Clinical Research Professional

Company Description

Since its establishment in 2007, Auriga Research Private Limited (ARL) has become a leading Contract Research Organization (CRO), offering a comprehensive range of services. We specialize in Clinical Trials, Pharmacovigilance, Clinical Data Management, and Cosmetic Studies, supporting the pharmaceutical, biological, herbal, cosmetic, nutraceutical, and medical device industries. Our expertise helps clients secure timely approvals while complying with national and international guidelines. Utilizing advanced Clinical Trial Management Systems and robust data management, we ensure high-quality, regulatory-compliant clinical trials and studies.

Role Description

This is a full-time on-site role for a Clinical Research Professional based in Manesar. The Clinical Research Professional will be responsible for managing clinical trials, including Site Initiation Visits (SIV), site monitoring, and site closeouts. They will ensure compliance with Good Clinical Practice (GCP) and manage the collection, analysis, and reporting of clinical data. The role also involves conducting bioequivalence studies, pharmacokinetic analyses, and ensuring the safety and efficacy of cosmetic studies through rigorous quality management systems.

Qualifications

• Strong Analytical Skills and Statistical knowledge
• Experience in Market Research and general Research methodologies
• Proficient Laboratory Skills
• Excellent written and verbal communication skills
• Ability to work independently and collaborate with a team
• Experience in the clinical research, pharmaceutical, or related industries is a plus
• Bachelor's or Master's degree in Life Sciences, Pharmacy, Chemistry, or related field