Job Opportunity: Clinical Research Associate (CRA) – Clinexel Life Sciences

Job Summary
Clinexel Life Sciences, a premier full-service Contract Research Organization (CRO), is seeking a dedicated and detail-oriented Clinical Research Associate (CRA) to join our team in Sanpada, Navi Mumbai. This role is ideal for experienced professionals who possess a strong foundation in clinical trial monitoring and a commitment to maintaining the highest standards of regulatory compliance. If you are passionate about advancing clinical research and thrive in a dynamic, professional environment, we invite you to contribute your expertise to our growing organization.

Job Overview

• Position: Clinical Research Associate (CRA)
• Location: Sanpada, Navi Mumbai, India
• Experience Required: 2 to 3 years of relevant clinical trial monitoring experience
• Education: Graduate or Postgraduate degree in Life Sciences or Pharmacy

Responsibilities

As a Clinical Research Associate, your primary focus will be to ensure the integrity of clinical trials through rigorous monitoring and proactive site management. Key responsibilities include:

• Site Monitoring: Conducting regular monitoring visits in strict accordance with approved study protocols to ensure patient safety and data reliability.
• Regulatory Compliance: Ensuring all trial activities align with Good Clinical Practice (GCP), ICH guidelines, and applicable local regulatory requirements.
• Performance Oversight: Monitoring site performance, tracking study progress, and addressing any deviations or delays promptly.
• Documentation and Reporting: Preparing accurate, detailed monthly and annual monitoring reports and maintaining comprehensive site visit records.
• Data Verification: Performing Source Data Verification (SDV) to confirm the accuracy and quality of trial data at the site level.
• Project Support: Assisting Project Managers with overall trial coordination and administrative tasks to ensure study milestones are met.
• Issue Resolution: Acting as the primary point of contact for sites to identify, investigate, and resolve operational or protocol-related issues as they arise.

Requirements

To be successful in this role, candidates must demonstrate the following qualifications and skill sets:

• Educational Background: A Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or a related field.
• Proven Experience: 2–3 years of hands-on experience in clinical trial monitoring within a CRO or pharmaceutical setting.
• Regulatory Knowledge: Deep understanding of GCP and ICH guidelines.
• Organizational Skills: Excellent time management skills with the ability to handle multiple clinical sites, manage competing priorities, and adhere to strict timelines.
• Communication: Exceptional verbal and written communication skills, with the ability to build professional relationships with site staff and internal stakeholders.
• Attention to Detail: Meticulous approach to data review and documentation.

Benefits

We believe in supporting the professional development and well-being of our team members. Joining Clinexel Life Sciences offers:

• Competitive Compensation: An expected salary range of ₹3.5 LPA to ₹6 LPA, commensurate with your experience and qualifications.
• Career Growth: Opportunities to build a long-term career with a reputable CRO that prioritizes skill development and professional advancement.
• Diverse Exposure: Hands-on experience working across a variety of clinical trials and complex regulatory processes.
• Collaborative Culture: A supportive and inclusive working environment that encourages teamwork and innovation.

How to Apply

If you meet the requirements and are eager to advance your career with Clinexel Life Sciences, please submit your updated CV for consideration.

Email your application to: [email protected]

Subject Line: Please ensure you include “CRA Application” in the subject line of your email to ensure your application is processed promptly.

Clinexel Life Sciences is an equal opportunity employer. We thank all applicants for their interest; however, only those selected for an interview will be contacted.