multimedia, interactive and channel-drive types (e.g., social)
Deep knowledge of health and medical topics, ideally with some familiarity with healthcare professional needs
Preferred skills:
Demonstrated strong content judgement
Advanced editing and storytelling skills
Curiosity about audiences, ideas and information
Ability to interpret and explain statistical data
Pay: $47-48/hour W2
Location: Atlanta GA (hybrid)
Responsibilities:
The editor ideates and creates tests of omnichannel content to support our audience-first strategy, with a primary focus on engaging healthcare professionals (HCPs)
This position also helps maintain successful omnichannel content tests with ongoing content, ensuring performance stays stable or grows
This position partners tightly with our marketing innovation team to ideate and execute our ideas for attracting and engaging audiences across our channels and platforms
The ideal candidate has strong creative abilities, excellent communication and organizational skills, and an understanding of medicine and science
Adept at managing multiple projects and changing priorities and working within a matrixed organization
Technical Writer
Medical writer job in Atlanta, GA
About this Role:
The Revenue Operations Department needs an enthusiastic, diligent, and fast-paced technical writer who can effectively collaborate with stakeholders and subject matter experts to develop clean, concise, easy-to-read documentation. They will be helping Revenue standardize its many operations and enhancing the relationship between Operations, Sales, and our Customers.
What you will do:
Support the maintenance and organization of document repositories, ensuring version control and accessibility.
Conduct independent research and consult with SMEs to understand, question, and refine the information/processes being documented.
Understand and condense complex information/processes into clear and concise documentation.
Coordinating with SMEs on updating or creating SOPs for accounts within their respective portfolio.
Assist in drafting, formatting, and updating documentation under the guidance of a senior technical writer.
Participate in team meetings and collaborative sessions to observe and contribute to discussions with stakeholders and subject matter experts.
Become proficient in the Zavanta platform, to ensure effective management and organization of documentation.
Seek opportunities to suggest improvements to documentation processes, fostering a mindset of continuous improvement.
Build relationships with team members and SMEs, developing communication skills essential for effective technical writing.
What you will need to succeed:
A creative mindset, critical thinking skills, and an eagerness to challenge the status quo. Able to constantly look for process improvement and simplify complex information. You will also need to be able to cultivate relationships with various stakeholders and SMEs and work as part of a fast-paced team.
Curiosity and initiative to independently explore new processes, tools, and business areas.
The ability to break down complicated topics and present them in a digestible way.
Strong relationship-building skills to connect with subject matter experts and team members across departments.
A drive to spot inefficiencies and suggest practical improvements.
Willingness to learn new documentation platforms and adapt to evolving technology.
The confidence to ask questions, challenge assumptions, and seek clarity when information is ambiguous.
A collaborative mindset-valuing feedback, sharing ideas, and contributing to group success.
Typically Preferred:
• Bachelor's Degree preferably in English, Communications, Technical Communication, or Technical Writing. Will consider previous experience in a technical writing environment.
Technical Writer
Medical writer job in Lawrenceville, GA
echnical Writer - 12-Month Project (Onsite)
Duration: 12-month project
We're seeking an experienced Technical Writer to support a large enterprise IT organization on a full-time, onsite basis. This role is ideal for someone who excels at translating complex technical concepts into clear, user-friendly documentation for both technical and non-technical audiences.
You'll partner closely with IT leadership, engineers, developers, and business stakeholders to produce high-quality documentation that supports systems, processes, hardware, software, and user procedures.
Responsibilities
Strategy & Planning
Work with department leaders and end users to define documentation needs for hardware, software, and business processes.
Analyze project requirements to determine required document types.
Gather and interpret technical information from system and development teams.
Content Development & Delivery
Plan, write, edit, and produce a wide range of documents including user guides, manuals, technical specifications, training materials, and policy documentation.
Maintain accuracy and consistency across all documentation.
Edit contributions from various IT team members to create unified and professional deliverables.
Ensure documentation aligns with organizational standards and meets audience needs.
Create visuals (diagrams, charts, graphics) to enhance comprehension.
Preferred Skills
4+ years of technical writing experience
Experience documenting IT systems, software, and processes
Proficiency in Microsoft Word, Excel, PowerPoint, Publisher, and general desktop publishing
Strong attention to detail and excellent written communication skills
Ability to translate complex technical concepts into user-friendly language
Strong interviewing, research, and information-gathering skills
Highly organized, self-directed, and capable of meeting deadlines
Principal Medical Writer- FSP
Medical writer job in Atlanta, GA
**Parexel FSP is looking for a Principal Medical Writer! This is a remote role anywhere in the United States or Canada.** Job Purpose: The Medical Writer, Medical Writing, is responsible for writing and overseeing the completion of a broad range of documents in support of company products and projects. This individual will work with the lead and/or program medical writer and independently to develop messages and write, substantively rewrite, and edit documents for clarity and accuracy, ensuring high quality.
This individual will help manage project documents and timelines, as well as ensuring that documents comply with International Committee on Harmonization guidelines, Sponsor SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member, this individual will work with domestic and international colleagues across R&D (as appropriate).to ensure that documents meet the company's objectives.
Key Accountabilities:
Oversight of activities
- Write and edit clinical regulatory documents for clarity, and accuracy
according to Sponsor standards.
- Work with lead writer and project team to develop document messages
and data presentations within submission timelines to meet company objectives.
- Provide writing support for a wide range of documents, including but not
limited to investigator's brochures, clinical study protocols and reports, integrated summaries, literature reviews, and SOPs.
- Ensure that documents comply with International Conference on
Harmonization guidelines, Sponsor Pharmaceuticals SOPs, and Good Clinical Practices.
Collaborative relationships
- Collaborates effectively with lead writers and project teams to develop
and refine clinical regulatory documents that align with Sponsor standards, ICH guidelines, and Good Clinical Practices, ensuring clear and accurate communication of study data and objectives within submission timelines.
Compliance with Parexel standards
- Complies with required training curriculum
- Completes timesheets accurately as required
- Submits expense reports as required
- Updates CV as required
- Maintains a working knowledge of and complies with Parexel processes,
ICH-GCPs and other applicable requirements
Skills:
- At least 4 years of writing experience in the pharmaceutical industry
- Experience with a variety of regulatory and clinical documents
- Experience in a matrix team environment
- Knowledge of ICH and CTD guidelines for clinical and regulatory submission documents
Knowledge and Experience:
- Ability to write and edit complex material to ensure accuracy and clarity,
- Excellent written and oral communication skills and demonstrated problem-solving abilities
- Ability to handle multiple projects and short timelines
- Ability to work cooperatively with colleagues in a wide range of disciplines
Education:
- BA/BS or higher
\#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Medical Writer
Medical writer job in Kennesaw, GA
Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons' most difficult challenges in treating patients with aortic diseases. Artivion has over 1,400 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com.
