Clinical Research associate-Reputed Medical

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...

Eligibility: - Graduate / Post Graduates in Life Sciences/ Pharmacy from a reputed institute - Prior knowledge of the conduct of Clinical Trials, - Phases of Clinical trials and - Thorough Knowledge of ICH-GCP and other regulatory guidelines. Roles and Responsibilities: - Prepare the Database of the Investigators at the place assigned to you. - Interact...

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....

**Job Title**: Clinical Research Associate (Fresher) **Company**: ClinoGenesis Research Organisation **Location**: Hyderbad **Employment Type**: Full-time **Job Overview**: We are currently hiring **fresh graduates** for the role of **Clinical Research Associate (CRA)**. This entry-level opportunity is perfect for individuals looking to build a career in...

JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial. 3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion. 4) Liaise with ethics...

Job OverviewAs a key member of our team, you will be responsible for creating and writing trial protocols that align with the goals of our organization. These protocols will then be presented to our steering committee for approval.We are seeking an individual who can identify, evaluate, and establish trial sites that meet our high standards. Once a site is...

**MakroCare** is an Expert Strategic Development and Commercialization Global Partner for Pharmaceutical,Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a NewDimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,Medical/Scientific Support and Emerging Region Expansion **Job...

**MakroCare** is an Expert Strategic Development and Commercialization Global Partner for Pharmaceutical,- Biotechnology and Medical Device industries. Our Experience, Programs and Processes bring a New- Dimension to Development Strategy, Regulatory/Risk Planning & Management, Clinical Research,- Medical/Scientific Support and Emerging Region Expansion**Job...

The Clinical Research Associate will oversee clinical trial activities to ensure ethical conduct, regulatory compliance, and high-quality data generation.Roles & Responsibilities:Assist in planning, initiation, execution, and closure of clinical trials.Conduct site monitoring visits (site selection, initiation, monitoring, close-out).Ensure adherence to...

Clinical Research Training, Clinical Research Assessments, Clinical Research Mock Tests, Clinical Research Overview, Clinical Research Mock Interviews, Clinical Trial Management **Job Types**: Full-time, Part-time, Contractual / Temporary, Freelance Expected hours: No less than 40 per week Schedule: - Day shift **Experience**: - total work: 5...