Job Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our new dynamic team. In this role, you will oversee and manage clinical trials, ensuring compliance with regulatory requirements and protocols. You will work closely with medical professionals, patients, and research staff to facilitate the successful execution of research projects. Your expertise in medical terminology and data management will be essential in analyzing research outcomes and maintaining accurate records.
With upcoming projects starting we will be looking to ramp up this position into a full time position.
Responsibilities
- Coordinate all aspects of clinical trials from initiation to completion, ensuring adherence to protocols and regulatory guidelines.
- Supervise and train research staff, including nurses and other team members involved in the study.
- Conduct patient assessments, including obtaining informed consent and performing phlebotomy as needed.
- Manage data collection processes, ensuring accuracy and integrity of research data.
- Analyze collected data to identify trends, outcomes, and areas for improvement in study protocols.
- Maintain comprehensive documentation of study activities, including participant records, regulatory submissions, and correspondence with sponsors.
- Collaborate with principal investigators to develop study protocols and implement necessary changes throughout the trial process.
- Ensure compliance with ethical standards and institutional policies related to human subject research.
Qualifications
- Bachelor’s degree in a relevant field; nursing degrees or Internal Medical Graduates ade preferred.
- Proven experience in clinical research coordination or a related role is strong asset.
- Strong understanding of medical terminology and clinical trial processes.
- Excellent organizational skills with the ability to manage multiple projects simultaneously.
- Proficient in data management systems and software for tracking research activities.
- Strong analytical skills with attention to detail for accurate data analysis.
- Ability to communicate effectively with diverse groups including patients, healthcare professionals, and regulatory bodies.
- Certification in Clinical Research (e.g., ACRP or SOCRA) is a plus but not required.
Join us in advancing medical knowledge through innovative research while making a meaningful impact on patient care!
Job Types: Part-time, Casual
Pay: From $52,422.16 per year
Expected hours: 25 – 40 per week
Application question(s):
- Are you an International Medical Graduate?
Education:
- Bachelor's Degree (preferred)
Experience:
- Clinical Trial : 1 year (preferred)
Work Location: In person
