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4.6

Medical Science Liaison - Oncology - PA, OH, IN, IL Territory

@Orchard
Medical Science Liaison Job, Remote or Philadelphia, PA
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Medical Science Liaison (MSL)
Oncology Work from Home
Territory: Pennsylvania, Ohio, Indiana & Illinois (Lower Great Lakes) Are you an MSL with proven KOL relationships within academic and other hospital ecosystems focused upon Oncology?
Do you have relationships with stakeholders within leading institutions within the hospital ecosystem centered upon Oncology?
Are you excited by the prospect of supporting life-saving products serving both solid tumor and hematology-related cancers?
Are you someone able to work independently, with minimal direction, and still deliver great results?
Do you want to work for a US-based pharmaceutical firm, owned by a global powerhouse, with an exceptional new product pipeline within the Oncology field, and significant career opportunities for top performers?
If the answer is “yes” to these questions, we would like to hear from you.
@Orchard LLC has been retained by a growing pharmaceutical firm focused solely upon Oncology to lead a search for an experienced Medical Science Liaison (MSL) able to work from a home office, with travel, and support a multi-State territory (the current need is to support the Lower Great Lakes regions of IL, OH, PA & IN). Your focus will be to engage Key Opinion Leaders within the most influential teaching and academic centers and other oncology-focused institutions within the territory to understand unmet needs and introduce them to our client’s products and research.

About our client;
Looking for a chance to make a real difference in the oncology space? Our client is on a mission: to improve the lives of cancer patients, their families, and caregivers. Their “People first” approach means they also value their employees, who work relentlessly to help us execute the client’s mission. Our client’s success is founded on ensuring they always act with accountability, collaboration, and trust. By following these guiding principles, they earn and maintain the confidence of patients, partners, and each other. Our client is focused on a goal to discover and develop innovative cancer treatments that address unmet patient needs and apply the science behind them in novel ways. As the field of cancer treatment evolves, they evolve with it.

Advanced technology, dedicated investigators, and incomparable facilities: these vast resources empower us to redefine the way the world treats cancer.

It’s our client’s work, passion, and legacy. If the prospect of being part of this sounds exciting, we invite you to connect with us to learn more.

About the role;

As an MSL supporting a defined territory, you will;
  • Facilitate and develop the relationship with the medical/scientific community within your assigned territory, by communicating scientific products and disease state elated information to investigators and institutions.
  • Provide information on research developments and new concepts in medical treatment, giving perspective to field activities associated with the medical science benefits of existing products and new products.
  • You will build lasting and qualitative relationships with key opinion leaders (KOLs) within Oncology in your territory.
  • You will be tasked with bringing back requests for information and insights from your KOLs to the company.
Your responsibilities will include;
  • Identify, establish, and maintain collaborative relationships with key investigators and institutions strategic to the appropriate use of company products.
  • Participate in medical education for healthcare professionals, through presentations at appropriate venues.
  • Facilitate the identification of medical community training and educational needs, and work with the appropriate departments to ensure required education and training are provided.
  • Increase visibility for our client with current and future industry leaders.
  • Identify clinical research opportunities that are consistent with company objectives.
  • Be the key contact for investigators for the initiation of ISS, and provide investigators with technical support for study development.
  • Identify and communicate key clinical and research issues from industry leaders to appropriate departments to help shape company research, development, marketing plans, and strategies.
  • Maintain clinical expertise through aggressive education including attendance at relevant conferences, scientific workshops, and review of key journals.
Your background will likely include;

Educational Requirements:
PharmD., Ph.D. or MD (with clinical experience within the US preferred), or a Masters in Nursing, or related field and clinical experience as a Nurse or Nurse Practitioner within the Oncology space.

