Project Manager II, Early Phase

Job not on LinkedIn

🕒 August 21

🇵🇱 Poland – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 26%

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

• Lead the initiation, planning, execution, monitoring, control, and closure of assigned Phase I and Phase II clinical trials • Act as the main point of contact for sponsors, vendors, and internal study teams throughout the clinical trial lifecycle • Coordinate study resources, deliverables, timelines, budgets, scope, and clinical operations activities • Support feasibility, study design, budget development, progress reporting, and operational planning • Maintain communication with sponsors, study teams, functional departments, clinical sites, and senior management • Monitor study budgets, billed time, out-of-scope activities, and change order management • Lead study start-up activities, including kick-off meetings, TMF setup, site selection and activation, vendor onboarding, site contracting, and budget negotiations • Identify and manage risks, implement quality control measures, and escalate issues as necessary • Lead client, internal team, and vendor meetings; document and file meeting minutes • Oversee project deliverables, vendor and subcontractor outputs, and continuous improvement initiatives • Maintain study-specific training matrices and verify project training and records • Review and approve responses to quality assurance audits • Ensure protocols, informed consent forms, eCRFs, source document templates, TLFs, and clinical study reports are completed on schedule • Oversee TMF filing, maintenance, archiving, completeness, accuracy, and inspection readiness • Track recruitment performance and develop enrollment mitigation plans • Participate in Investigator Meetings and coordinate ethics submissions with Regulatory Affairs • Support study sites and ensure they have necessary materials and resources • Collaborate with Data Management on CRFs, data review, query resolution, and database lock • Partner with Clinical Operations on monitoring activities and sponsor, SOP, regulatory, GCP, and study requirements • Contribute to Clinical Monitoring Plans and provide project-specific CRA training • Conduct site initiation visits for single-site studies when needed • Develop annotated site visit reports and monitoring tools • Mentor junior staff and support onboarding • Provide technical, therapeutic, and project management expertise for departmental training and process improvement • Participate in business development activities and contribute to operational tools and process improvement initiatives

🎯 Requirements

• A Bachelor's degree (B.Sc.) in a field related to clinical research • At least 5 years of experience in the clinical research industry • Minimum of 3 years of project management experience in Phase I and Phase II clinical trials • Experience managing multiple clinical trials simultaneously across several study sites • Previous experience in dermatology clinical trials, strongly preferred • Strong knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, FDA requirements, and applicable local regulations • Proficiency with the Microsoft Office Suite • Excellent written and verbal communication skills in English • Bilingualism in English and French is highly desirable • Ability to work effectively in a collaborative team environment and build strong relationships with colleagues, sponsors, and other stakeholders • Strong problem-solving, critical-thinking, and creative-thinking skills • Solid scientific understanding and clinical research knowledge • Broad cross-functional knowledge of clinical research operations • Ability to manage multiple projects, prioritize competing demands, and perform effectively under pressure while meeting deadlines • Knowledge of Good Clinical Practices as well as applicable Health Canada and FDA regulations and guidelines • Legally authorized to work in Poland

🏖️ Benefits

• Permanent full-time position • Vacation • PPK • Health allowance • Home-based position with teleworking allowance • Ongoing learning and development • Attractive advancement opportunities