Clinical Research associate-Reputed Medical

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...

Company DescriptionAdmerus Biosciences, headquartered in Hyderabad, India, is a Contract Research Organization (CRO) that services the global Biopharma industry. We partner with reputed global biopharma and research laboratories to find efficient, cost-effective, and innovative solutions to their clinical development challenges. Our focus is on delivering...

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....

**Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures. A Clinical Research Associate, also known as a CRA, conducts research to ensure these products are safe.** **Salary**: ₹500,000.00 - ₹600,000.00 per year **Benefits**: - Health insurance Schedule: - Day...

Novartis is a pioneer in drug development with a robust pipeline across therapy areas. CRMAs work closely with Investigators and ensure scientific engagement with the Investigator community to drive our programs and trials across the globe. Your responsibilities include, but are not limited to: - Closely collaborates with the Trial Monitoring Organisation...

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...

Develop and outline the purpose and methodology of trials - Present trial protocols to a leading committee - Identify and assess the suitability of facilities to be used at a clinical trial site - Document site visits, issue reports, and follow-up letters to a site - Visit trial sites on regular basis to conduct clinical trials on new drugs or medical...

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...

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (i CRO). We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally...

Job Description Job Title: Clinical Research AssociateBusiness Unit: Clinical ResearchLocation: Hyderabad At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.Are You Ready to Create Your Own Sunshine? As you enter...