Cliantha Research, a global leader in clinical trials and research services, is currently hiring for several key positions at its
Ahmedabad Corporate Office. Whether you're an experienced professional or a fresh graduate in
Biotechnology,
Pharmacy, or related fields, Cliantha Research offers a chance to grow in a dynamic work environment. Explore the vacancies and see if your qualifications match the roles in
Medical Writing,
Quality Assurance (QA) Auditing, or the
Large Molecule Lab.
1. Medical Writing Officer/Executive
Location: Cliantha Corporate, Ahmedabad
Experience: 2 to 5 years
Qualification: B.Pharm, M.Pharm, or M.Sc
In the role of
Medical Writing Officer/Executive, you will be responsible for creating high-quality clinical documents, including study protocols, reports, and regulatory submissions. The ideal candidate should have a strong understanding of clinical research protocols and the ability to present complex scientific data in a clear and concise manner.
Key Responsibilities:
- Write and review clinical study reports, protocols, and regulatory submissions.
- Collaborate with cross-functional teams, including clinical operations and regulatory affairs.
- Ensure that all documentation is compliant with regulatory standards.
This position offers a fantastic opportunity to hone your
medical writing skills and gain exposure to global regulatory frameworks. If you have the right qualifications and experience, this could be your chance to advance in the growing field of medical writing.
2. QA Auditor - QA Clinic
Location: Cliantha Corporate, Ahmedabad
Experience: 2 to 5 years
Qualification: B.Pharm, M.Pharm, or M.Sc
The
QA Auditor position focuses on maintaining and improving the
Quality Assurance processes in the clinic. You will conduct regular audits to ensure that the clinical trial procedures meet all compliance and quality standards.
Key Responsibilities:
- Perform internal audits of clinical trial processes.
- Ensure compliance with Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) guidelines.
- Identify areas for improvement and assist in implementing corrective actions.
This role is ideal for candidates with a background in
Quality Assurance who are looking to contribute to the integrity and quality of clinical trials at Cliantha Research.
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Cliantha Research - A Top full-service Global Clinical Research Organization (CRO) in Gujarat, India Recruitment - Job vacancies[/caption]
3. Analyst - Large Molecule Lab (Biotech Freshers Welcome)
Location: Cliantha Corporate, Ahmedabad
Experience: 0 to 2 years
Qualification: M.Sc in Biotechnology
Are you a
Biotech Fresher eager to start your career in clinical research? The position of
Analyst in the Large Molecule Lab could be the perfect entry point for you. In this role, you will support large molecule analysis by conducting experiments, analyzing data, and ensuring lab compliance with all relevant regulations.
Key Responsibilities:
- Perform bioanalytical tests on large molecules.
- Work closely with senior analysts to prepare reports on lab findings.
- Ensure that all experiments are carried out according to Standard Operating Procedures (SOPs).
This is an excellent opportunity for fresh
M.Sc Biotechnology graduates to gain hands-on experience in a cutting-edge lab environment.
How to Apply
Interested candidates are encouraged to send their resumes to:
Email: recruitment1@cliantha.com,
srchauhan1@cliantha.com
https://pharmastuff.org.in/job/cliantha-research-clinical-vacancies
