Clinical Trial Manager II

Job not on LinkedIn

🕒 July 11

🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

🔴 Lead

🧪 Clinical Research

👻 Ghost score 42%

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

• Responsible for the operational management and oversight of clinical investigative sites • Ensures that clinical monitoring activities are performed correctly and timely • Identifies quality issues and trends related to site performance • Serves as a point of contact for CRAs and Lead CRAs for assigned projects • Provides mentoring and oversight of CRAs and Lead CRAs • Prepares and conducts project-specific training for the CRAs • Develops annotated site visit reports and monitoring tools • Coordinates and leads CRA meetings

🎯 Requirements

• B.Sc. in a field relevant to clinical research, nursing degree and/or equivalent experience • At least 8 years of clinical research experience including prior monitoring experience • At least 2 years of experience acting in a Lead CRA or Clinical Team Leader role in the biotechnology, pharmaceutical, and/or contract research organization (CRO) industry • Strong knowledge of ICH/GCP standards and applicable regulatory requirements • Excellent mastery of Microsoft Office suite (Word, Excel, Power Point) • Ability to work in a fast-paced evolving environment and establish good relationships with colleagues, sites and sponsors • Excellent leadership, organizational, time management and multi-tasking skills • Excellent judgement and problem-solving skills • Occasional travel (up to 10% of the time) • Fluent in English (excellent oral and written), French is an asset • Experience in a CRO and in dermatology an asset.

🏖️ Benefits

• Flexible work schedule • Complete benefits (medical, dental, vision, vacation, personal days, virtual medical clinic, social activities) • Ongoing learning and development