Clinical Research Coordinator

Company DescriptionConcept Clinical Service is a Research Management Organization dedicated to supporting clinical trials in the pharmaceutical, biotechnology, and medical device industries. Our services ensure stringent adherence to protocols, extensive documentation, quality data collection and reporting, and compliance with ICH-GCP and other regulatory...

Msc life sciences - B.Pharm/M. Pharm/ Pharm. D - Freshers or Experienced - Willing to build a career in the filed of Clinical Research with good exposure and new development in terms of technologies and treatment. - Working place will be the multispecialtiy hospital in surat - Good communication skill with basic computer skill. - should be a good learner...

candidate of Life science GraduateMsc life sciencesB.Pharm/M. Pharm/ Pharm. DFreshers or ExperiencedWilling to build a career in the filed of Clinical Research with good exposure and new development in terms of technologies and treatment.Working place will be the multispecialtiy hospital in suratGood communication skill with basic computer skill.should be a...

**Job Summary**: We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to manage and coordinate clinical trials, ensuring compliance with regulatory guidelines and protocols. The CRC will work closely with principal investigators, study participants, and regulatory bodies to support successful trial execution. **Key...

**Responsibilities** - Develop and maintain study protocols and case report forms. - Recruit and screen study participants per study criteria. - Obtain informed consent from study participants and explain study procedures. - Collect and manage study data, including adverse events and other safety-related information. - Monitor study participant compliance...

Bsc/Msc life science/paramedical - B.Pharm/M. Pharm/ Pharm. D - Freshers or Experienced - Willing to build a career in the filed of research with good exposure and new development in terms of technologies and treatment. - Working place will be the hospital. - Good communication skill with basic computer skill. - should be a good learner with adaptable, Soft...

Job Responsibility: ❖ Lead and manage the day-to-day conduct of clinical trials at the site. ❖ Ensure adherence to study protocols, ICH-GCP guidelines, and regulatory requirements. ❖ Serve as the primary point of contact between the site and the sponsor/CRO. ❖ Prepare, submit, and maintain regulatory documents (e.g., EC/IRB submissions, clinical...

**Job description for the QA profile: -** **Company: Clinvigilant Research Pvt. Ltd** **Location: Ahmedabad(On-Site)** **Position: 01 (One)** **Experience: 03 + Years.** **Job description: - ** - **Ensuring compliance**: Ensuring that clinical processes are conducted in accordance with regulations and guidelines - **Managing quality assurance...

(Job code: CBCCIND/CO/CRA) Work Experience: 4-8 Years Work Location: Ahmedabad, Mumbai, Bangalore, Hyderabad, Pune or Delhi Pre-Requisite Skills: onsite monitoring experience mandatory Job Requirements: - Key Responsibilities - Overall site management of clinical trials - Ensure effective communication to sites - Prepare for site visits - Assist PM in...

Typical employers of pharmacologists - Pharmaceutical companies - Universities - The NHS - The Medical Research Council - Other government research organisations. The recruitment process may involve a technical interview. Qualifications and training required There are routes into pharmacology for graduates and school leavers. Graduates need a degree in a...