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Clinical Research
Pharama company
Chennai, Tamil Nadu, IndiaFresher22m agovia LinkedIn
About the Role
This is a full-time, on-site Clinical Research role based in Chennai. The role involves supporting the design, planning, and execution of clinical trials in coordination with cross-functional teams.
Key Responsibilities
- Preparing study documents
- Assisting with protocol development
- Managing study data
- Maintaining accurate trial records
- Monitoring participant safety
- Ensuring adherence to regulatory and ethical guidelines
- Coordinating with investigators, site staff, and internal stakeholders
- Contributing to data analysis support
- Report preparation
- Continuous improvement of research processes
Qualifications
- Strong understanding of clinical research processes, Good Clinical Practice (GCP), and relevant regulatory guidelines.
- Ability to manage documentation, maintain accurate study records, and support data collection and data quality activities.
- Effective communication and collaboration skills for working with investigators, site personnel, and internal teams.
- Attention to detail, organizational skills, and the ability to prioritize tasks in a fast-paced research environment.
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field.
- Prior experience or internship in clinical research, clinical operations, or pharmacovigilance is an advantage.
- Proficiency in basic computer applications and familiarity with clinical trial management or data capture systems is beneficial.
- Commitment to ethical conduct, participant safety, and continuous learning in clinical research.