Dr. Reddy’s Laboratories Hiring Clinical Trial Associate Hyderabad

Dr. Reddy’s Laboratories is seeking a dedicated Clinical Trial Associate to join their team in Hyderabad. This full-time, on-site position offers a fantastic opportunity to work in a dynamic environment and contribute to impactful clinical studies.

Job Description

Job Summary

As a Clinical Trial Associate (CTA) at Dr. Reddy’s Laboratories, you will play a crucial role in supporting clinical studies and the Clinical Operations Department. Your responsibilities will include managing various administrative tasks, maintaining study tracking, filing, and quality reviews, and participating in process improvement initiatives across 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 co-ordination 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 customisation of CDA, clinical site contracts & budgets, when applicable.
• Assist the clinical team with Investigator Meeting coordination, activities preparation and generate meeting minutes.
• Co-ordinate document translation, if required.
• May participate in training CRO teams and in the on-boarding of new CRO team members.
• May contact clinical sites for specific requests (e.g., enrolment updates, missing documentation, meeting arrangements, etc. when requested).
• Attends internal and external team meetings/teleconferences and generate meeting agenda and minutes when needed.
• Other duties may be assigned as required.

Qualifications

Educational Qualification:

• Graduate/Master’s degree in Pharmacy, Life Science, Biology, Biotechnology, Biochemistry, or Diploma in Clinical Research.

Experience:

• 1-3 years of Clinical Trial experience.

Skills & Attributes

Technical Skills:

• Experience in Clinical Trial operations.
• Proficiency in market research and analysis.
• Knowledge of regulatory requirements and guidelines such as GCP and 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.
• Strong project management skills.
• Analytical and problem-solving abilities with a keen eye for detail.
• Result-oriented and passionate about delivering value.

Apply Now

If you meet the qualifications and are excited about the opportunity to work with Dr. Reddy’s Laboratories, apply online via LinkedIn.