Clinical Research professional

Company Description

Vyas Cancer Research (VCR Park) is a collaborative facility located in Andhra Pradesh, India. It fosters partnerships between service partners, entrepreneurs, ideators, and professionals to translate ideas into products or services. VCR Park provides state-of-the-art labs (for lease and service), office space, and common areas, creating a vibrant translational oncology ecosystem.

Role Description

Dedicated Clinical Research professional with a degree in MPharma or Pharma D, seeking to excel as a Clinical Research Coordinator in Hyderabad or Bengaluru, with expertise in site management, subject screening and enrollment, adverse event reporting, source document verification, and maintaining meticulous study records. Experienced in conducting research, performing data collection and analysis, supporting laboratory activities, and contributing to project planning and execution, along with preparing reports, assisting with regulatory documentation, and collaborating with interdisciplinary teams to advance oncology research and ensure the successful, ethical execution of clinical trials.

Qualifications

• Master's degree in Pharmacy (MPharma) or Doctor of Pharmacy (Pharm D) from a recognized institution
• Strong understanding of clinical research processes, including ICH-GCP guidelines and regulatory requirements
• Hands-on experience or training in site management, subject recruitment, and clinical trial coordination
• Knowledge of adverse event reporting, source document verification, and case report form (CRF) completion
• Proficiency in data collection, analysis, and maintaining accurate study documentation
• Familiarity with laboratory procedures and oncology research methodologies is an advantage
• Ability to prepare technical reports, regulatory documents, and study-related documentation
• Strong organizational, analytical, and problem-solving skills
• Excellent communication and interpersonal skills for effective collaboration with multidisciplinary teams
• Proficiency in MS Office and clinical data management systems
• High attention to detail with a commitment to ethical standards and patient safety
• Familiarity with oncology research and/or experience in clinical research is a plus