Professional Experience:
  • This is a field-based position working from a home office: must be available for frequent travel.
  • 5 years overall experience as an MSL preferred, with a minimum of 2 years Oncology.
  • Demonstrable clinical trial development experience.
  • Knowledge of treatment guidelines, clinical research processes, FDA regulations, and OIG guidelines.
  • Excellent interpersonal verbal and written communication and presentation skills are required.
  • Proven ability to network and partner with important external customers, including medical thought leaders, academic institutions, large group practices, medical directors, and pharmacy directors is required.
  • Our client is experiencing significant growth and therefore a high level of positive self-motivation and adaptability to rapidly changing demands is essential for your long-term success.
If your experience and interests align with this role, and you want to align your career with a stable and growing firm with an excellent pipeline of products within Oncology, then we need to hear from you. Please apply.
Established in 2010, @Orchard has an exceptional reputation, providing staffing solutions to time-sensitive, talent scarcity issues to deliver better talent management ROI. Our specialty lies in the critical area of program talent acquisition and resource management, not in one narrow skillset, but across many areas of technical and functional delivery. To learn more about our other exciting opportunities, visit our Jobs Page at www.atorchard.com .
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Mid Level
33d ago
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3.8

Medical Science Liaison, Reimbursement (Open to Remote, Hybrid or On-Site)

Guardant Health
Medical Science Liaison Job, Remote or Palo Alto, CA
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We re committed to building for the future, focusing on optimizing billing and reimbursement and ensuring we stay true to our company mission and values in the process.As a Medical Science Liaison, Reimbursement, you play an important role in the overall success of the company.
Mid Level
9d ago
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4.8

Psychiatrist - Consultant Liaison, Virtual | Reliant Medical Group

Optum
Medical Science Liaison Job, Remote or Worcester, MA
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As a part of the Optum network, Reliant Medical Group is seeking a Psychiatrist to join our growing team in Massachusetts with multiple practice locations available. At Optum, we are transforming healthcare nationally while providing Physician-led care locally. As part of Optum, we've found that putting clinicians at the center of care is the best way to improve lives. Optum is a drug-free workplace. 2019 Optum Health & Technology.
Mid Level
Professional
Doctorate Preferred
New
1d ago
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3.8

Medical Science Liaison, Reimbursement (Open to Remote, Hybrid or On-Site)

Guardant Health
Medical Science Liaison Job, Remote or Palo Alto, CA
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As a Medical Science Liaison, Reimbursement, you play an important role in the overall success of the company.
Mid Level
8d ago
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Sr. Clinical Scientist - Remote

Penfield Search Partners
Senior Clinical Scientist Job, Remote or Fairfield, CT
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Our client is seeking a Senior Clinical Scientist to lead a clinical study and assist senior clinical development staff in the preparation and review of clinical documents, clinical research and develop and deliver presentations.
Mid Level
Senior Level
Masters Preferred
15d ago
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Clinical Scientist (Remote Opportunity)

Katalyst Healthcares & Life Sciences
Clinical Scientist Job, Remote or Franklin Lakes, NJ
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Responsibilities:
  • Participate as the Clinical Representative in Post-Market Clinical Surveillance Prepare Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) for technical documentation in compliance with applicable regulations (e.g., MEDDEV 2.7.1, ISO 14155, EU MDR, etc.) and company procedures.
  • Collaborate with other writers to ensure continuous improvements in writing style, harmonization of terminology, and team initiatives. Responsible for ensuring that assigned plans and reports are self-checked for errors, grammar, accuracy before approval, and that documents are routed correctly in the document control process. Responsible for following up on approvals of documents and ensuring that the CERs are released in the electronic document system timely.
  • Obtain required approvals and ensure that Clinical Evaluations remain current according to the required update schedule. Participate in work streams and or process improvement initiatives.


