Clinical Research Coordinator (CRC)
Clinimed LifeSciences · Guwahati · onsite · Posted 65d ago
Undisclosed1–2 yrsfulltimeSourced from
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About this role
Job Summary
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
We require experienced Clinical Research Coordinator (CRC) for the Clinical Trial Department in Guwahati, Rourkela, and Kolkata locations.
GCP Training The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants.
We arrange the GCP Training for all our employees. GCP training provides you with in-depth knowledge on the topic on regulatory requirements by international inspection organisations. There are different ways of delivering GCP training, ranging from a traditional approach through to a more modern risk-based approach. CliniMed organized GCP training has evolved from classroom-based instructor led training to eLearning (computer-based modules) supported by case studies, scenarios, and knowledge tests. These GCP training programs can be provided by internal training departments or by external providers. Functional GCP training, covering targeted areas, is mainly provided internally by CliniMed.
Job Description Job Title: Experienced Clinical Research Coordinator (CRC) We require experienced Clinical Research Coordinator (CRC) for Clinical Trial Department in Guwahati, Rourkela, and Kolkata locations.
Roles and Responsibilities - Conducting clinical trials
- Getting CDA signed from investigator and subsequently filling Feasibility forms
- Maintaining documentation for the patients enrolled in clinical trial
- Counselling patients
- Assisting investigators in informed consent process
- Handling lab sample packaging and arranging shipments
- Making electronic data (e-CRF) entries along with source documents
- Analyzing and reporting protocol deviations
- Reporting AE or SAE if needed
- Good knowledge of Good Clinical Practices (GCP) and ICH Guidelines
- MS Office
- Good communication skills in English, Hindi, Assamese and Oriya
- B. Pharm / M. Pharm / B.Sc. (Bioscience) / M.Sc. in Biotechnology, Microbiology, Molecular Biology etc.
Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
Sourced from naukri
Skills
case studiesclinical researchclinical trialstraining programsgoogle cloud platformbiologymolecular biologyInstructorOriyaAssameseBiotechnologyMicrobiologyE-learningJQueryResearch
About Clinimed LifeSciences
Clinimed LifeSciences
About
CliniMed LifeSciences Pvt. Ltd. is a clinical research and life sciences organization specializing in clinical trials, pharmacovigilance, and data management. The company also provides training programs in bioinformatics, drug development, and regulatory affairs, supporting pharmaceutical and biotech firms. With a focus on innovation, compliance, and global standards, CliniMed contributes to advancing healthcare research and improving patient outcomes.
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