Senior Clinical Research Coordinator – Oncology

• Perform study start-up duties, including recruitment plans, recruitment tools, progress notes, and phone screening
• Plan logistical needs for clinical trials and assist CRC Level I and Level II staff with trial planning and conduct
• Evaluate recruitment needs, communicate recruitment efforts, and execute plans to generate randomized patients and maximize retention
• Attend investigator meetings
• Maintain Clinical Trial Management System skills and update databases, reimburse participants, capture referral sources, and create recruitment call lists
• Perform protocol-specific clinical procedures and train others on technical requirements
• Review patient inclusion and exclusion criteria during screening
• Document laboratory data and adverse reactions and notify investigators, the Institutional Review Board, and sponsors of serious adverse events
• Dispense study medication at the Investigator’s direction
• Establish relationships with patient volunteers, provide patient education, and conduct informed consent
• Communicate patient, recruitment, and clinical status to investigators and sponsoring-company monitors
• Maintain relationships with monitors and sponsors and promote the site for future trials
• Prospect for new business and develop physician relationships
• Monitor and review other coordinators and support staff
• Attend site evaluation visits as a senior staff representative
• Assist with training and development of site personnel
• Travel to other Duly sites within the Accellacare Site Network

Requirements

• Oncology clinical research industry experience
• 3+ years of experience as a Clinical Research Coordinator
• Clinical skills, such as phlebotomy
• Good understanding of clinical trial processes, GCP, and site documentation requirements
• Excellent time management and planning skills with an organized approach to work
• Bachelor’s degree in life sciences, healthcare, or a related field
• Legal right to work in the country where the role is based

Core Competencies

Demonstrates expertise in clinical trial management, including recruitment strategies, patient education, and adherence to GCP standards. Proficient in clinical procedures and capable of training staff while maintaining strong relationships with investigators and sponsors.

Highest-signal resume keywords

• Oncology Clinical Research Experience
• Clinical Research Coordinator Experience
• Phlebotomy Skills
• GCP Knowledge
• Time Management Skills

ATS Optimization Keywords

Hard Skills

• Clinical Trial Management
• Patient Recruitment
• Protocol-Specific Procedures
• Database Management
• Adverse Event Reporting
• Informed Consent Process
• Laboratory Data Documentation
• Study Medication Dispensing
• Screening Criteria Review
• Logistical Planning

Soft Skills

• Organizational Skills
• Communication Skills
• Relationship Building
• Training and Development
• Team Collaboration

Industry Keywords

• Clinical Trials
• Life Sciences
• Healthcare
• Patient Education
• Investigator Meetings
• Site Evaluation
• Retention Strategies
• Recruitment Plans
• Site Documentation Requirements
• Accellacare Site Network

Tools & Technologies

• Clinical Trial Management System