Jobs For Clinical Research Associate

JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines. 3....

Role DescriptionThis is a full-time on-site role for a Senior Clinical Research Coordinator, located in Chennai. The Clinical Research Coordinator will be responsible for managing clinical trials, ensuring informed consent is obtained, and adhering to research protocols. The role involves coordinating and overseeing day-to-day research activities,...

Job Description Title: Clinical Research AssociateDate: Jun 6, 2025Location: Not ApplicableCompany: Sun Pharma Laboratories LtdJob location: ChennaiYOUR TASKS AND RESPONSIBILITIES:Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and...

**Job Description**: Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study...

**Role**: Research Associate (Web Research) **Degree**: BSc. or MSc. **Discipline**: Any of the following - Biochemistry, Microbiology, Biotechnology To research various web sources and databases to capture data based on the project requirements which include web research, reviewing scientific literature, industry associations, clinical trials, clinical...

Job Description Job Location: ChennaiYOUR TASKS AND RESPONSIBILITIES:Perform site feasibility, identify potential investigator, negotiate study budget with potential investigators, finalization of investigators, sites, and execution of CDA and study-related contracts Preparation and submission of study documents for EC permission for respective study...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collecting and...

JOB DETAILS 1.writing drug trial methodologies (procedures)2.identifying and briefing appropriate trial investigators (clinicians) 3.setting up and disbanding trial study centres 4.designing trial materials and supplying study centres with sufficient quantities 5.providing clinicians with instructions on how to conduct the trials 6.collecting and...

Should Complete Msc. Neuro Science - Knowledge of medical and clinical research terminology and processes. - Ability to follow and provide critical feedback on the investigational plan. - Ability to develop study related budgets, contracts, and patient consent documents. - Regulations associated with the conduct of clinical trials and other related research...

**Job description** **Degree**: BSc. or MSc. **Discipline**: Any of the following - Biochemistry, Microbiology, Biotechnology, Bioinformatics, Biomedical Sciences, Genetics, Genomics, Molecular Biology **Role**: Research Associate (Web Research) To research various web sources and identify data as per the project requirements which includes web research,...