Research Associate

Job Summary Research Associate – Nuclear Medicine Division. The Research Institute of the McGill University Health Centre (RI‑MUHC) seeks a highly motivated and organized researcher to support a broad portfolio of clinical and translational studies investigating radiopharmaceuticals, imaging biomarkers, and nuclear medicine procedures. The role encompasses protocol implementation, data integrity oversight, statistical analysis, ethics and regulatory submissions, manuscript preparation, and support for commercialization efforts. Responsibilities Lead and conduct clinical and laboratory projects, including trials on radiopharmaceuticals, imaging biomarkers, and nuclear medicine procedures. Assess performance of tracers and imaging parameters on human physiological and clinical outcomes, supporting molecular and cellular research. Prepare quantitative datasets and perform biostatistical and computational analyses, using SPSS and other imaging analytics software. Support grant applications, progress reports, and technology transfer activities, providing documentation, validation, and regulatory preparation. Coordinate recruitment, informed consent, physiological assessments, imaging data acquisition, sample handling, and protocol-driven data collection in compliance with ICH‑GCP, TCPS‑2, PHIPA, and Health Canada/FDA regulations. Conduct literature reviews and draft manuscripts, abstracts, reports, visualizations, and presentations for peer‑reviewed journals and conferences. Design and lead research projects, including development, testing, and evaluation of advanced methodologies and protocols. Contribute to discovery, refinement, and validation of novel diagnostic or therapeutic agents in biomedical and nuclear medicine applications. Oversee clinical trial monitoring activities—site initiation, routine monitoring, and close‑out visits—ensuring data accuracy, protocol compliance, and participant safety. Maintain essential study documentation: CRFs, regulatory binders, SOPs, and quality control records. Submit ethics and regulatory documents supporting design and conduct of studies, including experimental protocols for radiopharmaceuticals and imaging investigations. Apply project‑management principles to scientific research workflows, monitoring timelines, resource allocation, and milestones. Verify data and conduct quality assurance activities to ensure research integrity and reproducibility. Collaborate with internal and external stakeholders, data teams, and clinical partners to support research data integrity and disseminate findings. Supervise assistants, technicians, junior scientists, trainees, students, volunteers, or other scientists as needed. Education & Experience PhD with >4 years postdoctoral experience in biomedical, clinical, or imaging research. Minimum 4 years of experience in clinical or translational research. Required Skills MD with >4 years experience in clinical and translational research, or a PhD with >4 years postdoctoral research experience, demonstrating advanced expertise in biomedical investigations. Strong publication record in peer‑reviewed journals (at least four first‑author papers). Excellent written and verbal communication in English; French an asset. Solid knowledge of quantitative and qualitative research methodologies and proven application in clinical contexts. Advanced proficiency in SPSS for data analysis. High‑level proficiency with Microsoft Office, ImageJ, Adobe Photoshop, EndNote, and other research tools. Strong analytical, critical‑thinking, and problem‑solving skills. Previous research experience in medical imaging, including participation in imaging‑based studies. Ability to work independently and collaboratively within multidisciplinary teams. Familiarity with research ethics, GCP, and institutional research policies. Sound judgment, discretion, and professionalism with confidential information. Excellent French and English—spoken and written. Excellent communication and interpersonal skills. Ability to work independently or with minimal supervision. Additional Information Status: Temporary, full time (35‑hour workweek) Pay Scale: $55,692.00 – $103,412.40, commensurate with education and experience. Work Shift: Variable Schedule Work Site: Hybrid, GLEN Site, 1001 boul. Decarie Cover letter: Please attach with your resume in one PDF document. Benefits 4‑week vacation, 5th week after 5 years 12 paid personal days (including sickness or family obligations) 13 paid statutory holidays Modular group insurance plan (includes gender affirmation coverage) Telemedicine services Defined benefit government pension plan (RREGOP) Training and professional development opportunities Child‑care centres Corporate discounts (OPUS + Perkopolis) Competitive monthly parking rate Employee Assistance Program Recognition Program Flexible work options Equal Opportunity Employment RI‑MUHC is committed to equity, diversity, and inclusion. Applicants from all backgrounds—racialized groups, visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and 2SLGBTQIA+ persons—are encouraged to apply. Those needing accommodations may confidentially contact research.talent@muhc.mcgill.ca. #J-18808-Ljbffr