C
Clinical Research Associate
Cambridge, Massachusetts, United States · Contract
Be the first to apply
- Experience
- 3+ yrs
- Salary
- —
- Openings
- 1
- Posted
- 1 week ago
- Work mode
- In office
- Education
- Bachelor's in Life Sciences, Nursing, Pharmacy or related field
- Resume
- Required to apply
Where you'll work
Job description
About the Role
Join a rapidly expanding biotechnology company focused on pioneering neurological therapies as a Clinical Research Associate (CRA). This position offers an opportunity to contribute significantly to clinical trial success and ultimately improve patient outcomes in neuroscience.
Key Responsibilities
- Lead site initiation, monitoring, and close-out visits ensuring adherence to highest quality standards in clinical trials.
- Thoroughly review and validate clinical study data for accuracy and completeness.
- Coordinate effectively with site personnel and multidisciplinary teams to address study challenges and maintain trial progress.
- Detect and promptly report protocol violations, safety issues, or data inconsistencies.
Candidate Requirements
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or related discipline; advanced degrees are advantageous.
- Minimum three years of experience in clinical research associate roles or site monitoring.
- Comprehensive understanding of ICH-GCP guidelines and FDA regulatory standards.
- Strong communication, organizational, and analytical problem-solving abilities.
- Flexibility to travel frequently, potentially up to 50-75% of the time.
Preferred Qualifications
- Experience conducting clinical trials in central nervous system (CNS) or rare diseases is highly desirable.
Benefits
Competitive benefits package available from the first day of employment.
Skills
Work styles they’re looking for
Problem Solving
Communication Skills
Organizational Skills
Travel Flexibility