Requirements:
  • Bachelor's degree in a relevant field or clinical/medical subject area (e.g., Biology, RN, PA, etc.) with 5 years of professional experience.
  • Master's Degree, Medical Doctor, Nurse, Pharmacist, Doctor of Philosophy in a relevant field or clinical/medical subject area with 5 years of professional experience is strongly preferred.
  • Scientific research, medical writing, or medical device industry or a combination of education and experience preferred.
  • This position requires demonstrated experience in high quality medical/technical writing and excellent written and oral communication skills.
  • Prior experience performing clinical evaluations according to MEDDEV 2.7.1 and EU MDR, and systematic literature reviews is strongly preferred.
Mid Level
Bachelors Required
9d ago
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4.4

Clinical Scientist

Beacon Hill Life Sciences-Boston
Clinical Scientist Job, Remote or South San Francisco, CA
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Our Client is seeking a highly motivated Clinical Scientist to be responsible for bringing together clinical, scientific, and technical disciplines to ensure high-quality protocol development, study execution, and data interpretation. Our Clinical Scientist is a key member of our clinical team and partners closely with other clinical team members, applying technical and scientific excellence to support the development and execution of clinical trials to meet the needs of internal and external customers. Our Clinical Scientist responsibilities impact key elements of the study lifecycle including protocol development, safety monitoring, data quality review, patient narratives, and preparation of Clinical Study Reports.
Mid Level
Masters Required
21d ago
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3.8

Clinical Scientist (Remote Opportunity)

Katalyst Healthcares Life Sciences
Clinical Scientist Job, Remote or Franklin Lakes, NJ
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Responsibilities:
  • Participate as the Clinical Representative in Post-Market Clinical Surveillance Prepare Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) for technical documentation in compliance with applicable regulations (e.g., MEDDEV 2.7.1, ISO 14155, EU MDR, etc.) and company procedures.
  • Collaborate with other writers to ensure continuous improvements in writing style, harmonization of terminology, and team initiatives. Responsible for ensuring that assigned plans and reports are self-checked for errors, grammar, accuracy before approval, and that documents are routed correctly in the document control process. Responsible for following up on approvals of documents and ensuring that the CERs are released in the electronic document system timely.
  • Obtain required approvals and ensure that Clinical Evaluations remain current according to the required update schedule. Participate in work streams and or process improvement initiatives.
Requirements:
  • Bachelor's degree in a relevant field or clinical/medical subject area (e.g., Biology, RN, PA, etc.) with 5 years of professional experience.
  • Master's Degree, Medical Doctor, Nurse, Pharmacist, Doctor of Philosophy in a relevant field or clinical/medical subject area with 5 years of professional experience is strongly preferred.
  • Scientific research, medical writing, or medical device industry or a combination of education and experience preferred.
  • This position requires demonstrated experience in high quality medical/technical writing and excellent written and oral communication skills.
  • Prior experience performing clinical evaluations according to MEDDEV 2.7.1 and EU MDR, and systematic literature reviews is strongly preferred.
Mid Level
Bachelors Required
New
6d ago
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4.5

Clinical and Health - Scientist I, Formulation

Integrated Resources, Inc.
Clinical Scientist Job in Frederick, MD
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Job Description: Company Information

About ***

*** Inc. (NYSE: TMO) is the world leader in serving science, with revenues of *** billion and 50,000 employees in 50 countries. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and increase laboratory productivity.We offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive support.

Job Description
Job Title: Scientist 1 Manufacturing (Formulations)

Position Summary:

Work in a Value Stream environment and formulate molecular biology reagents for use in research and commercial scientific products for the life sciences industry. The formulations range in scale from 1 Client to 1,000 L and are manufactured using protocols/batch records in an environmentally monitored lab space. Data is recorded in batch records following good documentation practices as required for regulated industries.

This is a Third Shift position and requires the successful candidate to work Monday through Friday, 10pm - 6:30 AM. Some weekend work may be required as determined by plant management.

New hire training may be scheduled for either First Shift (6:00 AM - 2:30 PM) or Third Shift.

Key Objectives of the role:

Executes on the formulation of reagents and solutions in a fast-paced manufacturing environment following controlled documents and procedures.

Utilize specialized technical knowledge and skills to make detailed observations and analyze data within operating parameters.Actively participate in troubleshooting for specific processes or activities as assigned.