Position Overview:
Responsible for creating, editing, and managing high-quality scientific and regulatory documents that support the development, approval, and lifecycle management of medical devices. This role involves working cross-functionally with internal stakeholders-including Clinical, Regulatory, R&D, and Quality teams-to ensure timely and compliant documentation in line with global regulatory requirements. Manage assigned departmental project tasks/systems in principal areas or responsibilities identified below.
Responsibilities:
Writing regulatory documents supporting clinical deliverables for product lines.
Ensure product line compliance with US and International regulations and standards, as applicable to clinical regulatory requirements, including document preparation and submissions.
Coordinating deliverables for the CER, PMCF, and SSCP process for product lines.
Collaborate with Clinical, R&D, Quality, Regulatory, Risk Management, Field Assurance, and Marketing.
Effectively communicate timelines and assist teammates in keeping them.
Conduct literature reviews and write research summaries related to product lines.
Prepare product IFUs and assist with labeling and labeling changes (including receipt of applicable translations).
Collect, query, analyze, distribute and present clinical and pre-clinical data. Develop and maintain any applicable clinical research databases, as necessary.
Interface with technical representatives, regional managers, and research teams for the purpose of technical training and addressing customer questions/concerns.
Generate interim and final clinical study reports.
Communicate with customers and field staff regarding the planning of clinical trials, complaints, problems, and general correspondence.
Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing literature.
Develop clinical protocols and/or investigational plans, informed consent forms, case report forms, handouts, SOPs, analyses, etc. as needed. Prepare status reports, as required.
Perform literature reviews and reference management using tools such as PubMed and EndNote.
Other assigned responsibilities (including previously identified tasks being performed at a higher level than one's current title).
Qualifications:
Education:
Bachelor's degree in life sciences, biomedical engineering, medical writing, or related field (advanced degree preferred: MS, PhD, PharmD, or MD).
Experience:
2-5 years of medical writing experience in the medical device, pharmaceutical, or healthcare industry.
Familiarity with regulatory documentation for medical devices and understanding of applicable regulations (EU MDR, FDA 510(k), etc.).
Skills:
Excellent written and verbal communication skills.
Strong attention to detail and organizational skills.
Ability to interpret complex scientific and clinical data.
Proficiency with Microsoft Office (Word, Excel, PowerPoint) and reference management software.
Preferred Qualifications:
Experience with Class II or III medical devices.
Familiarity with document management systems.
Knowledge of systematic literature review methodology.
Certification or training in medical writing (e.g., AMWA, EMWA) is a plus.
Medical Writer, CME Grants
Medical writer job in Atlanta, GA
Medscape, a division of WebMD, develops and hosts physician portals and related mobile applications that make it easier for physicians and healthcare professionals to access clinical reference sources, stay abreast of the latest clinical information, learn about new treatment options,
earn continuing medical education credits and communicate with peers.
WebMD is an Equal Opportunity/Affirmative Action employer and does not discriminate on
the basis of race, ancestry, color, religion, sex, gender, age, marital status, sexual orientation,
gender identity, national origin, medical condition, disability, veterans status, or any other
basis protected by law.
POSITION SUMMARY:
Medscape Education is seeking an experienced grant writer to play a primary role in the
development of proposals seeking funds to develop continuing medical education
(CME) programs, which are published on the leading healthcare professional education
site, Medscape.org. This is a hybrid position out of our Atlanta or Newark offices.
Responsibilities:
Working primarily in HEMATOLOGY/ONCOLOGY, the writer is responsible for all steps
and interactions required to write and prepare proposals for submission within agreed
focus, budget, and time scale to the highest quality and with minimal supervision.
Specific tasks include, but are not limited to:
Ensure proposals are clinically appropriate and instructionally sound and adhere to
ACCME standards
Lead proposal initiation calls with internal stakeholders to obtain details and direction
for proposal development, confirming and clarifying timelines, clinical focus and
grant focus, educational tactics, outcomes assessment plans, and other details as
required
Write clear, succinct needs assessments that provide evidence for identified clinical
practice gaps and/or patient education gaps, which follow recognized standards and
are supported by internal and external data
Use internal templates and tools to develop proposals that tell a compelling story on
the rationale, instructional design, and value of the proposed educational solution
Incorporate revisions based on input from cross-functional internal and external
proposal reviewers, including account managers, clinical strategists, medical
education directors, and copyeditors, to ensure high-quality grant submissions and
improve likelihood of external grant awards
Qualifications:
Bachelor's degree in life sciences, public health, clinical sciences, journalism,
technical writing, or English may also be considered or equivalent years of
experience; advanced degree in a medical or science-related specialty is a
differentiator
2 years' experience in writing and editing within the medical education field,
including work at a medical education/communications company, professional
medical publisher, academic institution/hospital/university center, or medical society;
previous grant writing for a medical education or scientific organization is a
differentiator.
Excellent editorial (editing and writing) skills, preferably in the area of grant/proposal
and needs assessment development
A flexible mindset and excellent time management and organizational skills to
manage multiple projects and tasks simultaneously in a highly deadline-driven
environment, while taking into consideration stakeholders based across multiple
time zones
Ability to deliver results with minimum supervision by suggesting plausible solutions
and creatively using existing resources in a productive and/or innovative way to
quickly deal with unforeseen issues and to ensure that timelines are consistently met
Strong ability to "think outside of the box" and customize grant proposals for
maximum storytelling impact and clarity
Superior communication and interpersonal skills (verbal, written, listening)
Excellent computer skills, which include working remotely on shared networks and
cloud-based systems
Attention to detail with high level of accuracy
Positive attitude, high energy, and willingness to accept varied assignments
Available and responsive to communications during business hours
Availability for a limited amount of domestic and international travel (~10%), mainly
to onsite team meetings
Ability to maintain friendly and productive relationships with internal and external
stakeholders through clear articulation and an effective communication style
Process oriented, able to find new ways to improve existing processes and to learn
and adapt to evolving processes and tools
Preferred Skills:
At least 2 years' experience working with cross-functional teams and external
partners toward common objectives
Superior ability to describe medical/public health issues, clinical scenarios, and
complex scientific data to a non-technical audience
Superior ability to incorporate data, visuals, and narrative into a compelling written
story
High degree of proficiency using Microsoft Word; at least basic skill level in Excel,
PowerPoint, and Adobe Acrobat
Experience using Salesforce, SharePoint Online, Workfront, Tableau, Google Suite,
Microsoft Teams
Familiarity with and usage of generative AI tools/LLMs for writing efficiency
Salary range: $85,000 - $95,000 Depending on Experience.
