Cliantha Research Hiring in CDM, SAS, Medical Writer, Clinical Trials, Buisness development

Cliantha Research, a globally recognized Contract Research Organization (CRO), specializes in clinical trials, consumer research, and late-phase research. With a presence in the USA, Canada, and India, the company is committed to delivering high-quality clinical research services to healthcare and pharmaceutical industries. Their team thrives on innovation and collaboration, ensuring precision and compliance in all projects. If you’re looking for a challenging and rewarding career, Cliantha Research has multiple openings in its Clinical Trials department in Ahmedabad.

Explore Our Exciting Job Opportunities

1. Business Development

• Responsibilities:
  Develop and execute strategic plans to expand client base and revenue streams. Foster long-term relationships with clients, identify market trends, and prepare detailed reports on business performance.
• Qualifications:
  A Bachelor’s or Master’s degree in Pharmacy (B. Pharm, M. Pharm, Pharm.D), or Science (M.Sc), with an MBA in Marketing preferred.
• Experience Required:
  8-10 years in Business Development roles within the clinical research or pharmaceutical industry.
• Key Skills:
  Strong negotiation skills, market analysis, client relationship management, and strategic planning.

2. Late Phase Contracts & Proposal Developer

• Responsibilities:
  Develop and manage contracts and proposals for late-phase clinical trials. Collaborate with project teams and clients to ensure contracts align with project goals.
• Qualifications:
  A Bachelor’s or Master’s degree in Pharmacy (B. Pharm, M. Pharm) or Science (M.Sc).
• Experience Required:
  3-4 years in contract and proposal development.
• Key Skills:
  Attention to detail, strong communication, and contract negotiation skills.

3. Medical Writer – Consumer Research

• Responsibilities:
  Prepare scientific documents, including protocols, reports, and consumer research materials. Ensure accuracy, clarity, and compliance with regulatory standards.
• Qualifications:
  A degree in Pharmacy (B. Pharm, M. Pharm) or Pharm.D.
• Experience Required:
  3-6 years in medical writing.
• Key Skills:
  Excellent written communication, regulatory knowledge, and scientific accuracy.

4. SAS Programmer

• Responsibilities:
  Perform data analysis using SAS programming for clinical trials. Create datasets, generate reports, and ensure data integrity.
• Qualifications:
  A degree in Pharmacy (B. Pharm, M. Pharm) with SAS Certification.
• Experience Required:
  3-4 years in SAS programming within clinical data management.
• Key Skills:
  Proficiency in SAS, statistical analysis, and attention to detail.

5. Clinical Data Analyst (CDA I)

• Responsibilities:
  Manage clinical trial data, including data collection, validation, and reporting. Ensure adherence to CDM processes and regulatory standards.
• Qualifications:
  A degree in Pharmacy (B. Pharm, M. Pharm, Pharm.D).
• Experience Required:
  2-4 years in Clinical Data Management (CDM).
• Key Skills:
  Analytical thinking, knowledge of clinical data systems, and regulatory compliance.

How to Apply

If you’re ready to embark on an exciting career with Cliantha Research, follow these steps to apply:

1. Prepare an updated resume highlighting your qualifications, experience, and relevant skills.
2. Send your resume to mjunnarkar@cliantha.com or vdesai@cliantha.com.