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 Now
Apply Now
• 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 Now
Apply Now