
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.
🔥 13 hours ago
Improve your chances of getting an interview by checking your resume score before you apply.

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.
• Serve as the primary contact for the Sponsor • Provide efficient and timely updates on trial progress • Lead client calls • Oversee and actively participate in preparation of study plans, protocols, informed consent forms, eCRFs, TLFs, and clinical study reports • Participate in planning and conducting Investigator Meetings • Ensure sites have necessary study materials, including investigational product, supplies, equipment, and safety lab kits • Ensure assigned studies are audit ready • Monitor the quality of study, vendor, and SubCRO deliverables and address issues • Manage risks and control measures to assure project quality • Analyze discrepancies between planned and actual results • Review and approve responses to quality assurance audits • Control project budgets, including internal hours allocated to activities • Identify out-of-scope activities for change orders • Manage trial timelines, budgets, resources, and vendors • Coordinate tasks and deliverables across functional departments • Communicate with study team members, functional departments, and senior management • Manage and report recruitment status and initiatives needed to meet recruitment timelines • Lead the core project team, including Associate Project Managers, Project Coordinators, and Project Assistants • Ensure project team members receive adequate training • Coordinate with Site Selection, Regulatory Affairs, Data Management, Clinical Monitoring, Biostatistics, and Scientific Affairs teams
• At least 7 years of global clinical project management experience, including management of all project phases from start-up to closure, all functional services, and vendor management • At least 10 years of industry experience, including a minimum of 3 years in a CRO • Experience with mid-size and large studies (>10–15 countries) in multiple regions (NA, SA, APAC, MENA, Europe) • Experience leading multicenter, multinational Phase III clinical trials, including project budget financial tracking and forecasting • B.Sc. in a related field of study to clinical research • PMP or PRINCE2 certification is an asset • Experience in study start-up, regulatory submission, resource management, supervisory experience, CRA, data management, medical writing, or vendor management is an asset • Therapeutic experience managing dermatology, onco-dermatology, rheumatoid arthritis, or oncology trials is an asset • Excellent knowledge of GCP and ICH standards and local country regulations • Excellent knowledge of Microsoft Office suite • Fluency in English with excellent oral and written skills is required • Bilingualism (English and local language) is an asset • Ability to work in a team environment and establish good relationships with colleagues and sponsors • Good problem-solving abilities • Strong ability to carry out different projects and work under pressure while meeting timelines
• Flexible schedule • Vacation • Home-based position • Ongoing learning and development opportunities • Stimulating work environment • Opportunities for growth and advancement
Apply Now🔥 19 hours ago
Biosampling Project Manager leading human biological sample management and central laboratory activities. Supporting ICON’s global clinical trials through vendor coordination, oversight, and issue resolution.
🔥 23 hours ago
Scrum Master leading Agile teams developing document-management software for clinical research. Coordinating delivery, facilitating ceremonies, and improving cross-team processes.
🇷🇴 Romania – Remote
💰 Private Equity Round on 2020-12
⏰ Full Time
🟡 Mid-level
🟠 Senior
👷♀️ Project Manager
🕒 Yesterday
Project Manager delivering infrastructure and IT operations projects for Software Mind’s global enterprise clients. Managing cloud, automation, observability and managed-service transition initiatives.
🇷🇴 Romania – Remote
💰 Private Equity Round on 2020-12
⏰ Full Time
🟡 Mid-level
🟠 Senior
👷♀️ Project Manager
🕒 5 days ago
Implementation Project Manager leading client implementations for Safeguard Global’s global employment and Managed Services solutions. Coordinating multi-country projects, risks, stakeholders, and transitions into ongoing service delivery.
🇷🇴 Romania – Remote
💵 lei245k / year
💰 Venture Round on 2019-05
⏰ Full Time
🟡 Mid-level
🟠 Senior
👷♀️ Project Manager
🕒 September 1
Project Manager delivering infrastructure and cloud operations projects for Software Mind’s enterprise clients. Coordinating teams, budgets, risk, stakeholder governance and managed-service transitions.
🇷🇴 Romania – Remote
💰 Private Equity Round on 2020-12
⏰ Full Time
🟡 Mid-level
🟠 Senior
👷♀️ Project Manager