Vice President, Medical Affairs

Job not on LinkedIn

🕒 September 18

🏈 North America – Remote

⏰ Full Time

🔴 Lead

👔 Vice President

👻 Ghost score 18%

What it means: the chance that no one is really hiring for this job.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

• Develop and execute the long-term strategic vision for the Medical Affairs division with the CMSO • Own the operating budget and P&L for Medical Monitoring and Pharmacovigilance • Build capability roadmaps for Medical Monitoring and Pharmacovigilance • Represent Medical Affairs on the Operational Leadership Team and advise the CMSO on medical, scientific, and safety risks • Drive collaboration across Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, Quality Assurance, Scientific Affairs, and Business Development • Provide executive oversight of medical monitoring across Indero's clinical trial portfolio • Lead physician resourcing, including hiring, training, deployment, and performance management • Maintain medical monitoring SOPs, work instructions, and quality standards • Escalate complex or high-risk medical monitoring issues and sponsor-facing medical disputes • Provide strategic and operational oversight of pharmacovigilance, including case processing, signal detection, aggregate reporting, and regulatory submissions • Ensure compliance with global and country-specific pharmacovigilance obligations • Lead readiness for PV regulatory inspections and internal audits • Partner with sponsors on PVAs and SDEAs • Partner with Business Development on RFPs, client presentations, bid defenses, pricing, and new business • Serve as senior medical point of contact for key sponsor accounts • Represent Indero in scientific and industry forums • Ensure Medical Affairs compliance with regulations, the QMS, and sponsor requirements • Own Medical Affairs SOPs, quality plans, CAPA plans, and audit/inspection responses at executive level • Lead, mentor, and develop the multidisciplinary Medical Affairs team • Establish workforce planning, career pathing, succession planning, leadership development, performance frameworks, and KPIs

🎯 Requirements

• Medical doctor (MD, DO, or equivalent international medical degree) required • 12-15 years of progressive experience in the pharmaceutical, biopharmaceutical, or clinical research industry • 5-7 years in a leadership role within a CRO, pharmaceutical company, or hybrid organization • Demonstrated experience leading and scaling Medical Monitoring and Pharmacovigilance functions • Proven track record of client engagement in a commercial, revenue-generating environment • Deep expertise in global clinical trial regulatory frameworks • Meaningful exposure to multiple therapeutic areas • Experience with health authority interactions, regulatory inspections, and audit defense • Experience managing P&L or budget responsibility • Board certification in dermatology or rheumatology is an asset but not required • Advanced business training (e.g., MBA) is an asset but not required • Working knowledge of PV safety databases and safety reporting automation tools • Exposure to AI-assisted technologies in medical monitoring, PV, or medical writing workflows • Published authorship of peer-reviewed scientific manuscripts or presentations at major clinical/scientific conferences • Multilingual capability or international regulatory experience • Ability to legally work in North America • Willingness to travel frequently

🏖️ Benefits

• Competitive compensation with performance incentives • Full benefits • Attractive advancement opportunities • Stimulating work environment • Remote role with frequent travel

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