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Job Title


Integration Procedural Documentation Manager-Clinical Research


Company : Jobrapido


Location : Saskatoon, Saskatchewan


Created : 2026-04-17


Job Type : Full Time


Job Description

ICON plc., (is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. Working with our Sponsor''s SOP Acquisition Lead to assist in the coordination of the assessment and transition plan for possible integration of procedural documentation into the Sponsor''s SOP model for clinical, medical, safety, regulatory, and quality management system processes relating to business deals. JOB RESPONSIBILITIES Indicate the primary responsibilities critical to the job. Developing SOP mapping between Sponsor''s SOPs and the acquirees Sponsor/CRO vendor procedural documentation Conduct comparison assessments between the procedural documentation to identify major gaps and work with the business process owner and SOP authors to validate Facilitate the risk assessment of gaps with the business and document any interim procedures to mitigate the risk Develop the official transition communication (using templates) Develop the retirement strategy ORGANIZATIONAL RELATIONSHIPS Provide the primary groups or key role(s) that this role will have interaction with as a regular part of the Job responsibilities. Include any external interactions as appropriate. Head of SOPs Sponsor''s SOP Acquisition Lead Sponsor''s Business Process Owners (BPOs) for clinical, medical, safety, regulatory and quality management system process areas Sponsor''s SOP Authors for clinical, medical, safety, regulatory and quality management system process areas Quality organization colleagues Sourcing Risk & Compliance Project Management Office (PMO) Colleagues (PMOs are established per business deal) QUALIFICATIONS / SKILLS Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications and other job-related technical and managerial skills. BS/BA Degree plus 5+ years Pharma experience. Demonstrated experience in project management and implementation techniques. GxP experience and a strong working knowledge and understanding of drug development processes. TECHNICAL SKILLS REQUIREMENTS Indicate the technical skills required and/or preferred, as applicable. Required: Proficient in Microsoft applications (i.e., Word, Excel, PowerPoint, TEAMS, MS Project) What ICON can offer you: 21 days of company vacation (PTO) per year (prorated), plus public/statutory holidays observed in your state. A range of health insurance offerings to suit you and your familys needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Program, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your familys well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. At ICON, inclusion & belonging are fundamental to our culture and values. Were dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.