Benefits:
Employees in this position are eligible to participate in the company sponsored benefit
programs, including the following within the first 12 months of employment:
Health Insurance (medical, dental, and vision coverage)
Paid Time Off (including vacation, sick leave, and flexible holiday days)
401(k) Retirement Plan with employer matching
Life and Disability Insurance
Employee Assistance Program (EAP)
Commuter and/or Transit Benefits (if applicable)
Eligibility for specific benefits may vary based on job classification, schedule (e.g., full-time vs.
part-time), work location and length of employment.
Auto-ApplyProposal Writer
Medical writer job in Atlanta, GA
Sharecare is the leading digital health company that helps people - no matter where they are in their health journey - unify and manage all their health in one place. Our comprehensive and data-driven virtual health platform is designed to help people, providers, employers, health plans, government organizations, and communities optimize individual and population-wide well-being by driving positive behavior change. Driven by our philosophy that we are all together better, at Sharecare, we are committed to supporting each individual through the lens of their personal health and making high-quality care more accessible and affordable for everyone. To learn more, visit ******************
Job Summary:
The Proposal Writer is responsible for developing a range of proposal content that meets proposal compliance and quality standards. The incumbent develops proposal content in coordination with the Proposal Manager and the proposal team.
Essential Job Functions:
Research, write, and edit persuasive and compliant proposal content that aligns with Sharecare's brand voice, value propositions, and solution differentiation
Partner cross-functionally with internal stakeholder groups (i.e., Sales, Product, Security, Legal, and Operations) to validate accuracy.
Ensure timely submission, formatting consistency, and adherence to brand and quality standards.
Translate complex health, wellness and technology concepts into clear, audience-specific messaging that demonstrates value and impact.
Leverage proposal management software (e.g., Loopio) to source, customize, and maintain reusable content that reflects current offerings and standards
Analyze RFP/RFI requirements and contribute to win strategy development.
Support the continuous improvement of the content library by identifying gaps, refreshing outdated material, and integrating feedback from past submissions.
Contribute to post-submission reviews and incorporate lessons learned to improve win rate and proposal quality.
Accept ownership for new and different responsibilities as business priorities shift, exploring and building opportunities to add value
Specific Skills/ Attributes:
Well organized, able to prioritize and re-prioritize work in a dynamic environment to meet changing business needs
Excellent written, oral, and verbal communication skills
Solid problem-solving skills
Lifelong learner, proactively seeks additional opportunities to expand knowledge
Results driven with disciplined follow-through and a focus on accuracy
Strong work ethic, excellent team player, and a "do what it takes" attitude
Demonstrated enthusiasm for intensive, deadline-driven, and high-profile role
Active listening and assessment skills with the ability to take complex technical information and translate information into compelling content
Ability to conceive the client need and write from their perspective
Qualifications:
A Bachelor's Degree in business, communications, English or related field, or equivalent experience. Experience in the healthcare industry is preferred.
Prior RFP/proposal writing experience 2 yrs. Plus 2-5 years' experience in a professional corporate or related environment.
Sharecare and its subsidiaries are Equal Opportunity Employers and E-Verify users. Qualified applicants will receive consideration for employment without regard to race, color, sex, national origin, sexual orientation, gender identity, religion, age, equal pay, disability, genetic information, protected veteran status, or other status protected under applicable law.
Auto-ApplyTechnical Proposal Writer
Medical writer job in Kennesaw, GA
As a Technical Writer, you will collaborate with Pursuit Specialists, Business Development, and technical teams to develop high-quality proposals. Your responsibilities will include drafting, editing, assembling, and submitting both competitive-bid and sole-source proposals. Additionally, you will support the preparation and review of other technical and commercial documents. Working closely with the Pursuit Specialist and division leadership, you will contribute to creating a proposal plan that ensures timely delivery and adherence to the highest quality standards, effectively meeting customer requirements and needs.
This position can be based in one of the following locations:
Kennesaw, GA (Suburb of Atlanta)
Tampa, FL
Overland Park, KS
Naperville, IL (Suburb of Chicago)
Additional office locations may be considered for the right candidate
Responsibilities
Imagine a day where you transform complex RFPs into clear, compelling proposals. You collaborate with cross-functional teams to gather insights, craft persuasive narratives, and ensure compliance. Your attention to detail and organizational skills drive the proposal process from start to finish, delivering high-quality submissions that support business growth.
RFP Analysis & Compliance: Analyze Request for Proposal (RFP) requirements and work closely with the Pursuit Specialist and proposal team to ensure proposal content is complete, relevant, compelling, persuasive and compliant
Proposal Development & Standards: Develop proposals using ENERCON templates and/or customer-provided templates. Follow proposal-writing standards and best practices including readability, consistency and tone
Visual & Technical Communication: Utilize images, tabular data, graphical data, flowcharts, diagrams, and other graphics effectively to support a winning proposal. Ensure complex technical solutions and strategies provided by the proposal team are easily understandable, readable, consistent, and compelling
Proofreading & Unified Voice: Proofread and edit documents for style, consistency, grammar, and syntax. Synthesize text and ideas from multiple authors to ensure one voice throughout proposal
Supporting Documentation: Create and/or edit supporting documents required for proposals including compliance matrices, capability statements, past performance references, personnel bios and resumes, and other documents required by the customer
Template & Database Management: Support maintenance of proposal database and proposal templates
#LI-MB1
Qualifications
Bachelor's Degree in English, Communication, Journalism, or Business
A minimum of 6+ years technical writing experience
Experience writing proposals or handling RFPs (preferred)
Demonstrated writing and editing skills appropriate for competitive-bid proposals
Excellent writing skills including understanding of grammatical rules, punctuation, sentence structure, and active/passive voice
Proficient in Microsoft Word and Adobe
Meticulous attention to detail
Excellent written and communication skills with strong ability to flex/adjust styles to audience
Able to handle confidential information with discretion
Ability to manage multiple priorities and deadlines in a fast-paced, demanding work environment
Strong teamwork skills in a service-oriented environment
Strong organizational skills
Pay Range USD $73,000.00 - USD $128,000.00 /Yr. Additional Information
About ENERCON:
At Enercon Services, Inc. (ENERCON), we're driven by our people-and we're proud to offer rewarding careers in a culture of excellence. We provide a comprehensive benefits package and professional development opportunities that support your long-term growth.