Maintain equipment, product inventory, and related records as assigned.Note variances on manufacturing documents; audit and evaluate process documents and propose revisions.

Identify manufacturing procedures intended to optimize existing processes and ensure compliance with regulatory requirements.

Advise the team lead/supervisor of factors that may affect quality of the product, initiate problem reports for deviations and non-conforming materials and suggest options and ideas for corrective actions and preventive actions (CAPA).

Minimum Qualifications:

Bachelors degree in Biology, Molecular Biology, Biochemistry, Biotechnology, or other related discipline and 2+ years of experience in a manufacturing or research laboratory OR 6+ years of experience in a biotech/pharmaceutical GMP environment.

Proficiency in the use of scientific laboratory techniques, equipment and materials including:
- Aseptic techniques
- Scales and balances
- pH/Conductivity meters
- Mixers and stir plates
- Pipetting
- Spectrophotometer operation (Nanodrop)
- Large scale solution formulation in fixed and mobile tanks
- Fume hood/Biological Safety Cabinet (BSC)
- Snorkel dust collectors
- Good documentation practices (GDP)

Safety awareness and identification of potential safety issues.

Bench work in an ISO Class 8 clean lab environment with specialized equipment.
Ability to carry out scientific procedures and make recommendations for improvement.

Excellent documentation and communication skills.

Lifting up to 40 lbs will be required.

Must be flexible to work varying schedules and hours as needed including weekends.

Must be able to work safely with chemicals and hazardous materials.

The noise level in the work environment is usually moderate.

May be required to stand for long periods of time while performing duties.

May intermittently sit at desk/lab bench for a long period of time to perform experiments, write, and use a keyboard to communicate through written means.

Preferred Qualifications:

Ability to work independently and/or in a group setting.

Works on assignments that are complex in nature where judgment is required in resolving problems and making routine recommendations.

Experience in ISO 90001, ISO 13485 and/or GMP manufacturing environment.

Displays positive attitude toward job and others.

Good problem-solving skills.

Good knowledge of current Good Manufacturing Practices (cGMP) and experience with cGMP documentation and Microsoft applications is preferred.
Comments for Suppliers: This position is ment to be a Temp to Perm hire
Mid Level
Bachelors Required
New
7d ago
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4.0

Clinical and Health - Scientist I, Formulation

Talentburst, Inc.
Clinical Scientist Job in Frederick, MD
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Location: Frederick, MD
Senior Level
Bachelors Required
New
7d ago
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Director/Senior, Clinical Pharmacology (Remote Eligible)

Adlai Nortye USA Inc.
Director, Clinical Pharmacology Job, Remote or North Brunswick, NJ
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Adlai Nortye is seeking a Director/Senior director for insuring clinical pharmacology support for a portfolio of oncology projects.
Senior Level
Executive
Masters Required
New
7d ago
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4.9

Principal Medical Writer- GI - Remote

Takeda Pharmaceutical
Medical Writer Job, Remote or Boston, MA
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Principal Medical Writer, GI - Remote Join us as a Principal Medical Writer in our Cambridge or Lexington office. As a Principal Medical Writer working on the Medical Writing team, you will be empowered to formulate the writing strategy for key clinical and regulatory documents and regulatory submissions; guide medical writing document preparation coordination of assignments to Takeda and contract writers; provides review and substantive editing of documents. Working across therapeutic areas with a focus on Gastroenterology to provide expert support as needed the Principal Medical Writer formulates the writing strategy for key clinical and regulatory documents and regulatory submissions; guides medical writing document preparation, including coordination of assignments to Takeda and contract writers; provides review and substantive editing of documents. Reporting to a Medical Writing Team Lead, the Principal Medical Writer guides medical writing activities for key clinical and regulatory documents and regulatory submissions.
Senior Level
New
6d ago
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4.8

