CliantHa Research Hiring Clinical Data Analyst & Medical Writer | Ahmedabad

CliantHa Research, a leading Clinical Research Organization (CRO), is seeking talented and experienced professionals to join our growing team in Ahmedabad. We have immediate openings for a Clinical Data Analyst and a Medical Writer. If you are passionate about clinical research and are looking for a challenging and rewarding career, we encourage you to apply.

Career Opportunities at CliantHa Research in Ahmedabad

At CliantHa Research, we are committed to providing high-quality clinical research services to our clients. We offer a dynamic and collaborative work environment where you can contribute to महत्वपूर्ण clinical trials and make a real difference in the healthcare industry. Join our team in Ahmedabad and take the next step in your clinical research career.

About CliantHa Research

CliantHa Research is a global CRO with a strong presence in the USA, Canada, and India. We provide a full spectrum of clinical research services, from early-phase studies to post-marketing surveillance. Our commitment to quality, innovation, and patient safety makes us a trusted partner for pharmaceutical and biotechnology companies worldwide.

Job Openings

Clinical Data Analyst

We are looking for a detail-oriented Clinical Data Analyst to manage and analyze clinical trial data. Your responsibilities will include data cleaning, database management, and generating reports. You will work closely with the clinical operations and biostatistics teams to ensure the integrity and accuracy of clinical trial data.

**Qualification:** B.Pharm, M.Pharm, Pharm.D

**Experience:** 2 to 4 years in CDM (Clinical Data Management)

Medical Writer

We are seeking a skilled Medical Writer to develop high-quality clinical and regulatory documents. Your responsibilities will include writing clinical study reports, protocols, investigator brochures, and other medical communication materials. You will work collaboratively with medical experts and clinical teams to ensure the accuracy and clarity of scientific information.

**Qualification:** M.Pharm, Pharm.D

**Experience:** 3 to 6 years in Clinical Trials

Qualifications and Experience

For **Clinical Data Analyst:** Bachelor’s or Master’s degree in Pharmacy (B.Pharm/M.Pharm/Pharm.D) or a related scientific field with 2 to 4 years of experience in Clinical Data Management (CDM).
For **Medical Writer:** Master’s or Doctorate degree in Pharmacy (M.Pharm/Pharm.D) or a related scientific field with 3 to 6 years of experience in writing clinical trial documents.
Strong understanding of clinical research processes and regulatory guidelines.
Excellent written and verbal communication skills.
Proficiency in relevant software and tools.
Ability to work independently and as part of a team.