Cliantha Research is hiring for Medical Monitor, Medical Writer, and Proposal Developer positions in Ahmedabad. This is a great pharma jobs opportunity for MBBS, MD Pharmacology, M.Pharm, and Pharm.D professionals in clinical research and medical writing. Apply now for these pharmaceutical careers in India.
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About the Company
Cliantha Research is a full-service Contract Research Organization (CRO) with a strong presence in India, USA, and Canada. The company specializes in clinical research, clinical trials, and related pharmaceutical services.
Known for its high quality standards, regulatory compliance, and innovative approach, Cliantha supports global pharmaceutical and biotech companies in bringing new therapies to market efficiently. With operations across multiple countries, it offers excellent exposure and growth opportunities in the clinical research sector.
Job Details
- Company Name: Cliantha Research
- Experience: Varies by role (0–4 years)
- Qualification: MBBS, MD Pharmacology, M.Pharm (Pharmacology), Pharm.D, B.Pharm
- Location: Ahmedabad
- Work Type: On-site
Job Description
Cliantha Research is expanding its clinical research team and inviting talented professionals for key roles in medical monitoring, medical writing, and proposal development. These positions play a vital role in supporting clinical trials and regulatory documentation. The openings are ideal for candidates seeking dynamic careers in the clinical research and pharmaceutical industry.
Medical Monitor
- Department: Medical Monitoring / Clinical Research
- Role: Medical Monitor
- Experience: 0 to 2 years (Freshers can apply)
- Education/Qualification: MBBS or MD Pharmacology
Medical Writer
- Department: Medical Writing
- Role: Medical Writer
- Experience: 3 to 4 years
- Education/Qualification: M.Pharm (Pharmacology) / Pharm.D
Proposal Developer
- Department: Business Development / Proposals
- Role: Proposal Developer
- Experience: 2 to 3 years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Strong medical and pharmacological knowledge
- Excellent scientific writing and communication skills
- Understanding of clinical trial processes and regulations
- Experience in medical writing or clinical monitoring
- Ability to work in a fast-paced environment
- Good documentation and proposal development skills
Key Responsibilities
- Monitor clinical trial safety and progress
- Prepare high-quality medical and regulatory documents
- Develop clinical trial proposals and budgets
- Review clinical data and ensure compliance
- Coordinate with cross-functional teams
- Support regulatory submissions and queries
Benefits/Perks
- Competitive salary and growth opportunities
- Global exposure in clinical research
- Learning in international regulatory standards
- Collaborative and innovative work culture
- Professional development in clinical domain
How to Apply
Interested candidates should send their updated resume to mjunnarkar@cliantha.com. For more pharma jobs and clinical research opportunities in India, visit Pharma Recruiter. Apply now and advance your career with Cliantha Research!
Why You Should Join
Cliantha Research offers a vibrant and growth-oriented environment for professionals in clinical research. With operations in India, USA, and Canada, the company provides global exposure and excellent learning opportunities. Employees enjoy a supportive culture focused on innovation, quality, and long-term career development in the pharmaceutical and clinical research industry.
FAQs
Q1: What positions are open at Cliantha Research Ahmedabad?
A: Medical Monitor, Medical Writer, and Proposal Developer.
Q2: Are freshers eligible for any role?
A: Yes, freshers with MBBS or MD Pharmacology can apply for Medical Monitor position.
Q3: What is the job location?
A: Ahmedabad, Gujarat.
Q4: How do I apply for these pharma jobs?
A: Email your resume to mjunnarkar@cliantha.com.
