KV Clinical Research Pvt Ltd, a Site Management Organization (SMO), has announced openings for the position of Clinical Research Coordinator (CRC). The vacancies are available in Ranchi and Deoghar for candidates with at least 1 year of clinical research experience.
Candidates with B.Pharm, M.Pharm, Pharm.D, Diploma in Clinical Research, or M.Sc in Clinical Research qualifications can apply for these Clinical Research Coordinator jobs.
This opportunity may suit clinical research professionals looking to build experience in clinical trial coordination and site-level research activities.
Job Details
| Particular | Details |
|---|---|
| Company | KV Clinical Research Pvt Ltd |
| Position | Clinical Research Coordinator (CRC) |
| Industry | Clinical Research |
| Organization Type | Site Management Organization (SMO) |
| Qualification | B.Pharm, M.Pharm, Pharm.D, Diploma in Clinical Research, M.Sc in Clinical Research |
| Experience | 1+ Year in Clinical Research |
| Location | Ranchi & Deoghar |
| Employment Type | Full-Time |
| Application | Email CV |
Responsibilities
While the vacancy notice does not provide a detailed responsibility list, a Clinical Research Coordinator typically supports site-level clinical trial activities such as:
- Coordinating day-to-day clinical research activities at the study site.
- Supporting investigators in conducting clinical studies according to the approved protocol.
- Maintaining clinical trial documentation and essential study records.
- Coordinating participant visits and study-related procedures.
- Supporting informed consent and participant documentation processes as applicable.
- Assisting with CRF/eCRF documentation and data coordination.
- Coordinating with investigators, sponsors, CROs and other clinical research stakeholders.
- Supporting compliance with applicable study protocols, SOPs and Good Clinical Practice requirements.
Note: The responsibilities above describe typical CRC activities and should not be interpreted as additional requirements stated by KV Clinical Research.
Qualification & Eligibility
Candidates with the following qualifications are mentioned in the vacancy:
- B.Pharm
- M.Pharm
- Pharm.D
- Diploma in Clinical Research
- M.Sc in Clinical Research
Applicants should have at least 1 year of experience in clinical research.
Candidates with previous exposure to clinical trial sites, site coordination, clinical trial documentation, GCP processes or study coordination may find their experience relevant to this CRC vacancy.
Why Consider This Opportunity?
A Clinical Research Coordinator position can provide valuable site-level exposure to clinical trials and interactions with investigators and other clinical research stakeholders.
The role can help professionals strengthen practical knowledge of clinical trial coordination, study documentation, participant management and regulatory compliance while building a long-term career in the clinical research industry.
How to Apply
Interested and eligible candidates can prepare an updated CV highlighting their clinical research experience, qualification and relevant clinical trial skills.
Send CV to: hr@kvclinicalresearch.com
