Clinical medical / safety
Location
Columbus, OH | United States
Job description
As an individual contributor, with guidance from manager/team, functions to support medical safety team by collecting, assessing, processing adverse events for clinical or post-marketed products in compliance with applicable regulations, guidelines, researching, assessing and summarizing nutrition and medical information as well as safety issues concerning foods or products and, by supporting clinical study teams with safety related aspects and issues.
Responsibilities: - Collecting, assessing and processing adverse event information in a compliant and timely manner in order to meet applicable regulatory requirements.
- Coding cases using appropriate dictionary, searching and inputting data in electronic databases.
- Generating, tracking and resolving adverse event follow-up/distribution correspondence; managing adverse event reports from initial cases and follow-up.
- Assisting in the completion of MSS related analyses, reports, and/or projects as assigned, e.g., ingredient and finished product assessments and/or medical safety assessments.
- Presenting MSS related analyses, reports, and/or assessments orally and/or in writing within the department.
- Researching, organizing and assimilating clinical, safety, and/or toxicology information to support medical safety assessments, clinical study related safety reports, safety fact sheets and chemical approvals.
- Assisting in the generation of medical justification content reviews/templates for MSS.
Skills: - 1-3 years related experience (Research Coordinator, Clinical Monitor, etc.)
- Clinical knowledge to apply to adverse events
- Data collection and/or medical/product assessments
- Computer proficiency (Windows, Word, Excel)
- Able to present case data, medical and scientific data orally and in writing.
Education: - Associates or Bachelor’s degree in Healthcare or Science.
Schedule: - Onsite 4 day and 1 work from home day.
Hours: - 8:30-5:00, M-F (1 work from home day per week)
Pay: If you are interested, please email your resume to cpepe @ actalentservices.com to schedule a phone interview! About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email
[email protected] for other accommodation options.
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