Cliantha Research, a globally recognized clinical research organization with offices in the USA, Canada, and India, is inviting passionate professionals to join its team at the Cliantha Corporate office in Ahmedabad. With a strong commitment to quality, innovation, and scientific excellence, Cliantha Research offers a dynamic work environment for those interested in advancing their careers in the clinical research field. The company is currently hiring for various roles, including Medical Writing, QA Auditing, and Laboratory Analysis.
Open Positions at Cliantha Research
- Sr. Officer/Executive – Medical Writing
- Experience: 2 to 5 years
- Qualification: B.Pharm / M.Pharm / M.Sc
- As a Medical Writing Officer or Executive, your role will involve creating and reviewing scientific and regulatory documents. You will collaborate with research teams to draft clinical study reports, protocols, and informed consent forms, ensuring accuracy and compliance with regulatory guidelines.
- QA Auditor – QA Clinic
- Experience: 2 to 5 years
- Qualification: B.Pharm / M.Pharm / M.Sc
- In this position, you will conduct audits in clinical settings, ensuring compliance with Good Clinical Practice (GCP) and regulatory standards. The QA Auditor will review clinical trials, identify areas for improvement, and ensure documentation and processes meet quality standards.
- Analyst – Large Molecule Lab
- Experience: 0 to 2 years
- Qualification: M.Sc Biotech
- As an Analyst in the Large Molecule Lab, you will be responsible for performing laboratory tests and analyzing large molecules such as proteins and nucleic acids. Your contributions will support bioanalysis for clinical studies, focusing on biotechnology and pharmaceutical products.
Responsibilities for Each Role
- Sr. Officer/Executive – Medical Writing:
- Prepare regulatory documents such as clinical study protocols and reports.
- Ensure accurate scientific communication aligned with industry standards.
- Collaborate with clinical and regulatory teams to meet deadlines.
- QA Auditor – QA Clinic:
- Perform internal and external audits to ensure GCP compliance.
- Review clinical data and documentation to detect inconsistencies.
- Provide feedback to clinical teams for maintaining quality assurance.
- Analyst – Large Molecule Lab:
- Conduct bioanalytical tests for large molecules, including proteins and nucleic acids.
- Record data, perform statistical analyses, and ensure the validity of results.
- Maintain laboratory equipment and ensure compliance with safety protocols.
Qualifications and Skills Required
- Medical Writing: Strong understanding of clinical research, excellent writing skills, and familiarity with regulatory guidelines.
- QA Auditor: Knowledge of GCP standards, attention to detail, and experience in quality auditing in a clinical setting.
- Analyst (Biotech): A solid background in biotechnology, strong analytical skills, and experience in a laboratory environment.
How to Apply
If you are passionate about making a difference in the field of clinical research and meet the qualifications for any of these positions, Cliantha Research welcomes your application. Interested candidates can send their resumes to:
- Email: recruitment1@cliantha.com, srchauhan1@cliantha.com
- Company Website: Cliantha.com
