job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now!
location: Waltham, Massachusetts
job type: Contract
salary: $30.43 - 35.80 per hour
work hours: 9 to 5
- Responsible for the collection, data entry, routing, follow-up, and timely reporting/submission of safety information (including expedited and aggregate reports) related to drug products from a variety of sources (clinical trial, spontaneous, literature) in compliance with SOPs and regional & international regulations.
- This position is especially important in light of the approval and marketing of products and the number and diversity of clinical trials. Authorities conduct periodic, detailed audits to ensure integrity of AE processing, thoroughness of documentation, accuracy of results, and timeliness of reports.
- This position is also responsible for self-initiated quality review within each distinct process step.
qualifications: Education & Qualifications:
- 3 - 6 Years
- Bachelors Degree in a Scientific Discipline
skills: SOP, CTMS (Clinical Trial Management Systems), Clinical Trial Supply Strategy
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.