Clinical Research Coordinator Jobs

About The Position

Requirements

• Bachelor’s degree or equivalent and relevant formal academic or vocational qualification.
• Previous experience providing relevant knowledge, skills, and abilities comparable to 2+ years.
• Solid understanding of the clinical research process, including GCP, SOPs, informed consent, and safety monitoring.
• Ability to work independently, analyze information, maintain attention to detail, prioritize sensitive and complex information, and solve problems.
• Ability to exercise discretion and sound judgment.
• Good decision-making, negotiation, and influencing skills.
• Good organizational skills.
• Good proficiency in basic computer applications.
• Good interpersonal skills and ability to work in a team environment.
• Regular and consistent attendance.
• Ability to work upright and/or stationary for 6–8 hours per day; perform repetitive hand movements; and meet mobility, bending, twisting, and occasional crouching or stooping demands.
• Ability to lift and carry objects; the physical requirements specify a maximum of 15–20 lbs, while the work schedule/environment section states ability to lift 40 lbs without assistance.
• Ability to communicate and understand information presented verbally, interact with diverse groups, multitask, and perform under stress.

Nice To Haves

• BLS certificate preferred.
• English fluency is an advantage.

Responsibilities

• Conduct clinical studies according to FDA/GCP and ICH regulations and guidelines.
• Provide medical care to patients while prioritizing patient safety.
• Schedule subject visits within protocol windows and help maximize scheduling capacity.
• Perform study activities such as informed consent, screening, vital signs, pregnancy tests, height and weight measurements, and ECGs.
• Record patient information and test results on required protocol forms.
• Complete investigational product accountability logs and related information where required.
• Report suspected non-compliance to relevant site staff.
• Ensure IRB approval is obtained before study initiation and that IRB requirements are met throughout the study.
• Promote the company and build positive patient relationships to support retention.
• Attend site initiation and other relevant meetings for protocol training.
• Call patients, book appointments, and make follow-up calls to confirm bookings or provide information or results when required.
• Enter and complete accurate information in sponsor systems, including case report forms and EDC, within required timeframes.
• Gather and maintain source documents, update patient files and notes, and keep records current.
• Adhere to company COP/SCOP.
• Dispose of waste according to standards and help maintain the facility’s general appearance when required.