What We Offer:
Enjoy full benefits for you and your dependents starting day one, no waiting period
Flexible work arrangements, including hybrid and alternative schedules
401(k) with employer matching
Tuition reimbursement
Professional Engineer (PE) license support and incentives
Want to see the full picture? Click HERE to see our Comprehensive Benefits
Salary Range Information:
If a salary range is listed, it reflects the typical range for this full-time position based on the role, level, and location. Individual compensation within the range will be determined by factors such as work location, relevant experience, job-related skills, and education or training.
Eligibility to Work:
Candidates must be legally eligible to work in the US without requiring current or future sponsorship.
Ability to pass a pre-employment and random drug and alcohol screenings, ENERCON and client specific background checks, and annual motor vehicle record (MVR) according to company and client policies.
Equal Opportunity Employer:
ENERCON does not discriminate in employment opportunities or practices based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law.
Connect with Us: *************** | LinkedIn
Auto-ApplySr Technical Writer
Medical writer job in Atlanta, GA
Akkodis is seeking a Sr Technical Writer for a Contract job with a client in Atlanta, GA. You will collaborate with global teams to develop high-quality technical content and maintain documentation using modern tools and writing techniques. Rate Range: $43/hour to $45/hour; The rate may be negotiable based on experience, education, geographic location, and other factors.
Sr Technical Writer job responsibilities include:
* Develop and maintain comprehensive technical documentation that aligns with organizational standards and supports both physical and digital products.
* Collaborate with cross-functional global teams including engineering, regulatory, marketing, and product management to gather and review content.
* Apply modern technical writing tools and techniques (e.g., Madcap Flare, Adobe FrameMaker) to ensure clarity, accuracy, and usability.
* Manage multiple documentation projects simultaneously, prioritizing tasks to meet deadlines and ensure timely delivery.
* Continuously update and improve existing documentation artifacts to reflect product changes and user feedback.
Desired Qualifications:
* Bachelor's degree (preferably in Technical Communication or a technical field).
* 5-7 years in a technical documentation role, with at least 2 years working with global teams.
* Superior written and verbal communication skills with high fluency in English.
* Experience using modern documentation tools such as Madcap Flare, Adobe FrameMaker, or other XML-based platforms.
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at *****************************
This position requires the use of information or access to facilities subject to the International Traffic in Arms Regulations (ITAR) and/or Export Administration Regulations (EAR). These regulations may limit access to controlled technologies: 1) to U.S. Persons, including U.S. Citizens, lawful permanent residents, and other narrow categories including some refugees and asylees, or 2) to certain foreign nationals that have received an export license.
Pay Details: $43.00 to $45.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to *************************************************
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
* The California Fair Chance Act
* Los Angeles City Fair Chance Ordinance
* Los Angeles County Fair Chance Ordinance for Employers
* San Francisco Fair Chance Ordinance
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Easy ApplySenior Technical Writer
Medical writer job in Atlanta, GA
Job DescriptionSenior Technical WriterEmployment Type: Full-Time, ExperiencedDepartment: Technology Support CGS is seeking an experienced Senior Technical Writer to provide consultative, analytical, and documentation support for a large Federal agency initiative.
CGS brings motivated, highly skilled, and creative people together to solve the government's most dynamic problems with cutting-edge technology. To carry out our mission, we are seeking candidates who are excited to contribute to government innovation, appreciate collaboration, and can anticipate the needs of others. Here at CGS, we offer an environment in which our employees feel supported, and we encourage professional growth through various learning opportunities.
Skills and attributes for success:- Drafting and development of technical documentation related to a variety of projects in the IT space.- Work closely with project stakeholders to establish technical processes and procedures.- Document projects through the SDLC.- Provide status reports for multiple ongoing projects and related documentation efforts.- Assist with both user and admin level documentation.
Qualifications:- Excellent writing and Communication skills.- 5+ years experience with development of technical documentation.- 3+ years experience with development of user documentation.- Fluency with industry standard technical summary and reporting techniques including Agile project management methodology.- Ability to produce quality work independently or in a group setting.- Experience with MS Office Suite including Visio.- Willingness and ability to pass background check/security screening.
Ideally, you will also have:- Familiarity with Business Intelligence/Analysis applications.- Experience with Government software development policies and procedures.- Client facing communication experience.- Federal Agency issued security clearance.
Our Commitment:Contact Government Services (CGS) strives to simplify and enhance government bureaucracy through the optimization of human, technical, and financial resources. We combine cutting-edge technology with world-class personnel to deliver customized solutions that fit our client's specific needs. We are committed to solving the most challenging and dynamic problems.
For the past seven years, we've been growing our government-contracting portfolio, and along the way, we've created valuable partnerships by demonstrating a commitment to honesty, professionalism, and quality work.
Here at CGS we value honesty through hard work and self-awareness, professionalism in all we do, and to deliver the best quality to our consumers mending those relations for years to come.
We care about our employees. Therefore, we offer a comprehensive benefits package.- Health, Dental, and Vision- Life Insurance- 401k- Flexible Spending Account (Health, Dependent Care, and Commuter)- Paid Time Off and Observance of State/Federal Holidays
Contact Government Services, LLC is an Equal Opportunity Employer. Applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Join our team and become part of government innovation!
Explore additional job opportunities with CGS on our Job Board:**************************************** more information about CGS please visit: ************************** or contact: Email: *******************
#CJ
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Easy ApplySenior R&D Technical Writer - Transfusion and Transplant
Medical writer job in Norcross, GA
We are seeking a Sr. R & D Technical Writer who will be responsible for preparing technical documentation to support IVD design history files and regulatory submissions. Strong understanding of Quality Management Systems and Global IVD Regulations (including but not limited to IVDR and 21CFR820).driven and results-oriented Validation Engineer I to be responsible for assuring the successful execution of Werfen's Validation Program. If you are interested in joining an organization where your talents and expertise will be highly appreciated, and if you meet our qualifications to excel in this position, we want to hear from you. Contact us today!
