At Parexel, we are driven by a shared mission to improve global health. From clinical trials to regulatory consulting and market access, our clinical development solutions are rooted in a deep conviction to make a difference. Every role at Parexel contributes to the development of therapies that ultimately benefit patients. We approach our work with empathy, dedication, and a commitment to excellence.
Job Description:
Parexel is seeking a Clinical Research Associate (CRA) – FSP to join our team in Bengaluru, India. As a CRA, you will be the primary point of contact for assigned clinical sites, ensuring the integrity of study implementation and adherence to protocols. You will play a critical role in building relationships with investigators, resolving site issues, and ensuring compliance with regulatory requirements.
Key Responsibilities:
- Act as Parexel’s direct contact with assigned sites, ensuring protocol adherence and resolving site-related issues.
- Build and maintain strong relationships with investigators and site staff.
- Facilitate site access to study systems and ensure compliance with training requirements.
- Conduct on-site visits, including Qualification and Initiation visits, and address site-specific challenges.
- Evaluate site performance, recruitment plans, and compliance, providing recommendations for improvement.
- Monitor data quality and integrity, ensuring timely resolution of issues.
- Maintain and update Clinical Trial Management Systems (CTMS) and Trial Master Files (TMF).
- Ensure sites are audit and inspection-ready, complying with ICH-GCP guidelines and local regulations.
- Collaborate with cross-functional teams to meet project goals and timelines.
- Provide training and guidance to site staff as needed.
- Manage study supplies, site payments, and documentation.
Skills and Qualifications:
- Education: Degree in biological sciences, pharmacy, nursing, or a related field (or equivalent experience).
- Experience: Site management or clinical research experience with a strong understanding of clinical trial methodology.
- Problem-Solving: Strong analytical and problem-solving skills.
- Communication: Excellent interpersonal, verbal, and written communication skills.
- Technical Proficiency: Familiarity with Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and MS Office tools.
- Travel: Willingness to travel extensively as required.
- Attention to Detail: High level of accuracy and attention to detail.
- Teamwork: Ability to work effectively in a matrix environment and foster collaboration.
Why Join Parexel?
- Impactful Work: Contribute to the development of therapies that improve patient lives.
- Professional Growth: Opportunities to develop expertise and advance your career.
- Collaborative Culture: Work in a supportive, results-oriented environment that values teamwork and innovation.
- Global Reach: Be part of a global organization with a presence in over 50 countries.
How to Apply:
If you are passionate about clinical research and meet the qualifications, we encourage you to apply for the Clinical Research Associate (CRA) – FSP position at Parexel. Click the link below to submit your application:
