About Company
At Hiring.zycto, we believe that groundbreaking clinical research is the cornerstone of future healthcare. We are a dynamic and forward-thinking organization dedicated to advancing medical science through meticulous, patient-centric studies. For a Clinical Research Coordinator, our environment offers unparalleled opportunities to contribute directly to life-changing discoveries. Join a collaborative remote team where your attention to detail, commitment to ethical research, and passion for improving patient outcomes will be recognized and celebrated. We empower our CRCs with the tools and support needed to excel, ensuring both professional growth and work-life balance in a vital field.
Job Description
Hiring.zycto is seeking a dedicated and meticulous Clinical Research Coordinator to join our innovative remote team. This is an exceptional opportunity for a detail-oriented professional passionate about contributing to cutting-edge medical research from anywhere in Canada. As a Remote Clinical Research Coordinator, you will be instrumental in the successful execution of clinical trials, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and regulatory requirements. You will manage crucial aspects of participant recruitment, consent, scheduling, and data collection, all while maintaining rigorous quality standards and patient safety.
We are looking for someone who thrives in a collaborative, remote environment, possessing strong organizational skills, excellent communication abilities, and a proactive approach to problem-solving. Your expertise will directly impact the advancement of new therapies and treatments, making a tangible difference in patients’ lives. This role requires a high degree of independence, a commitment to ethical research, and proficiency with clinical trial management systems. If you’re ready to leverage your clinical research acumen in a flexible, impactful setting, Hiring.zycto offers a supportive culture and exciting challenges.
Key Responsibilities
- Coordinate and manage all aspects of assigned clinical trials from study start-up through close-out, ensuring compliance with protocol, GCP, ICH guidelines, and all applicable regulatory requirements.
- Facilitate the informed consent process with study participants, ensuring a clear understanding of the study purpose, procedures, risks, and benefits.
- Recruit, screen, and enroll eligible study participants according to protocol criteria and maintain accurate enrollment logs.
- Schedule and conduct remote study visits, assessments, and follow-ups with participants, utilizing tele-health platforms and other digital tools as appropriate.
- Collect, record, and maintain accurate and complete study data in electronic Case Report Forms (eCRF) or other data capture systems, resolving queries promptly.
- Manage and reconcile study-specific documentation, including source documents, regulatory binders, and essential documents.
- Report adverse events (AEs) and serious adverse events (SAEs) in a timely manner to the Principal Investigator, sponsor, and Institutional Review Board (IRB)/Ethics Committee (EC) as per protocol and regulatory requirements.
- Maintain effective communication with study participants, investigators, sponsors, and other research personnel, facilitating a smooth trial process.
- Assist with regulatory submissions, IRB/EC correspondence, and ongoing review processes.
- Participate in sponsor monitoring visits and audits, providing necessary documentation and explanations.
- Ensure the proper handling, storage, and accountability of investigational products and supplies.
- Stay current with clinical research best practices, regulations, and relevant therapeutic area knowledge.
Required Skills
- Minimum of 3 years of experience in clinical research coordination or a related role.
- Demonstrated understanding and application of Good Clinical Practice (GCP) and ICH guidelines.
- Proficiency with Electronic Data Capture (EDC) systems, eCRFs, and clinical trial management software.
- Exceptional organizational skills and meticulous attention to detail.
- Strong verbal and written communication skills for interacting with diverse stakeholders (participants, investigators, sponsors).
- Ability to work independently, manage multiple priorities, and meet deadlines in a remote work environment.
- Technically proficient with virtual communication tools (e.g., video conferencing, secure messaging platforms).
- Bachelor’s degree in a health-related field (e.g., Nursing, Life Sciences, Public Health).
Preferred Qualifications
- Certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA).
- Master’s degree in a relevant field.
- Experience in specific therapeutic areas pertinent to Hiring.zycto’s research portfolio (e.g., Oncology, Cardiology, Neurology).
- Familiarity with Health Canada regulations and other international regulatory bodies.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- Generous paid time off and holidays.
- Flexible remote work schedule.
- Opportunities for professional development and continuous learning.
- Supportive and collaborative team culture.
- Access to cutting-edge research and technology.
How to Apply
Interested candidates are encouraged to apply by clicking the link below. Please ensure your resume and a cover letter detailing your relevant experience and qualifications are attached. We look forward to reviewing your application and exploring how your expertise can contribute to our team.