This position is
not eligible for sponsorship for work authorization
. Therefore, if you will require sponsorship from us for work authorization now or in the future,
we cannot consider your application at this time
.
Responsibilities
Additional responsibilities for Sr. R & D Technical Writer:
Responsible for preparing all required R&D documentation for IVDR products to be in compliance with EU MDR 2017/746 regulation and/or FDA.
Review current or new product documentation to develop strategies to align with cross-functional teams to fulfill the regulatory requirement.
Collaborate with the Regulatory Affairs, Quality Control, Clinical Operations and Project Management organizations to determine requirements and draft/edit documentation for IVD products.
Draft and develop plans, protocols and reports that explain and support the performance of a product to be in compliance.
Understand basic system functionality and operation of instrumentation and reagents to populate plans and reports for the document of the product performance.
Identify and escalate potential document generation improvements to the respective organizations.
Support in proceeding the Audit (onsite or remote) activities by a competent Authority, as required by the team.
Ensure, consistency, completeness, accuracy, and conformance to style guidelines.
Responsible for executing a gap analysis of commercialized IVD products, reviewing reports, and providing guidance to Project Team for updating technical documentation.
Support responses to FDA and EU Notified Body during the preparation and review of submissions.
Strong attention to detail with organizational and technical writing skills.
Mentor and assist in giving on-the-job training and instructions to junior staff
Additional Responsibilities:
Demonstrates strong verbal and written communication skills.
Displays ability to communicate clearly, write technical documentation clearly, legibly fill out documentation to communicate data and details as needed.
Interacts cooperatively with co-workers and receives direction well from managers.
Displays ability to be an effective team member.
Demonstrates knowledge of products, services, procedures, policies, systems and company organization as it relates to job requirements.
Displays PC skills with Microsoft Office (Word and Excel) and other software applications (TrackWise, MasterControl, SharePoint) functions at an intermediate level.
Ability to prioritize multiple workloads.
Interacts effectively with other departments.
Maintain records and files of work and revisions according to procedures and processes by following cGDP.
Qualifications
Other qualifications for this role include:
BS/BA in a related discipline, or advanced degree, where required, or equivalent combination of education and experience.
3+ years of experience within a Regulated Industry (medical device / pharma preferred.)
Experience working on multidisciplinary teams in a fast-paced, dynamic environment.
3+ years of technical writing experience.
Auto-ApplyGrant Specialist: post-award
Medical writer job in Atlanta, GA
The grant specialist is responsible for administering the post-award process at Morehouse College, ensuring that agency-required reports are submitted in a timely manner, and coordinating the closeout of federal grants to the college.. Additional duties include facilitating the issuance and monitoring of sub-awards, providing grant administration training for faculty and staff, assisting with internal and external audits of grants and other sponsored programs, and ensuring the integrity of internal grants controls. The individual who occupies this role will represent Morehouse in grant-related matters with outside funding sources, administer database management activities concerning Morehouse grants and contracts activity, assist with the preparation of reports, and collaborate with other Morehouse College offices to manage and administer federal grants.
Physical Demands
This is an in-person position and the grant specialist will be expected to report to the office during normal business hours. Additionally, the successful candidate must be able to walk across the campus, sit and stand for extended periods of time, and posses a level of dexterity of hands and fingers needed to operate a computer keyboard. They must also be able to read small font on printed on digital media, and lift up to 50 lb. Occasionally, the grant specialist may need to work outside of business hours to meet critical deadlines.
Required Qualifications
Bachelor's degree 2+ years of related experience Knowledge of and experience in obtaining grants/contracts from federal/state/private agencies Knowledge of Uniform Guidance Working knowledge of MS Office Suite, Adobe Acrobat, Google Forms Excellent oral and written communication skills
Preferred Qualifications
Experience working in a college or non-profit setting Research Administrator Certification - CRA
Proposal Writer (Government Contracting)
Medical writer job in Peachtree City, GA
Full-time, Part-time, Contract Description
Company: Certified Technical Experts, Inc. (CTE) Department: Business Development / Proposals
Certified Technical Experts, Inc. (CTE) is seeking a detail-oriented and experienced Proposal Writer to support the development of high-quality, compliant, and compelling proposals for federal, state, and local government opportunities. The Proposal Writer will play a critical role in coordinating inputs from subject matter experts, ensuring compliance with solicitation requirements, and producing clear, persuasive content that positions CTE for successful contract awards.
This position requires strong writing skills, knowledge of the government procurement process, and the ability to work under tight deadlines in a fast-paced environment.
Key ResponsibilitiesProposal Development
Review and analyze RFPs, RFIs, RFQs, and other solicitations to extract requirements and ensure compliance.
Write, edit, and format proposal sections including technical, management, staffing, and past performance narratives.
Collaborate with business development, contracts, IT, and subject matter experts to gather necessary input and tailor content to agency priorities.
Compliance and Quality Assurance
Develop and maintain compliance matrices to ensure all solicitation requirements are addressed.
Edit and proofread proposals for clarity, consistency, and accuracy.
Ensure proposals align with CTE branding, messaging, and win themes.
Coordination and Collaboration
Work closely with Proposal Manager, Capture Managers, and leadership to translate strategies into compelling written responses.
Participate in proposal reviews (Pink/Red Teams) and incorporate feedback.
Support the development of graphics, charts, and other visuals to enhance proposal readability.
Documentation and Templates
Maintain a library of boilerplate content, resumes, and past performance references.
Contribute to continuous improvement of proposal templates, style guides, and processes.
Support knowledge management efforts by capturing reusable proposal content.
Requirements Qualifications and Experience
Experience: Minimum of 3-5 years writing proposals for government contracting (federal, state, or local).
Knowledge: Familiarity with federal procurement processes, FAR/DFARS, and small business programs.
Skills:
Exceptional writing, editing, and proofreading skills.
Ability to translate technical inputs into clear, customer-focused narratives.
Strong organizational skills and ability to meet strict deadlines.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and Adobe Acrobat; experience with proposal management tools is a plus.
Education: Bachelor's degree in English, Communications, Technical Writing, Business, or related field.
