Leading Clinical Research Organization (CRO) Insignia Clinical Services Pvt. Ltd. is dedicated to improving healthcare via the execution of superior clinical studies. Insignia, a pharmaceutical company with a reputation for excellence that partners with world-class companies to bring cutting-edge treatments to market, is based in the center of Delhi. Insignia provides the ideal environment for professional advancement if you have a strong interest in clinical research and want to have a significant influence in the healthcare industry.

Responsibilities as a Clinical Research Associate

You will be essential to the accomplishment of our clinical studies as a Clinical Research Associate (CRA) at Insignia Clinical Services. Your main duties will be as follows:

• Supervising clinical trial sites to guarantee adherence to the study protocol, Good Clinical Practice (GCP), and regulatory mandates is known as monitoring clinical trials.
• Data collection and verification: Examining source documents and case report forms (CRFs) to guarantee the completeness and correctness of clinical data.
• Site Coordination: Handling any problems or inquiries that may come up as the primary point of contact between the clinical trial locations and the research sponsor.
• Reporting: To guarantee that the study proceeds smoothly, comprehensive reports on the trials’ progress, including any deviations or unfavorable events, should be prepared.

Qualifications Required

In order to be given consideration for the position of Clinical Research Associate at Insignia, applicants must fulfill the following requirements:

• Educational Background: A postgraduate university degree or its equivalent is required, ideally in the biological sciences or a related field to healthcare.
• Experience in the Pharmaceutical sector: A minimum of one year working as a Clinical Research Associate for a CRO or the pharmaceutical sector.
• Compliance Knowledge: This position requires a thorough understanding of GCP rules and regulatory regulations.

Skills and Attributes

A combination of hard and soft abilities is needed to succeed in the position of Clinical Research Associate, including:

• Pay Close Attention to Detail: Accurate monitoring of trials and data verification are essential for guaranteeing the authenticity and dependability of the results of clinical studies.
• Strong Communication: To effectively communicate with trial sites, sponsors, and regulatory agencies, one must possess excellent verbal and written communication skills.
• Ability to Solve Problems: The capacity to recognize, analyze, and come up with solutions for problems that might come up during a clinical trial.
• Organizational abilities: Ability to manage several trial sites and guarantee timely reporting through effective time management and organizational abilities.

How to Apply

Applying for this fantastic opportunity at Insignia Clinical Services Pvt. Ltd. is highly encouraged if you have a strong interest in clinical research and fulfill the necessary requirements. How to apply is as follows:

Send Your CV by Email: With “Application for Clinical Research Associate-Delhi” in the subject line, send your most recent CV to careers@insigniacs.com.