Clinical Research Coordinator

Job Title: Clinical Research Associate (CRA) - Oncology

Job Type: Full-time

About Us: Our client is a leading organization dedicated to advancing medical research and improving patient outcomes. Their focus is on developing innovative treatments and therapies, with a strong emphasis on oncology. We are committed to conducting high-quality clinical trials and ensuring the highest standards of scientific integrity.

Job Summary: Currently assisting my client to identify and hire a highly motivated and detail-oriented Clinical Research Associate (CRA) to join the oncology research team. The CRA will be responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements, study protocols, and Good Clinical Practice (GCP) guidelines. The ideal candidate will have a strong background in oncology, excellent organizational skills, and a passion for contributing to cutting-edge cancer research.

Key Responsibilities:

• Monitor clinical trials at investigative sites to ensure adherence to study protocols, GCP, and regulatory requirements.
• Conduct site initiation, routine monitoring, and close-out visits.
• Review and verify case report forms (CRFs) and source documents for accuracy and completeness.
• Ensure timely and accurate data collection, entry, and reporting.
• Communicate effectively with investigators, site staff, and the clinical research team to address and resolve issues.
• Assist in the preparation and submission of regulatory documents and ethics committee applications.
• Maintain study documentation, including monitoring visit reports, correspondence, and regulatory binders.
• Participate in investigator meetings, training sessions, and other study-related activities.
• Ensure patient safety and the integrity of clinical data throughout the study.
• Assist in the development and review of study protocols, informed consent forms, and other study-related documents.
• Provide regular updates and reports to the Clinical Research Manager/Director.

Qualifications:

• Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred.
• Minimum of 1 year of experience in clinical research, with a focus on oncology.
• In-depth knowledge of GCP, FDA regulations, and ICH guidelines.
• Strong understanding of clinical trial processes and documentation.
• Excellent organizational and time-management skills.
• Exceptional attention to detail and accuracy.
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.
• Proficiency in MS Office and clinical trial management systems (CTMS).

To find out more about this opportunity, please contact Steffan Lian at Steffan.Lian@gmprecruit.com

We regret that only shortlisted candidates will be notified.

GMP Recruitment Services (S) Pte Ltd | EA Licence : 11C3793 | Lian Cher Chieh | Registration No: R 1217705

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