Clinical Trial Associate Jobs at Dr. Reddy’s, BSc, MSc & Diploma Candidates Apply
Clinical Trial Associate
Location: Hyderabad, Telangana, India
About the job
Company Description
Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000-plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait.
Job Description
Job Summary
The Clinical Trial Associate (CTA) supports clinical studies and the Clinical Operations Department, in managing various administrative tasks such as generation of agenda and minutes, maintaining study tracking, filing and quality reviews, as well as participating in process improvement initiatives across the departments.
Roles & Responsibilities
- Provide general administrative support to the Clinical Operations Department and assistance to the study team(s).
- Assist in the production of presentations as needed for project, departmental, and/or business development.
- Assists the team with Sponsor oversight, study-specific documentation review and QC, including review of ICF, study plans, study reference manuals, e-CRF, etc.
- Assist with creation and maintenance of study metrics trackers, tools, and reports.
- Assist in coordination and tracking of Investigator and third-party payments.
- Ensures required study documents are submitted to the eTMF.
- Assists the team with Sponsor oversight of eTMFs periodic audit and findings resolution.
- Assist the team in executing clinical monitoring oversight.
- Assists with customization of CDA, clinical site contracts & budgets, when applicable.
- Assist the clinical team with Investigator Meeting coordination, activities preparation, and generate meeting minutes.
- Coordinate document translation, if required.
- May participate in training CRO teams and in the onboarding of new CRO team members.
- May contact clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements, etc. when requested).
- Attend internal and external team meetings/teleconferences and generate meeting agenda and minutes when needed.
- Other duties may be assigned as required.
- If required, the candidate should be willing to travel as needed.
Qualifications
- Educational qualification: Graduate/Master’s degree in Pharmacy, Life Science, Biology, Biotechnology, Biochemistry, or Diploma in Clinical Research
- Minimum work experience: 1 – 3 years of Clinical Trial experience
Skills & Attributes
Technical Skills
- Experience in Clinical Trial operations.
- Proficiency in conducting Market research and analysis.
- Knowledge of regulatory requirements and guidelines such as Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines.
- Ability to evaluate medical research data and proficient knowledge of medical terminology.
- Proficiency in using EDC systems for data collection and management in clinical trials.
- Strong MS Office skills.
Behavioral Skills
- Excellent communication, negotiation, and interpersonal skills.
- Excellent project management skills.
- Strong analytical and problem-solving abilities with a keen eye for detail.
- Result-oriented and passionate about delivering value.
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Keywords: Clinical Trial Associate, Dr. Reddy’s Laboratories, Clinical Trial Operations, Good Clinical Practice, Clinical Research, Hyderabad, Telangana, India. Clinical Trial Associate Jobs at Dr. Reddy’s, BSc, MSc & Diploma Candidates Apply. Please ensure you are subscribed to the Biotecnika Times Newsletter and our YouTube channel to be notified of the latest industry news. Follow us on social media like Twitter, Telegram, Facebook