Biomedical jobs in Kochi, Kerala

Job description:

. Coordinating study activities and timelines, scheduling participant visits, coordinating study procedures (e.g., laboratory tests, imaging studies), and ensuring compliance with regulatory requirements.

· Data Analysis: Support analysis of research data, including statistical analysis and interpretation of study findings.

· Documentation and Reporting: Assisting in the preparation of study-related documentation, including research protocols, informed consent forms, and regulatory submissions. Additionally, helping in the preparation of study reports, abstracts, and manuscripts for publication.

· Regulatory Compliance: Ensuring compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and institutional policies throughout the conduct of the study. This includes maintaining study documentation, conducting internal audits, and participating in regulatory inspections as needed.

· Collaboration: Collaborating with interdisciplinary teams, including physicians, nurses, laboratory personnel, and statisticians, to ensure the smooth conduct of clinical research studies. Additionally, communicating study progress and findings to stakeholders such as investigators, sponsors, and regulatory agencies.

· Training and Education: Participating in ongoing training and educational activities related to clinical research, including protocol-specific training, GCP training, and professional development opportunities.

· Adherence to Ethical Standards: Upholding ethical standards in the conduct of clinical research, including protecting the rights and welfare of research participants and maintaining confidentiality of study data.

Required Experience, Skills and Qualifications

BDS, MSc Biotechnology, Microbiology, Biochemistry B. Pharm, M. Pharm, Pharm D. MSc. Bsc. LifeScience: Bioinformatics, Biomedical Engineering ect.Job Types: Full-time, Internship

Pay: ₹25,000.00 per month

Work Location: In person