Requirements:
- Educational Qualification:Sc, MSc, D.Pharm , B Pharm, M Pharm, Biotechnology, Microbiology and any other degree in life sciences candidates can apply.
- Strong interest in clinical research and a desire to learn and develop within the field.
- Good organizational skills and attention to detail.
- Excellent interpersonal and communication skills
- Ability to work effectively both independently and as part of a team
- Flexibility to adapt to changing priorities and responsibilities.
- Candidates with experience will have a preference
Job Description:
- Strong Knowledge of ICH-GCP E6 R2 guidelines and other Indian and international regulatory guidelines
- To facilitate and coordinate the all daily clinical research trial activities, for assigned projects
- Support in managing study visits, following study protocols and guidelines.
- Help with logistics such as ordering and maintaining supplies needed for the study
- Assist in maintaining study-related documentation, conduct reminder calls, manage study subject’s reimbursements, AE & SAE reporting, Source Document Maintenance
- Assist in Investigator Site File management, IP accountability & CRF Completion, completion of all study logs
- Working with the monitors (CRA’s) during their monitoring visits and participate in data verification, source document verification (SDV), and quality control activities.
- Maintain effective communication with study team members, investigators, and study participants
- Attend study team meetings, providing updates on study progress and challenges.
- Ensure adherence to regulatory requirements and guidelines throughout the study.
- Assist in maintaining accurate and up-to-date regulatory documents
- Stay informed about industry trends and advancements in clinical research.
Job Type: Full Time/Day shift (3-6 months on-site training)
Salary: Stipend as per industry norms
