Clinical Trial Delivery Trainer

Job not on LinkedIn

🔥 2 minutes ago

🇨🇦 Canada – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

201 - 500 employees

💊 Pharmaceuticals

🏥 Healthcare

💼 Consulting

Pharmaceuticals • Healthcare • Consulting

Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.

📋 Description

• Identify training and development needs across Clinical Trial Delivery • Develop and maintain role-based training curricula, onboarding pathways, and learning plans • Create, update, and standardize training materials, learning resources, assessments, and documentation • Maintain training content aligned with regulations, company procedures, systems, and operational practices • Develop and maintain a scalable Clinical Trial Delivery training repository • Recommend and implement training initiatives based on business needs, process changes, quality trends, and employee feedback • Deliver group and individual training programs for new and existing employees • Facilitate instructor-led, virtual, self-paced, and practical learning activities • Provide training on clinical trial processes, regulations, SOPs, systems, tools, and role-specific responsibilities • Coordinate refresher training • Support onboarding programs and define onboarding requirements and learning objectives • Monitor onboarding completion and support readiness assessments • Provide guidance to new employees during onboarding and role transition • Promote consistency in onboarding practices across functions and regions • Serve as trainer, mentor, and resource for Clinical Trial Delivery employees • Provide coaching and facilitate knowledge sharing and best-practice dissemination • Participate in competency observation and evaluation activities • Accompany CRAs on-site or remotely for observation and evaluation visits when appropriate • Coordinate and prioritize Coordinator Trainers’ daily activities • Contribute to training budget planning and provide cost estimates and business justifications • Evaluate training effectiveness using feedback, assessments, competency evaluations, and quality metrics • Improve training processes, content, tools, and delivery methods • Support new processes, technologies, and organizational initiatives through training and change management • Participate in developing and reviewing SOPs, work instructions, templates, and controlled documents • Provide updates and recommendations to Clinical Trial Delivery leadership

🎯 Requirements

• Bachelor’s degree in life sciences, nursing, clinical research, healthcare, education, or another relevant field, or an equivalent combination of education and experience • Minimum of 5 years of experience in clinical research within the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry • Previous experience in one or more Clinical Trial Delivery roles (e.g., Clinical Research Associate, Clinical Trial Manager, Project Manager, or other clinical operations or project delivery positions) • Experience delivering training, facilitating learning, coaching, mentoring, or supporting employee development • Experience developing training materials, onboarding programs, or role-based learning plans is an asset • Good knowledge of ICH-GCP, Health Canada, FDA, EMA, and other applicable regulatory requirements governing clinical research • Strong understanding of the clinical trial lifecycle, Clinical Trial Delivery processes, and cross-functional responsibilities • Ability to translate complex regulatory, operational, and technical information into practical and engaging learning experiences • Excellent presentation, facilitation, coaching, mentoring, and communication skills • Strong organizational, planning, prioritization, and time management skills • Comfortable working in evolving environments and adapting to new technologies, systems, and industry practices • Proficient in English, both written and spoken; proficiency in French or another language is an asset • Comfortable using AI-powered tools and productivity platforms (e.g., Microsoft Copilot, ChatGPT, Gemini, or similar technologies) • Willingness and ability to travel up to 10% of the time • Legally authorized to work in Canada

🏖️ Benefits

• Permanent full-time position • Flexible schedule • Vacation • Home-based position • Ongoing learning and development • Opportunities for advancement • Stimulating work environment