Cliantha Research Hiring for Business Development & Medical Writer Roles
Cliantha Research Hiring for Business Development & Medical Writer Roles | Join Us in Ahmedabad
Cliantha Research, a leading global provider of clinical research services, is looking for passionate professionals to join our team at our Ahmedabad location. We offer exciting opportunities in Business Development and Medical Writing for individuals eager to make a meaningful impact in healthcare research.
Job Openings Overview
- Company: Cliantha Research
- Location: Ahmedabad, India
- Available Positions: Business Development, Medical Writer
- Experience Required: 1 to 10 years (depending on the role)
- Qualification: B Pharmacy, M Pharmacy, Pharm D, MBA (Marketing), MSc
- Global Presence: USA, Canada, India
1. Business Development Executive/Manager
Location: Ahmedabad
Qualification: B Pharmacy, M Pharmacy, Pharm D, MSc, or MBA (Marketing)
Experience: 5 to 10 years in business development within the pharmaceutical or clinical research sectors
Key Responsibilities:
- Identify and develop new business opportunities in the clinical research industry
- Build and maintain strong client relationships
- Coordinate with cross-functional teams to ensure client satisfaction and project delivery
- Prepare and deliver presentations and proposals to potential clients
- Negotiate and close deals to meet sales targets
Skills Required:
- In-depth knowledge of the clinical research industry and regulatory landscape
- Excellent communication and negotiation skills
- Proven ability to manage multiple clients and projects simultaneously
- Proactive, independent work style
- Strong problem-solving and analytical skills
2. Medical Writer
Location: Ahmedabad
Qualification: B Pharmacy, M Pharmacy, or Pharm D
Experience: 1 to 4 years in medical writing or related fields
Key Responsibilities:
- Write clinical study protocols, informed consent forms, study reports, and regulatory submission documents
- Collaborate with clinical teams and subject matter experts to ensure accurate and clear documentation
- Ensure compliance with regulatory and ethical guidelines
- Stay updated with current medical research and industry standards
Skills Required:
- Excellent written and verbal communication skills
- Strong understanding of medical terminology, clinical research processes, and regulatory requirements
- Attention to detail and ability to meet deadlines
- Familiarity with ICH and GCP regulatory standards is a plus
- Ability to simplify complex scientific data for diverse audiences
How to Apply:
Email Your Resume To: