Senior Safety Associate III - Cambridge, United States - Randstad USA

Randstad USA Cambridge, United States

3 weeks ago

Freelance, Full time

Description

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. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team

location: Cambridge, Massachusetts
job type: Contract
salary: $ per hour
work hours: 9 to 5
education: Bachelors

responsibilities:
The Senior Safety Associate III will be responsible for supporting Global Case Management with ICSR quality review, controlled document updates and creation, training material edits and creation and associated tasks, and other case processing oversight activities as delegated. The Senior Safety Associate III supports the Case Processing Oversight and ICSR Processes and GCM Systems teams and is responsible for ensuring AE case processing is compliant with regulatory requirements and corporate and departmental procedures.

Perform quality review of ICSRs
Monitor case processing workflow for vendors and escalate cases at risk of missing timelines.
Perform review and updates in controlled documents.
Recording meeting minutes and team notes.
Participate in testing and conference room pilots for Global Safety Database (GSD) upgrade project.
Support other tasks as assigned by manager.
qualifications:
- Bachelor's Degree in nursing, pharmacy, or other health care related profession or life sciences
- Must have direct experience with end-to-end Case Processing (data entry and quality review) of both Clinical Trial and Post-marketing ICSRs
- Advanced proficiency in Microsoft Office applications
- Exceptional organizational skills and attention to detail
- Ability to successfully and efficiently multi-task
- Excellent communication skills (written and verbal)
- Knowledge of common safety database systems
- Ability to work collaboratively in a team environment
  skills: Pharmacovigilance, MS-WORD, MS-EXCEL, MS-Powerpoint, ICSR (Individual Case Study Report)
  
  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.
  
  At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact
  
  Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
  
  Applications accepted on ongoing basis until filled.

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