Senior Clinical Research Coordinator

3 days ago

Pune, Maharashtra, India beBeeClinicalResearch Full time ₹ 8,00,000 - ₹ 12,00,000

We are seeking a diligent Clinical Research Associate to join our team. A Clinical Research Associate plays a crucial role in the success of clinical trials by ensuring that research sites adhere to Good Clinical Practice (GCP) guidelines and regulatory requirements.

Key Responsibilities:
  • Writing Drug Trial Methodologies: Assist in developing, implementing, and maintaining drug trial methodologies and procedural documentation. This includes writing clear, concise protocols, case report forms, and informed consent documents.
  • Identification and Briefing of Trial Investigators: Support the identification and briefing of appropriate trial investigators (clinicians). This involves communicating effectively with clinicians to ensure they understand the trial objectives, methods, and expected outcomes.
  • Clinical Site Management: Coordinate with clinical sites and ensure effective communication with trial centre staff. This includes conducting site visits, providing training and support, and addressing any questions or concerns.
  • Trial Materials Design: Help design trial materials and ensure study centres receive sufficient quantities of all required documents and supplies. This includes managing inventory, coordinating logistics, and troubleshooting issues as needed.
  • Collaboration and Communication: Collaborate closely with internal teams and investigators to ensure smooth trial execution. This involves working effectively with cross-functional teams, communicating clearly, and resolving conflicts promptly.
  • Trial Records and Compliance: Maintain updated trial records and assist in compliance with regulatory requirements. This includes tracking data, reporting adverse events, and ensuring adherence to GCP guidelines.
Requirements:
  • Bachelor's degree in a relevant field (e.g., life sciences, healthcare).
  • Minimum 1-2 years of experience in clinical research or a related field.
  • Excellent communication, organizational, and problem-solving skills.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Familiarity with Good Clinical Practice (GCP) guidelines and regulatory requirements.
Benefits:
  • Opportunity to work on cutting-edge clinical trials.
  • Collaborative and dynamic work environment.
  • Professional development opportunities.
  • Competitive compensation package.
Why Join Us:

At [Company Name], we value our employees' contributions and offer a range of benefits to support their well-being and career growth. We are committed to creating a positive and inclusive work environment where everyone can thrive.

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