Clinical Research Associate, Level II – Functional Service Provider
Job Description:
- Performs and coordinates all aspects of the clinical monitoring and site management process
- Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation
- Ensures audit readiness
- Develops collaborative relationships with investigational sites
- Conducts monitoring tasks in accordance with the approved monitoring plan
Requirements:
- Must have a Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification
- CRA Level II Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1+ years as a clinical research monitor)
- Valid driver's license where applicable
- Proven clinical monitoring skills, ideal candidates will have monitoring experience with oncology, HIV, respiratory and or vaccine/flu
- Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
- Ability to manage Risk Based Monitoring concepts and processes
Benefits:
- A choice of national medical and dental plans, and a national vision plan, including health incentive programs
- Employee assistance and family support programs, including commuter benefits and tuition reimbursement
- At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
- Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
- Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
Apply tot his job Apply To this Job