CLINICAL RESEARCH EXECUTIVE

As a Clinical Research Coordinator, your role involves coordinating study activities and timelines, scheduling participant visits, and ensuring compliance with regulatory requirements. You will be responsible for coordinating study procedures such as laboratory tests and imaging studies. Key Responsibilities: - Support data analysis of research data, including statistical analysis and interpretation of study findings. - Assist in preparing study-related documentation such as research protocols, informed consent forms, and regulatory submissions. - Aid in the preparation of study reports, abstracts, and manuscripts for publication. - Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and institutional policies throughout the study. - Collaborate with interdisciplinary teams to ensure the smooth conduct of clinical research studies. - Participate in ongoing training and educational activities related to clinical research. - Uphold ethical standards in the conduct of clinical research, protecting the rights and welfare of research participants and maintaining confidentiality of study data. Qualifications: - BDS, MSc in Biotechnology, Microbiology, or Biochemistry - B. Pharm, M. Pharm, or Pharm D - MSc or BSc in Life Sciences such as Bioinformatics or Biomedical Engineering The company is located in Kochi, Kerala, and the job type is full-time with a morning shift schedule. The ideal candidate would have a Master's degree and up to 1 year of relevant work experience. This position is suitable for freshers or individuals looking for an internship opportunity in the field of clinical research. As a Clinical Research Coordinator, your role involves coordinating study activities and timelines, scheduling participant visits, and ensuring compliance with regulatory requirements. You will be responsible for coordinating study procedures such as laboratory tests and imaging studies. Key Responsibilities: - Support data analysis of research data, including statistical analysis and interpretation of study findings. - Assist in preparing study-related documentation such as research protocols, informed consent forms, and regulatory submissions. - Aid in the preparation of study reports, abstracts, and manuscripts for publication. - Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and institutional policies throughout the study. - Collaborate with interdisciplinary teams to ensure the smooth conduct of clinical research studies. - Participate in ongoing training and educational activities related to clinical research. - Uphold ethical standards in the conduct of clinical research, protecting the rights and welfare of research participants and maintaining confidentiality of study data. Qualifications: - BDS, MSc in Biotechnology, Microbiology, or Biochemistry - B. Pharm, M. Pharm, or Pharm D - MSc or BSc in Life Sciences such as Bioinformatics or Biomedical Engineering The company is located in Kochi, Kerala, and the job type is full-time with a morning shift schedule. The ideal candidate would have a Master's degree and up to 1 year of relevant work experience. This position is suitable for freshers or individuals looking for an internship opportunity in the field of clinical research.