Associate/Director, Clinical Pharmacology Modeling & Simulation (CPMS) - Remote

Parexel
Director, Clinical Pharmacology Job, Remote or Alaska
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Director, Clinical Pharmacology Modeling and Simulation (CPMS)
Executive
Masters Preferred
New
7d ago
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Medical Writer (CER Writer)-Remote

Clinchoice Inc.
Medical Writer Job, Remote or Fort Washington, PA
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of roles and responsibilities: The Medical Writer will provide technical and strategic writing activities and expertise for regulatory and evidence summary documents throughout the product development and life cycle process.
Mid Level
Doctorate Preferred
Bachelors Required
New
2d ago
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Principal Medical Writer (6-12 Month Remote Contract)

Precision Life Sciences
Medical Writer Job, Remote or Boston, MA
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Our client is seeking a Principal Medical Writer for a remote, 6-12 month contact. As a Principal Medical Writer You Will...
Senior Level
Bachelors Required
New
2d ago
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Medical Writer

Synterex
Medical Writer Job, Remote or Dedham, MA
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The medical writer will partner cross-functionally with client teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management in planning and preparation of high-quality clinical and regulatory documents. The medical writer may produce protocols, publications, study reports, investigator brochures, narratives, and module documents, according to client and agency guidelines, to support drug development under brisk timelines. Requirements Experience (5+ years) as a medical writer in the CRO/biotech/pharmaceutical field, or equivalent
Mid Level
Bachelors Preferred
New
Easy Apply
4d ago
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4.2

Medical Writer

Flywheel Partners
Medical Writer Job, Remote or Montclair, NJ
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We have an immediate opening for a full-time, entry-level Medical/Pharma/Biotech Communications Writer & Content Developer. Seeking a writer with high-energy, creativity and enthusiasm!
Full Time
Entry Level
Junior Level
Mid Level
Offers Benefits
Masters Preferred
23d ago
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4.7

Medical Writer (710655) - REMOTE

Zimmer Biomet
Medical Writer Job, Remote
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The Medical Writer is primarily responsible for preparing Clinical Evaluation Reports (CERs) for regulatory submissions and Post-market Surveillance Plan literature reviews (PSPs) for analysis of existing product clinical performance. Report preparation involves summarizing data found and drafting risk versus benefit analyses for review by Senior Medical Writer or designee. Summarize findings and draft risk versus benefit analyses and conclusions, for review by Senior Medical Writer or designee, based on clinical and post market data in accordance with European Union guidance.
Mid Level
Offers Benefits
Bachelors Required
New
3d ago
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Medical Writer (Clinical/Remote)

Propharma Group
Medical Writer Job, Remote or Durham, NC
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The Senior (Sr.) Medical Writer provides medical writing support for clients. Compiles, writes, and edits medical writing deliverables, and serves as a medical writer on inter-department and intra-department project teams with minimal supervision.
Mid Level
8d ago
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Medical Billing Client Liaison

MBMS Medical Billing and Management Services
Client Liaison Job, Remote or Boyertown, PA
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The Client Liaison acts as a resource between our business and other entities to streamline operations, develop and foster relationships, resolve issues, improve communications and generally ensure that the relationship succeeds.
Junior Level
Offers Benefits
18d ago
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Director Statistical Science - Global Medical Affairs/Payer Biometrics

Global TB
Global Director Job in Gaithersburg, MD
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Director Statistical Science, Supervisor Global Medical Affairs/Payer Biometrics The Director Statistical Science (Supervisor)
Mid Level
Professional
Executive
Masters Required
New
7d ago
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Associate Director, Medical Writer

Horizon Therapeutics
Associate Medical Director Job in Reston, VA
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Working at Horizon is more than a job - it's personal. Horizon Core Values & Competencies:
Senior Level
Professional
Executive
Masters Required
27d ago
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4.9