About CTE
Certified Technical Experts, Inc. (CTE) is a SBA-certified Small Disadvantaged Business (SDB) and minority-owned firm with nearly two decades of experience supporting federal, state, and local government agencies. We specialize in cybersecurity, IT services, systems engineering, cloud solutions, business services, and staffing. With certifications including ISO 9001:2015, ISO 27001:2013, and CMMI SVC Level 3, CTE delivers innovative, compliant, and mission-focused solutions that empower government clients to achieve success.
Senior Editor - Research Methods (Maternity cover contract to start late January 2026)
Medical writer job in Milton, GA
We currently have an exciting vacancy for an Editor III on the Research Methods list at Routledge. This is a maternity cover contract which will start late January/early February 2026. The role involves the proactive global commissioning of a wide range of books in Research Methods, managing the frontlist programme of new manuscripts for production and directing strategy for this expanding subject area.
The role is varied and motivating, involving working across a wide range of text types from bestselling textbooks and handbooks to professional titles and research level books, with an international range of authors. This is an excellent opportunity for a candidate who would like the chance to implement their own strategic vision and work with enthusiastic and motivated authors, whilst contributing to a fast-growing interdisciplinary list. The role will have overall responsibility for steering the Research Methods list, building upon its strong growth and commercial successes in recent years.
The successful applicant should possess strong commercial awareness, excellent networking skills and the ability to work with internal departments such as production, marketing, rights, and sales to lead the Research Methods list and help ensure revenue goals are met.
What you'll be doing:
* Meeting annual commissioning and revenue goals for the Research Methods list
* Identifying market needs and recruiting authors to write books that meet these needs
* Evaluating book proposals and soliciting peer review
* Proposing suitable projects to the publishing committee, including compiling internal proposal documents and negotiating contract terms with authors
* Working closely with authors, and editorial, production, marketing, and sales colleagues to ensure that goals are met.
* Acting as a product champion with internal stakeholders to ensure buy-in and support for the list across other departments
* Being an ambassador for Routledge and Taylor & Francis and promoting the business to external stakeholders including academic authors, editors, etc.
* Contributing ideas towards global publishing strategies
Executive Editor - HCP Omnichannel Content
Medical writer job in Atlanta, GA
Details:
Stefanini Group is hiring!
Exciting opportunity awaits, let us help you get started!
Click Apply now or you may call: **************/ email: Deepak Tyagi (**************************) for faster processing!
The editor ideates and creates tests of omnichannel content to support our audience-first strategy, with a primary focus on engaging healthcare professionals (HCPs). This position also helps maintain successful omnichannel content tests with ongoing content, ensuring performance stays stable or grows. This position partners tightly with our marketing innovation team to ideate and execute our ideas for attracting and engaging audiences across our channels and platforms.
The ideal candidate has strong creative abilities, excellent communication and organizational skills, and an understanding of medicine and science. This position understands how to drive to business goals. The Executive Director will also be adept at managing multiple projects and changing priorities and working within a matrixed organization.
This role is based in Atlanta and reports to the Executive Director, Omnichannel Content
Responsibilities:
Helps develop and execute the strategy for editorial innovation and evolution across our platforms and channels
Develops or identifies existing test content working with creators
Works with marketing innovation to test concepts
Works with Executive Director and other omnichannel content editors to identify additional content innovation opportunities
Helps develop plans to operationalize successful ideas
Ensure that winning concepts fit tightly with business goals and other product and content supporting them -- ensure that the content universe works together without siloed pieces.
Manage people and teams across a matrixed organization
Details:
Qualifications:
Bachelors degree in Journalism, Communications, Marketing, Design or a related field.
Minimum of 3 years of experience in digital content ideation and development.
Strong storytelling skills and creative thinking about how to engage audiences
Understanding of how to use AI to help drive optimal creation.
Experience with a variety of content types: text, imagery, multimedia, interactive and channel-drive types (e.g., social)
Excellent organizational skills.
Deep knowledge of health and medical topics, ideally with some familiarity with healthcare professional needs
Preferred Skills:
Demonstrated strong content judgement
Advanced editing and storytelling skills
Curiosity about audiences, ideas and information
Ability to interpret and explain statistical data
Commitment to integrity and upholding the highest content standards
Ability to work collaboratively and effectively with colleagues
Ability to evangelize change and innovation
Strong interpersonal skills and a team player mentality
AI prompt creation
*Listed salary ranges may vary based on experience, qualifications, and local market. Also, some positions may include bonuses or other incentives*
About Stefanini Group
The Stefanini Group is a global provider of offshore, onshore and near shore outsourcing, IT digital consulting, systems integration, application and strategic staffing services to Fortune 1000 enterprises around the world. Our presence is in countries like Americas, Europe, Africa and Asia, and more than 400 clients across a broad spectrum of markets, including financial services, manufacturing, telecommunications, chemical services, technology, public sector, and utilities. Stefanini is a CMM level 5, IT consulting, company with global presence. We are CMM Level 5 company.
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Easy ApplyGrant Writer
Medical writer job in Alpharetta, GA
Job Title: Grant Writer
Position Overview: We are seeking a proactive and strategic Grant Writer/Government relations associate to lead our efforts in securing government funding and fostering relationships with governmental agencies. This role is pivotal in aligning our business objectives with public sector opportunities, ensuring compliance, and advocating for policies that support our growth and mission.
Key Responsibilities:
Government Funding Acquisition: Identify, pursue, and secure government grants, contracts, and funding opportunities that align with the company's strategic goals.
Policy Advocacy: Monitor and analyze legislative and regulatory developments; advocate for policies favorable to the company's interests.
Stakeholder Engagement: Establish and maintain relationships with key governmental officials, agencies, and industry associations.
Compliance Oversight: Ensure all company operations and proposals comply with applicable federal, state, and local regulations.
Strategic Planning: Develop and implement comprehensive government relations strategies to advance the company's objectives.
Prepare and submit grant applications, ensuring compliance with federal requirements and deadlines.
Manage post-award grant activities, including budget oversight, reporting, and compliance monitoring.
Develop and maintain systems for tracking grant expenditures, deliverables, and performance metrics.
Ensure all grant activities comply with federal regulations (e.g., 2 CFR Part 200, Uniform Guidance) and organizational policies.
Communication: Prepare and deliver reports, presentations, and briefings to senior management on government relations activities and outcomes.
