Parexel Hiring Clinical Operations Assistant
- Explore a Career in Clinical Research: Join Parexel as a Clinical Operations Assistant
- Key Responsibilities
- Central File & Documentation Management
- Clinical Trial Support & Tracking
- Administrative & Site Coordination
- Required Qualifications
- Educational Background
- Skills & Experience
- Why Join Parexel?
- Apply Now
- Summary Table
Clinical Research Assistant Jobs for Life Sciences Graduates in Bengaluru
Apply for Clinical Operations Assistant jobs in Bengaluru. Life Sciences or Pharmacy graduates with clinical research knowledge preferred. 1–2 years experience required
Explore a Career in Clinical Research: Join Parexel as a Clinical Operations Assistant
Are you a life sciences graduate with a passion for clinical trials and research operations? Parexel, a leading global Clinical Research Organization (CRO), is inviting applications for the position of Clinical Operations Assistant (COA) in Bengaluru, India. This role offers the perfect platform for professionals with 1 to 2 years of experience to gain deep exposure to clinical trial management systems and document control protocols in a dynamic and supportive environment.
This position is open to candidates with educational backgrounds in Biological Sciences, Pharmacy, Nursing, or any health-related discipline. Candidates with prior experience in CROs or the life sciences industry are highly encouraged to apply.
Key Responsibilities
Central File & Documentation Management
- Track, scan, label, and upload clinical documents to the Central File (CF) and Work In Progress (WIP) areas in line with internal SOPs.
- Archive and file wet-ink paper documents according to the Central File Maintenance Plan (CFMP).
- Conduct photocopying, printing, and document retrieval as needed.
- Perform routine quality control checks to ensure document accuracy and compliance.
Clinical Trial Support & Tracking
- Maintain study-specific trackers and Clinical Trial Management Systems (CTMS).
- Monitor reporting systems and timelines, ensuring compliance with annual reporting, site safety updates, and regulatory obligations.
- Organize translations and support internal approval workflows through platforms like Oracle.
Administrative & Site Coordination
- Coordinate courier shipments, internal signature collections, and invoice/payment processing.
- Assist with document collection and coordination for clinical sites in Japan.
Required Qualifications
Educational Background
- Bachelor’s degree in Biological Sciences, Pharmacy, Nursing, or other health-related discipline
- Equivalent nursing qualifications or relevant experience also considered
Skills & Experience
- 1–2 years of relevant experience in clinical research, preferably in CROs or life sciences
- Understanding of clinical trial protocols, site operations, and regulatory documentation
- Strong communication, time management, and organizational skills
- Familiarity with systems like CTMS, Impact Harmony, and electronic document management tools
Why Join Parexel?
Parexel offers a supportive environment with opportunities to grow across global clinical research operations. Employees benefit from structured career development programs like APEX, which provide fast-tracked growth from administrative roles into clinical functions.
Apply Now
Ready to build a clinical research career with one of the world’s most trusted CROs?
👉 Apply Here
Summary Table
| Company Name | Parexel |
|---|---|
| Current Vacancies in Departments | Clinical Operations Assistant |
| Required Education | Bachelor’s in Life Sciences, Pharmacy, Nursing, or related field |
| Experience Required | 1–2 years in clinical research |
To apply for this job please visit jobs.parexel.com.