Director Statistical Science - Global Medical Affairs/Payer Biometrics

Astrazeneca
Global Director Job in Gaithersburg, MD
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Director Statistical Science, Supervisor - Global Medical Affairs/Payer Biometrics We hope that you are our new Director Statistical Science (Supervisor) who can join us to play an important part in our growing Global Medical Affairs/Payer Biometrics statistics group which sits within Oncology Biometrics. The Director Statistical Science (Supervisor) reports to the Head of GMA/Payer Biostatistics and will be responsible for the delivery of services to the groups two key stakeholders, GMA and Oncology Market Access and Pricing (OMAP). As a Director Statistical Science (Supervisor) you will line manage and develop a team of statisticians.
Mid Level
Professional
Executive
Masters Required
New
6d ago
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4.4

Physician - Psychiatry - *HIRING* Behavioral Health Medical Director - Full-Time

Uva Health
Medical Director Job in Manassas, VA
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UVA Health is seeking a full-time Behavioral Health Medical Director to join their growing team in Manassas, Virginia!
Full Time
Mid Level
Professional
Executive
Bachelors Required
New
6d ago
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4.8

Physician - Urgent Care - Urgent Care Medical Director (Part-Time)

Privia Medical Group
Medical Director Job in Manassas, VA
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Outstanding opportunity to join our well-established and expanding urgent care and serve as the medical director for our new office location
Professional
Executive
Doctorate Preferred
New
5d ago
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Account Liaison - Home Health and Hospice

Promedica Senior Care
Liaison Job in Silver Spring, MD
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The Account Liaison role is a performance-based health care sales position and is responsible for generating business and meeting targets from an assigned territory. The Account Liaison identifies opportunities for formal or contractual relationships with physicians, organizations and payors, as well as executes territory sales plans in coordination with operational and clinical leadership to ensure extraordinary customer service and fulfill Heartland promises.
Junior Level
Bachelors Preferred
New
1d ago
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4.9

Associate Director, Clinical Data Management Medical Coding (REMOTE)

Takeda Pharmaceutical
Associate Medical Director Job, Remote or Foxborough, MA
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Takeda Takeda fosters a collaborative and stimulating work environment, filled with opportunity and the chance to make a difference in people's lives. It is a workplace driven by integrity, one of Takeda s long-held values that extends to both the patients we serve and our employees who develop and deliver medicines. Across our company, Takeda employees bring together diverse strengths that together create a stronger whole. As one of the world s leading biopharmaceutical companies, Takeda is committed to bringing Better Health and a Brighter future to people worldwide. Clinical Data Management (CDM) at Takeda Key to Takeda's success is the Clinical Data Management Team (CDM), providing strategic planning, resourcing, execution, and oversight of clinical trial data deliverables. CDM leads the completion of clinical trial data deliverables (performed by Takeda or by vendors) from study start-up through database lock. The Associate Director, CDM Coding will manage and oversee Takeda staff, strategic partners, and vendors who conduct coding activities. They are responsible for conducting oversight of Data Management Coding activities at the program, group of programs and/or portfolio level - as performed within Takeda or by Strategic Partners, CROs, or other 3rd Party Vendors - to ensure they meet obligations as described in ICH-GCP and Takeda's Scope of Work, maximize effectiveness and maintain budgets. The Associate Director, CDM Coding provides and enables solutions for complex problem solving that align with the Takeda values. Leads clinical trial coding deliverables and activities that support Takeda regulatory commitments including submission of safety data.
Professional
Management
Executive
Doctorate Preferred
13d ago
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4.5

Medical Director/Lead Medical Director, Signaling Pathways (Early Clinical Development Oncology)

Genentech
Medical Director Job, Remote or Larkspur, CA
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The medical director will focus on clinical programs that explore the potential of a broad oncology portfolio with promising new agents including selective inhibitors of the RAS/MAPK and PI3K/AKT signaling pathways, T-cell recruiting bispecific antibodies and cancer vaccines targeting a range of cancers. The medical director will act as a clinical representative to a number of cross-functional teams responsible for the design, implementation, monitoring, analysis and reporting of studies conducted within one or more programs.
Full Time
Mid Level
Senior Level
Professional
Executive
Doctorate Preferred
New
7d ago
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4.5