Requirements
Qualifications:
Bachelor's degree or higher
Minimum of 5 years of experience in government relations, public affairs, or a similar role within a for-profit or non-profit organization
Proven track record of securing government funding and influencing public policy.
Strong understanding of governmental processes and regulatory environments at federal, state, and local levels.
Excellent communication, negotiation, and interpersonal skills.
Life Sciences experience is highly preferred but not required.
We are an equal-opportunity employer and celebrate diversity, recognizing that diversity of thought and background builds stronger teams. We approach diversity and inclusion seriously and thoughtfully. We do not discriminate on the basis of race, religion, color, ancestry, national origin, caste, sex, sexual orientation, gender, gender identity or expression, age, disability, medical condition, pregnancy, genetic makeup, marital status, or military service.
Benefits
PTO
401K
Paid Holiday
Auto-ApplyGrants Specialist
Medical writer job in Roswell, GA
City of Roswell, Georgia
***********************
To perform this job successfully, an individual must be able to perform the essential job functions satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the primary job functions herein described. Since every duty associated with this position may not be described herein, employees may be required to perform duties not specifically spelled out in the , but which may be reasonably considered to be incidental in the performing of their duties just as though they were actually written out in this .
Grants Coordinator
Department: Public Sector
FLSA Status: Exempt
JOB SUMMARY
This position is responsible for managing and coordinating the grant application process, researching and identifying available funding opportunities, developing grant proposals, and working closely with a private grant writing firm. The coordinator collaborates with different departments within the organization to ensure proposals align with the organization's goals and objectives. The coordinator will work the CFO and the Office of the Mayor to ensure strategic alignment between grant solicitation and city strategic priorities.
As a Grants Coordinator, you will be responsible for maintaining accurate grant records, monitoring and reporting the grant status, and ensuring compliance with federal and state guidelines. federal and state and guidelines. You will work with program managers to develop budgets and track grant expenditures. Your communication skills will be essential for maintaining relationships with funding agencies and stakeholders.
A successful Grants Coordinator should possess strong organizational, time-management, and problem-solving skills. Attention to detail, an analytical mindset, and the ability to work collaboratively are also essential for this position.
ESSENTIAL JOB FUNCTIONS
Research and identify potential grants for the organization
Develop and write grant proposals that align with the organization's mission and goals
Work with team members to gather necessary information, data, and budgets for grant proposals
Work in partnership with outside federal grant writers to leverage funding opportunities and lobby federal grants as necessary
Work in partnership with state-based private grant writing firm, including lobbying activities as necessary
Submit grant applications in a timely manner and track progress of applications
Communicate with grant providers and follow up on grant proposals
Develop and maintain relationships with grant providers and other funding organizations
Work with the executive finance team to manage grant budgets and ensure compliance with grant requirements
Maintain accurate records of grants and assist with grant reporting requirements
Responsible for working with departments and finance team on grant audits
Keep up-to-date with changing grant guidelines and regulations
Work with Senior Leadership to organize an annual grant priority strategy session
Assist with other fundraising efforts and events as needed
MINIMUM QUALIFICATIONS
Education and Experience:
A bachelor's degree in a related field like finance, public administration, or business is required. Additional certifications or training in grant management, project management, or budgeting can also be helpful. On the experience side, you should have at least 2-4 years of experience in grants management, budget management, or project management. Experience with Community Development Block Grant process is a significant plus. Experience with government agencies or non-profit organizations is a plus.
Licenses or Certifications:
None
Special Requirements:
None
Knowledge, Skills and Abilities:
Research and identification of grants
Proposal writing and grant application process knowledge
Ability to track, monitor, and report on grants
Knowledge of compliance with federal and state guidelines
Strong organizational and problem-solving skills
Strong communication skills for maintaining relationships with funding agencies and stakeholders
Ability to collaborate across departments and with external firms
PHYSICAL DEMANDS
The work is sedentary to light which requires the ability to exert light physical effort, but which may involve some lifting, carrying, pushing and/or pulling of objects and materials of light weight (5-10 pounds). Tasks may involve extended periods of time at a keyboard or work station. Tasks also require the ability to perceive and discriminate colors or shades of colors, depth, texture, and visual cues or signals. Some tasks require the ability to communicate orally.
WORK ENVIRONMENT
Work is regularly performed without exposure to adverse environmental conditions.
The City has the right to revise this job description at any time. This description does not represent in any way a contract of employment.
The City of Roswell, Georgia commits to a policy of equal employment opportunity for applicants and employees, complying with local, state and federal laws. The City's policy is to employ qualified persons without discrimination regarding race, creed, color, religion, age, sex, country of national origin, marital status, disability, sexual orientation, gender identity, genetic information, political affiliation, ethnicity, or status in any other group protected by federal/state/local law.
Auto-ApplyEditor-in-Chief
Medical writer job in Atlanta, GA
Fueled by the same entrepreneurial spirit that drives those we cover, Hypepotamus generates awareness about the Southeast's innovation community. Hypepotamus.com is the go-to source of startup and technology news, interviews, events, job listings, and resources. We showcase the founders, students, innovators, companies, and investors that are proud to call the Southeast home.
Job Description
Hypepotamus, the leading startup and technology publication in the Southeast U.S. is looking for a new editorial lead. This is a full-time position based in Atlanta.
This is a high-touch role with almost unlimited potential and autonomy. The Editor-in-Chief has full editorial oversight across articles, photography, email newsletters, and social media.
The EIC will manage a small staff of full and part-time employees that work largely remotely. The EIC will hold editorial meetings with the Managing Editor and other staff members, assign articles and interviews, and assess pitches and story ideas. The EIC typically also writes several stories a week.
The EIC serves as the face of the publication in the community, attending events, supporting and connecting community leaders, and speaking on panels and at events when appropriate.
Experience desired:
Editorial: Experience in an editorial or communications role, ideally in written media, is required. Additional familiarity with working on a news cycle, media and public relations, and long-form features are highly desired. A degree in journalism, communications, PR or media would be exceptionally helpful.
Startup/technology familiarity: You will cover companies across a broad range, from recently-founded to acquisition or IPO. Experience working at a high-growth startup, founding your own company (successful or not), or working in or with venture capital or growth equity investors is highly desired.
Management: The EIC manages a small team of dedicated employees along with a network of contributors and freelancers. Organizational and time management skills are essential. People management experience is a big plus.
