Job Opportunity: Ethics Committee Coordinator cum Clinical Research Associate (CRA)

Job Summary

We are currently seeking a motivated and detail-oriented Pharm D graduate to join our team in Hyderabad as an Ethics Committee Coordinator cum Clinical Research Associate (CRA). This is an urgent, entry-level position designed for freshers looking to build a robust professional foundation in the clinical research industry. You will receive hands-on exposure to clinical trial lifecycles, regulatory compliance, and ethics committee operations. This role is an ideal stepping stone for those pursuing long-term career growth in clinical research, pharmacovigilance, and regulatory affairs.

Responsibilities

As an Ethics Committee Coordinator cum CRA, you will play a vital role in ensuring that clinical trials are conducted in strict accordance with ethical standards and regulatory requirements. Your daily responsibilities will include:

• Ethics Committee Coordination: Managing the preparation, submission, and tracking of applications to Ethics Committees to ensure timely trial approvals and documentation.
• Clinical Trial Monitoring: Assisting in on-site clinical trial monitoring activities under the guidance of senior team members.
• Regulatory Compliance: Maintaining essential documents, regulatory files, and compliance records, ensuring all trial activities adhere to ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines.
• Communication: Acting as a point of contact for investigators, clinical trial sponsors, and site teams to facilitate smooth, efficient trial execution.
• Documentation: Ensuring high standards of accuracy in reporting and record-keeping throughout the lifecycle of the trial.

Requirements

We are looking for a dedicated professional who is ready to jump-start their career in a fast-paced environment. To be eligible for this role, you must meet the following criteria:

• Educational Qualification: A Pharm D degree is mandatory.
• Experience: This is an exclusive opportunity for freshers.
• Gender: Male candidates only.
• Technical Knowledge: A solid conceptual understanding of the clinical research process, ICH-GCP guidelines, and the regulatory framework governing clinical trials.
• Skills: Exceptional communication and organizational skills, with an ability to coordinate effectively between multiple stakeholders.
• Teamwork: A proactive approach to working within a team-oriented clinical environment.
• Availability: Ability to join the team immediately.

Benefits

Joining our team offers more than just a job; it provides a comprehensive learning experience that will define your career trajectory. Benefits include:

• Competitive Starting Compensation: An annual CTC of ₹2,50,000.
• Professional Development: Real-world experience in ethics committee operations, which is a highly sought-after skill set in the industry.
• Career Foundation: A clear pathway to future roles in Clinical Research Associate (CRA), Clinical Trial Assistant (CTA), Pharmacovigilance, and Regulatory Affairs.
• Industry Exposure: Direct involvement in clinical trial lifecycles, providing you with the technical expertise required to transition into top-tier Clinical Research Organizations (CROs).

How to Apply

If you are a Pharm D graduate with a passion for clinical research and meet the specified requirements, we encourage you to apply immediately.

Please send your updated resume to:
Email: [email protected]

Subject Line: Please use the subject line: “Application for CRA – Pharm D Fresher” to ensure your application is processed promptly.