Director, Computational Medical & Bioinformatics

Sanford Health
Medical Director Job, Remote or Sioux Falls, SD
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Location: Sioux Falls, SD Address: 1321 W 22nd St, Sioux Falls, SD 57105, USA Flexibility with remote work; if working remote full time, travel to Sioux Falls will be required.
Full Time
Part Time
Mid Level
Professional
Executive
Offers Benefits
Bachelors Required
30d ago
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Average Salary For a Medical Science Liaison

Based on recent jobs postings on Zippia, the average salary in the U.S. for a Medical Science Liaison is $113,905 per year or $55 per hour. The highest paying Medical Science Liaison jobs have a salary over $255,000 per year while the lowest paying Medical Science Liaison jobs pay $50,000 per year

Average Medical Science Liaison Salary
$113,000 yearly
$55 hourly
Updated July 4, 2022
$50,000
10 %
$113,000
Median
$255,000
90 %

5 Common Career Paths For a Medical Science Liaison

Manager

Managers are responsible for a specific department, function, or employee group. They oversee their assigned departments and all the employees under the department. Managers are responsible that the department they are handling is functioning well. They set the department goals and the steps they must take to achieve the goals. They are also in charge of assessing the performance of their departments and their employees. Additionally, managers are responsible for interviewing prospective candidates for department vacancies and assessing their fit to the needs of the department. Managers also set the general working environment in the department, and they are expected to ensure that their employees remain motivated.

Medical Manager

A medical manager is a health care expert primarily in charge of overseeing a particular department or office, ensuring efficiency and smooth workflow. Their responsibilities typically revolve around performing administrative tasks such as arranging schedules and appointments, handling calls and correspondence, maintaining personal records of patients, updating medical histories, and liaising with insurance companies for updates and verification. There are also instances where they must produce progress reports, delegate tasks, and train new staff, all while adhering to the hospital's policies and regulations.

Consultant

Consultants are individuals who were tapped by a company or an organization to work on a specific activity, depending on their field of expertise. They act as guides for the organization in undertaking projects that are related to their field. Consultants would usually assist organizations in planning, often giving advice when the need arises. They would, at times, take the lead in activities that involve data gathering and interpretation of data gathering results so that they can provide solid recommendations on actions that the organization may undertake. They may also guide the organization in implementing any changes brought about by their consultancy and in evaluating the effectiveness of the changes.

District Sales Manager

A district sales manager is responsible for supervising the sales team and monitoring the sales performance of the assigned district. District sales managers must have extensive knowledge about the current market trends, adjust strategies and practices as needed to improve sales operations and increase revenues. A district sales manager should also have excellent communication, leadership, and decision-making skills to provide effective techniques in attracting customers to avail of the company's offers and services, while also considering the staff's welfare.

Clinical Manager

A clinical manager is responsible for monitoring medical procedures and administrative duties to ensure the smooth flow of operations in a healthcare facility. Clinical managers manage the facility's staffing needs, evaluate budget reports, assist healthcare professionals on administering medical duties, and develop strategic procedures to optimize treatments and maximize productivity. A clinical manager enforces strict sanitary and safety regulations for everyone's strict compliance. They also need to have excellent knowledge of the medical industry to promote medical processes and provide the highest quality care.

Illustrated Career Paths For a Medical Science Liaison

Medical Science Liaison Jobs FAQs

How do I become a medical science liaison with no experience?

To become a medical science liaison with no experience, a person needs to ensure they have the right educational qualifications and develop expertise in a specific therapeutic area. This will help a person get a job as a medical science liaison without prior pharmaceutical experience.

How much do medical liaisons make?

Medical science liaisons make an average salary of $170,000 per year. However, this salary varies depending on several factors, including their employer, education, and level of experience.

Is MSL a good career?

Yes, being a medical science liaison (MSL) is a good career. This is a good career option for people in the healthcare field who want to act as a bridge between healthcare companies and physicians.

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