Community engagement: The EIC attends and occasionally speaks at events that range from casual startup pitch competitions to formal investor conferences. A willingness to attend events (sometimes in early mornings and nights) is required, as well as an ability to comport oneself appropriately. The EIC also participates in local ecosystem-building organizations as part of the role.
This individual will have significant autonomy, and can make his or her own hours and schedule. The publication has several options for co-working space, but there is no one central office. The team stays in touch with regular in-person meetings and email and Slack communication.
Salary is commensurate with experience and healthcare and 401(k) plan with company match are available.
Qualifications
Education and work experience
: 3-5 years of prior work experience and a Bachelor's degree (or equivalent) is required. Those with non-traditional backgrounds or experience are encouraged to apply.
Additional Information
All your information will be kept confidential according to EEO guidelines.
Junior Writer
Medical writer job in Morrow, GA
Collision Estimator Classic Collision is now hiring a Collision Estimator. Classic Collision was established in 1983 in Atlanta, Georgia with one single goal: To offer quality service to its customers with integrity and honesty. Be a part of a rapidly growing company whose mission is to put safety, quality, integrity, and heart into every vehicle we repair and customer we serve.
Classic Collision offers competitive pay, benefits, and career advancement opportunities. The salary range for this position is commission based and dependent on expected sales volume.
Please come and join our team!
Why Choose Classic Collision?
* Paid Weekly
* Continuous Training
* Supportive Team Culture
* Company match 401K
* Medical/Dental/Vision
* Paid Time Off - 6 Paid Holidays
* Rewarding Work
Responsibilities
* Serves as the primary point of contact for the customer throughout the repair process from the point of drop-off through the delivery of the completed vehicle.
* Prepares estimate for customer and or insurance partners according to manufacturer and Classic Collision guidelines.
* Partners with the insurance companies to manage customers claim to insure the best customer experience.
* Maintains communication with customers providing updates on repair process.
* Coordinates with technicians to confirm all aspects of the damages are identified.
* Maintains customer satisfaction scores according to company standards.
* Perform quality inspection prior to vehicle delivery to the customer.
* Perform other related duties as assigned.
Qualifications
* Must be at least 18 years of age.
* Valid Driver's License Required
* Ability to provide clear, concise information in writing, via phone and in-person.
* Prior collision estimating experience preferred.
* Familiar with estimating systems CCC1 preferred.
* I-CAR / ASE certification preferred.
* Strong organizational skills
* Successful completion of background check required.
Behaviors/Competencies
Integrity -Respect, and accountability at every level and in every interaction
Customer Service-Provide the highest level of customer service while building customer satisfaction and retention.
Innovation -Develops and displays innovative approaches and ideas to our business.
Teamwork -Contributes to building a positive team spirit. Supports everyone's efforts to succeed.
Physical & Environmental
While performing the duties of this job, the employee is regularly required to use their hands and is required to talk and hear. The employee is frequently required to stand, sit, and walk occasionally for long periods at a time. The employee may occasionally be required to reach with hands, and arms and move objects up to 20 pounds. Specific vision abilities required by this job include close vision, peripheral vision, and the ability to adjust focus. In addition, abilities for assessing the accuracy, neatness, and thoroughness of the work assigned are required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
Classic Collision is an Equal Opportunity Employer
As an equal opportunity employer, Classic Collision does not discriminate against any employee or candidate based on age, race, gender identity, gender expression, genetic information, national origin, physical or mental disability, protected veteran status, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by all applicable federal, state, and local laws.
Reasonable Accommodations
Classic Collision is an equal opportunity employer that is committed to working with and providing reasonable accommodations to individuals with disabilities. If you have a disability and you believe you need reasonable accommodation to search for a job opening or submit an online application, please e-mail recruiting@classiccollision or ************. This email and phone number are listed exclusively to assist disabled job seekers whose disability prevents them from being able to apply online.
This job description is not a complete statement of all duties and responsibilities comprising the position.
Commercial Proposal Writer
Medical writer job in Cartersville, GA
Job Title Commercial Proposal Writer The Proposal Writer position is responsible for completing a variety of proposals and projects by offering compelling and well-positioned information. The position supports all commercial sales teams at all levels as well as brand marketing teams and the commercial Strategic Sales Support team. The proposal writer is also responsible for providing graphic design support for marketing materials.
Responsibilities:
+ Collaborate with sales and internal teams to understand proposal needs and strategy.
+ Lead meetings to gather information required for proposal responses.
+ Research and understand company operations to write accurate and informed content.
+ Write and format proposals that align with brand standards and present a professional image.
+ Create and manage pricing tables, including international currency conversions.
+ Deliver completed proposals on time, coordinating writing, design, reviews, and approvals.
+ Build and maintain a network of internal experts to support proposal development.
+ Use templates and brand guidelines to ensure consistency and quality in all proposals.
+ Continuously improve proposal content and processes based on feedback and results.
+ Support team goals by taking on new tasks and identifying ways to add value.
+ Coach team members and subject matter experts on effective writing practices.
Qualifications:
+ 4-year degree in communication s , English, j ournalism or 4 years of proposal writing / grant writing experience required
+ Advanced writing and editing abilities both technical and persuasive writing required
+ The ability to work varied hours and have a flexible schedule (up to 4 days a week onsite) required
+ Proficient in Microsoft Word, Excel, PowerPoint and Adobe Creative Suite required
Preferred Qualifications:
+ Eye for design and the ability to work with designers and make simple edits to existing layouts.
+ Excellent problem solver with attention to detail and ability to think strategically.
+ Ability to work in a team environment.
+ Ability to handle multiple competing deadlines
+ Must be able to translate complex technical information into clear communication for a variety of audiences.
Competencies:
+ Deliver Compelling Communication
+ Build Customer Satisfaction
+ Delegate Authority
+ Build Trusting Relationships
+ Execute Action Plan
Shaw benefits include:
+ Medical, dental, and vision insurance
+ Life insurance and disability coverage
+ Tuition reimbursement
+ Employee assistance program
+ Health savings account
+ Paid Time Off
+ Parental Leave
+ 401K and Retirement Plans
+ Product discounts for employees
+ Adoption assistance
+ Shaw Family Health Center (Dalton, GA, and Cartersville, GA, locations)
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Work Shift
8 Hr non-rotating shift, Hrs fall to in punch day, Observed Calendar, shift starts AM
Shaw Industries is an equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities.