Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
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Cliantha Research is headquartered in India with facilities in Ahmedabad, Noida, and Vadodara. Cliantha has a presence in the USA (facilities in Florida and Project Management in New Jersey), Canada (facilities in Mississauga, Winnipeg, and Scarborough), and Portugal (Project management).
In fifteen years, Cliantha has accumulated expertise in Early Phase (BA/BE), First in Man, Late Phase (various therapeutic areas), Respiratory, Tobacco Research, Dermatology, Consumer Research, Analytical lab, Diagnostic Central lab, IVRT, IVPT, Biometrics, Environmental Exposure Chambers and Medical Services.
Position: Project Manager – Clinical Trials
Location: Ahmedabad, Gujarat, India
Job Description:
- Coordination and supervise the study team for the study feasibility and PI (Principal
Investigator) database updates. - Coordination with the sponsors to drive the project deliverable and timelines.
- Â Review of study documents and Co-monitoring/other clinical research-related activities.
- Create and implement Project Management Plan, Operational Planning, Analysis, Risk
Assessment and Resolution Strategies. - Project finance tracking & Milestone tracking.
- Responsible for monitoring the progress/performance of all projects to include quality of
services provided timeliness of deliverable, compliance with regulatory requirements, and adherence to financial targets. - Manage and direct the efforts of CRA/CTA.
- Ensure to follow and adhere to policies and applicable SOP and provide feedback on SOP, procedures, and practices for better development for future projects.
Desired Candidate Profile:
- Excellent organizational, leadership, and problem-solving skills.
- Excellent written and verbal communication skills.
- Experience in leading cross-functional teams to meet goals and metrics.
- Know-how in managing Phase clinical studies.
- Thorough knowledge of GCP, ICH guidelines, and regulatory requirements for clinical trial management.
Qualification: BAMS/BHMS, B.Pharma/B.Sc, MS/M.Sc, M.Pharma
Experience: 10-14 Years
Salary: Negotiable
Contact Details:
dmirchandani@cliantha.com, careers@cliantha.com, hr@cliantha.com
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