Contract & Proposal Specialist
Ahmedabad, Gujarat, India · Full Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 10 ਘੰਟੇ ਪਹਿਲਾਂ
- Work mode
- In office
- Education
- B.Pharm/M.Sc.
- Eligibility
- Candidates with B.Pharm or M.Sc. qualifications can apply; law graduates are excluded from consideration.
- Resume
- Required to apply
Where you'll work
Job description
About Cliantha Research Limited
Cliantha Research Limited operates as a comprehensive clinical research organization, providing complete solutions across all phases of clinical trials, along with consumer clinical research, bioanalytical services, biometrics, medical services, allergy testing, and veterinary therapeutics. With over 21 years of expertise and advanced clinical and bioanalytical facilities in India and North America, the company delivers ethical and scientifically sound services to pharmaceutical, biotech, and healthcare sectors. Cliantha employs more than 1,500 professionals and maintains compliance and excellence through rigorous inspections by global regulatory bodies.
Role Overview
We seek an on-site Contract & Proposal professional for our Ahmedabad office. This full-time role involves crafting, scrutinizing, and managing contracts and proposals related to clinical research projects to ensure accuracy, consistency, and adherence to company and regulatory standards. You will coordinate with multiple departments to collect project-specific information, prepare cost analyses and proposals, and negotiate contract terms with sponsors and partners under senior guidance. Additionally, you'll be responsible for maintaining a central contract repository, monitoring contract progress and key dates, facilitating prompt contract execution including amendments, analyzing contractual risks, proposing risk mitigation plans, and helping enhance templates and workflow processes.
Candidate Profile and Qualifications
- Applicants with degrees in B.Pharm or M.Sc. are eligible; legal or law graduates should not apply.
- Strong expertise in contract management, including drafting, reviewing, and maintaining clinical research agreements and related documentation is essential.
- Proficiency in contract negotiation and clear communication to coordinate with sponsors, vendors, and internal teams is required to ensure favorable and compliant contract terms.
- Prior relevant experience handling contracts and proposals within a clinical research organization environment is necessary.
Additional Information
Interested candidates are invited to submit their resumes via email to [email protected].