About Company
Leading innovation in pharmaceutical discovery, Hiring.zycto offers a dynamic and collaborative environment where scientific rigor meets patient-centric development. For a Clinical Research Manager, this means direct involvement in groundbreaking trials, shaping the future of medicine with a team dedicated to excellence. We foster leadership and empower our experts to drive impactful clinical strategies, ensuring every project contributes meaningfully to global health. Join us to advance your career at the forefront of pharmaceutical research.
Job Description
Hiring.zycto is actively seeking a highly skilled and motivated Clinical Research Manager to join our pioneering pharmaceutical team in Toronto’s vibrant Harbourfront. In this critical role, you will be instrumental in overseeing the planning, execution, and completion of clinical trials across various therapeutic areas. This is a fantastic opportunity for a seasoned professional to make a significant impact on our drug development pipeline, ensuring adherence to regulatory standards, ethical guidelines, and company objectives.
As a Clinical Research Manager, you will be the driving force behind our clinical studies, managing multi-disciplinary teams and complex projects from protocol development through study close-out. Your expertise will be vital in navigating the intricate landscape of clinical research, maintaining impeccable data quality, and fostering strong relationships with investigators, sites, and internal stakeholders. We are looking for a leader who can not only manage but also inspire, mentor, and strategize, contributing to a culture of continuous improvement and scientific excellence. You will be expected to identify potential risks and develop mitigation strategies, ensuring trials are delivered on time, within budget, and to the highest scientific and ethical standards. This role demands meticulous attention to detail, strong problem-solving capabilities, and a deep understanding of the pharmaceutical industry’s regulatory framework. Join us at Hiring.zycto and contribute to bringing life-changing therapies to patients worldwide.
Key Responsibilities
- Manage and oversee all operational aspects of assigned clinical trials from study start-up to close-out, ensuring compliance with ICH-GCP guidelines, local regulations, and company SOPs.
- Develop, review, and approve study protocols, informed consent forms, CRFs, and other essential study documents.
- Lead and mentor a team of clinical research associates and other trial personnel, fostering a collaborative and high-performing environment.
- Manage trial budgets, timelines, and resources effectively, identifying and mitigating potential risks.
- Oversee vendor selection and management (e.g., CROs, central labs), ensuring quality deliverables and adherence to contracts.
- Facilitate communication and collaboration with investigators, site staff, internal departments (e.g., Regulatory Affairs, Medical Affairs), and external partners.
- Ensure accurate and timely data collection, monitoring quality, and participating in data review and interpretation.
- Prepare and present study updates, progress reports, and results to internal and external stakeholders.
- Participate in the development and implementation of departmental policies, procedures, and training programs.
Required Skills
- Minimum of 5 years of experience in clinical research, with at least 2 years in a management or lead role within the pharmaceutical or biotechnology industry.
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related scientific field.
- Thorough knowledge of ICH-GCP guidelines, Health Canada regulations, and other relevant regulatory requirements.
- Demonstrated ability to manage complex clinical trials, including budget and timeline management.
- Strong leadership, team management, and mentoring skills.
- Excellent written and verbal communication, presentation, and interpersonal skills.
- Proficiency in clinical trial management systems (CTMS), electronic data capture (EDC), and Microsoft Office Suite.
- Proven problem-solving abilities and a proactive approach to issue resolution.
Preferred Qualifications
- Master's degree or Ph.D. in a relevant scientific discipline.
- Certification as a Clinical Research Professional (e.g., SoCRA, ACRP).
- Experience across multiple therapeutic areas, particularly in oncology, rare diseases, or immunology.
- Familiarity with global clinical trial operations and international regulatory submissions.
- Experience with submission of clinical trial applications to regulatory authorities.
Perks & Benefits
- Comprehensive health, dental, and vision insurance package.
- Generous paid time off and flexible work arrangements.
- Competitive salary with performance-based bonuses.
- Retirement savings plan with company match.
- Professional development and continuing education opportunities.
- On-site fitness center and wellness programs.
- Collaborative and inclusive work environment in a prime downtown location.
- Opportunity to work on cutting-edge research and impact patient lives.
How to Apply
Interested candidates are encouraged to apply by clicking on the application link below. Please submit your resume and a cover letter detailing your relevant experience and why you are the ideal candidate for this role. We thank all applicants for their interest, however, only those selected for an interview will be contacted.