Cliantha Research Clinical Vacancies: Medical Writing, QA Auditor, Large Molecule Lab | Biotech Freshers Welcome

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.

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