Phone Support Specialist- Customer Service- Remote
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$63k-89k yearly est.60d+ ago
Phone Support Specialist- Customer Service- Remote
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Qualified customer service professionals will be responsible for providing phone support for clinical trial participants and clinical trial site staff. The **_Clinical Phone Support Specialist_** role will allow you to utilize your customer service experience to support our customer with clinical trials. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$64k-90k yearly est.60d+ ago
US Oxbryta (Sickle Cell Disease) Director: Omnichannel Patient Marketing
Pfizer's Bold Moves and Values has led to a prioritization of enabling Digital-First patient engagements.$144.9k-241.5k yearly14d ago
Insurance Billing & Coding Specialist
Job Description Full or part time Insurance Billing & Coding Specialist needed at our office. Baxter Eye Care has been serving The Woodlands with quality eye care and personal friendly service since 1981. Baxter Eye Care also provides vision therapy for extraocular muscle imbalances, focusing difficulties, and tracking inefficiences.$31k-39k yearly est.3d ago
Phone Support Specialist- Customer Service- Remote
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Qualified customer service professionals will be responsible for providing phone support for clinical trial participants and clinical trial site staff. The **_Clinical Phone Support Specialist_** role will allow you to utilize your customer service experience to support our customer with clinical trials. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$53k-79k yearly est.60d+ ago
Phone Support Specialist- Customer Service- Remote
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. Qualified customer service professionals will be responsible for providing phone support for clinical trial participants and clinical trial site staff. The **_Clinical Phone Support Specialist_** role will allow you to utilize your customer service experience to support our customer with clinical trials. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$55k-75k yearly est.60d+ ago
Phone Support Specialist- Customer Service- Remote
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. No matter your role, everyone at IQVIA, including our colleagues at Q Solutions, contributes to our shared goal of improving human health.$57k-85k yearly est.60d+ ago
Packaging Operator, Part -Time 2nd shift - Shift differential + $1,000 Sign On Bonus!! Benefits day one!
No matter your role at Baxter, your work makes a positive impact on people around the world. Summary The Packaging Operator works within the Finishing/Packaging Complex. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. * Required to maintain attendance in accordance with the Bloomington Attendance Policy At Baxter, we are deeply connected by our mission.$18.7 hourly5d ago
Controls Engineer Intern
We are looking for a Controls Engineering Intern to join our team in our Walled Lake, MI office. The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. *Work directly with Leidos software engineers.$37.1k-57k yearly8d ago
Contract Senior Ophthalmology Clinical Research Associate, West Coast - IQVIA Biotech
Help create a healthier world: START RIGHT HERE AT IQVIA.
Our clinical monitoring team is seeking an experienced CRA with at least 4 years of onsite experience and 2 years of Ophthalmology monitoring experience. Cell and Gene Therapy is preferred but not required. This is a part-time contract assignment.
BASIC FUNCTIONS:
Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA t0 ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also serve in the Lead CRA role.
ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:
Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
Collaborates with the ISS department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISS and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.Trains site staff on the EDC system and verifies site computer system.Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.Assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.Documents accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required.Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries.May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.Assists with, and attends, Investigator Meetings for assigned studies.Authorized to request site audits due to data integrity concerns.Attends study-related, company, departmental, and external meetings, as required.Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.Ensures all study deliverables are completed per IQVIA Biotech and study timelines Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.Serves as mentor for junior CRAs and those new to the company and/or study.Performs other duties, as requested.
KNOWLEDGE, SKILLS AND ABILITIES:
Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.Four+ years of oncology experience and/or medical device.Experience in monitoring and/or coordinating clinical trials required.Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.Demonstrated ability to form strong functional relationships.Excellent, presentation, organizational and interpersonal skills.Ability to interact with all levels of staff to coordinate/execute study activities.Ability to handle several priorities within multiple, complex trials.Ability to reason independently and recommend specific solutions in clinical settings.Ability to work independently, prioritize, and work within a matrix team environment.Ability to mentor other CRAs and co-monitor, as required.Knowledge of electronic data capture including basic data processing functions.Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.Able to qualify for a major credit card, rent an automobile For the Technical CTM role, the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more.
PHYSICAL REQUIREMENTS:
Very limited physical effort required to perform normal job duties Extensive use of telephone and face-to-face communication requiring accurate perception of speech Extensive use of keyboard requiring repetitive motion of fingers Regular sitting for extended periods of time
MINIMUM RECRUITMENT STANDARDS:
BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience.Prior Clinical Research Organization (CRO) experience preferred.Prior project team leadership experience preferred.Working knowledge of budget management preferred.Must be able to travel domestically and internationally approximately 65%-85%.Valid driver's license
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IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
Colorado/California/Washington
state Pay Transparency : The salary range for this role is $67,300 - $84,000.The actual salary will vary based on factors like candidate qualifications and competencies. Certain roles are eligible for annual bonus, sales incentives and/or stock. Benefits may include healthcare, retirement, paid time off, and more.$67.3k-84k yearly11d ago
Jr. Controls Engineer
Leidos, is seeking Controls Engineers to join our team in our Walled Lake, MI office The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary.$53.3k-82k yearly11d ago
Omnichannel Patient Marketing Director
The Omnichannel Patient Marketing Director will be responsible for developing, implementing and evaluating promotional materials, programs and activities targeted at patients and caregivers living with Sickle Cell Disease. Pfizer's Bold Moves and Values has led to a prioritization of enabling Digital-First patient engagements. The Omnichannel Patient Marketing Director will serve a critical lead role for the US Sickle Cell Franchise to ensure short and long-term success of Oxbryta and the SCD portfolio.$144.9k-241.5k yearly13d ago
Omnichannel Patient Marketing Director
The Omnichannel Patient Marketing Director will be responsible for developing, implementing and evaluating promotional materials, programs and activities targeted at patients and caregivers living with Sickle Cell Disease. Pfizer's Bold Moves and Values has led to a prioritization of enabling Digital-First patient engagements. The Omnichannel Patient Marketing Director will serve a critical lead role for the US Sickle Cell Franchise to ensure short and long-term success of Oxbryta and the SCD portfolio.$144.9k-241.5k yearly13d ago
US Oxbryta (Sickle Cell Disease) Director: Omnichannel Patient Marketing
Pfizer's Bold Moves and Values has led to a prioritization of enabling Digital-First patient engagements.$144.9k-241.5k yearly14d ago
US Oxbryta (Sickle Cell Disease) Director: Omnichannel Patient Marketing
Pfizer's Bold Moves and Values has led to a prioritization of enabling Digital-First patient engagements.$144.9k-241.5k yearly14d ago
Contract Senior Ophthalmology Clinical Research Associate, West Coast - IQVIA Biotech
+ Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts. **Help create a healthier world:** **START RIGHT HERE AT IQVIA. + Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested. Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. + Ensures all study deliverables are completed per IQVIA B Prepares monitoring reports and letters per the timelines defined in IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.$67.3k-84k yearly38d ago
Vascular Clinical Assistant- Novasyte
CAT1 IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human he$26k-40k yearly est.10d ago
