Clinical Research Job At Parexel | Apply Now
If you’re looking to grow in Clinical Research Jobs and advance within leading Pharma Careers, the Clinical Research Associate II role at Parexel offers a powerful opportunity to work on global studies that directly impact patient care. Located in Bengaluru, India, this role supports meaningful clinical development while strengthening your professional journey through Parexel Careers, known worldwide for excellence, integrity, and patient-first innovation.
Job Details:
- Job Title: Clinical Research Associate II
- Primary Location: India, Bengaluru
About the Company:
Parexel is one of the world’s leading Clinical Research Organizations (CROs), offering global opportunities for individuals seeking Clinical Research Jobs and long-term Pharma Careers. Through its people-first culture and commitment to innovation, Parexel Careers attract professionals who want to contribute to the advancement of healthcare worldwide.
Job Description:
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. This role involves building relationships with the site, ensuring site performance, development of robust patient recruitment strategies, compliance assessment, and problem solving to address site issues.
The Clinical Research Associate will oversee trial conduct at designated sites, ensure participant safety, evaluate data integrity, and evaluate site staff training. This role also entails developing patient recruitment strategies, promoting positive relationships, and ensuring compliance with protocols and regulatory requirements. Additional tasks may include working under a Clinical Operations Leader and supporting protocol amendments.
Key Responsibilities In Clinical Research Jobs:
- Act as PAREXEL’s direct contact with assigned sites, ensuring study integrity and protocol adherence.
- Build relationships with investigators and site staff.
- Ensure sites have access to relevant study systems and are compliant with training requirements.
- Evaluate on-site staff assignment and address any deficiencies.
- Resolve site-related issues, ensuring data quality and integrity.
- Participate in investigator meetings and audits.
- Evaluate site recruitment plans and provide strategic improvements.
- Conduct on-site visits and remote contacts as needed.
- Ensure compliance with ICH-GCP and local regulations.
- Maintain project scope understanding and strive for high-quality delivery.
Qualifications Required For Clinical Research jobs:
Education:
-
Degree in biological science, pharmacy, health-related discipline OR equivalent nursing qualification.
Skills:
- Sound problem-solving skills and independence in work.
- Advanced presentation and client-focused approach.
- Ability to prioritize tasks and work in a team environment.
- Strong computer skills, including CTMS and MS-Office proficiency.
- Exceptional communication skills and attention to detail.
- Willingness to travel as required.
Knowledge and Experience:
Site Management experience or equivalent in clinical research, with knowledge of clinical trials methodology and terminology.
