Senior Program Manager – Medical & Clinical Affairs

Job not on LinkedIn

🕒 August 4

🏛️ District of Columbia, Florida, +3 more states – Remote

🏛️ District of Columbia – Remote 🐊 Florida – Remote 🌽 Illinois – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote

⏰ Full Time

🟠 Senior

📋 Program Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 23%

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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Convatec

WebsiteLinkedInAll Job Openings

5001 - 10000 employees

Founded 1978

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

Convatec is a global medical products and technologies company focused on therapies for the management of chronic conditions. Convatec leads in advanced wound care, ostomy care, continence care, and infusion care. The company is known for its innovative solutions like Hydrofiber® Technology and FeelClean Technology™, which enhance patient outcomes by improving comfort and care in conditions such as stoma and wound management. With a holistic approach, Convatec offers products and support programs through platforms like me+, aiming to empower individuals to live confidently with their conditions.

📋 Description

• Oversee project management, planning, execution, tracking, and reporting of clinical studies and/or research projects • Manage clinical studies to ensure completion on time, within agreed scope and budget • Coordinate with cross-functional management, clinical operations teams, and project teams • Organize and manage clinical portfolio activities, sequencing tasks and establishing required resources • Plan and integrate workstreams into master study schedules aligned with business needs • Develop communication plans and provide study updates to stakeholders, especially the Head of Clinical Operations • Review and revise study schedules and plans with senior management, clinical operations, and project teams • Identify and mitigate project risks and escalate issues for timely resolution • Set up and secure study documentation files • Support the PMO in developing and enhancing project management tools, processes, and systems

🎯 Requirements

• Strong proficiency in MS Word, MS Project, MS Excel, MS PowerPoint, MS Teams, database software, SAP, MS Outlook, and project management cloud software • Strong written and verbal communication skills • Leadership, teamwork, networking, and stakeholder management abilities • Problem-solving and decision-making skills • Strong experience driving a culture of “Execution Excellence” and accountability • Good understanding of clinical research trials • Balance of technical and commercial understanding • Proven experience planning and managing complex technical elements of development projects or clinical studies • Understanding of ethical behavior and business practices • Ability to manage workload in a site-based location or home environment using video-based meeting platforms and online project management tools • Bachelor’s degree in Engineering or Science required; advanced degree preferred • 7+ years of experience successfully managing technical projects within a medical device and/or pharmaceutical company • Project management qualification (PMP, APM, or equivalent) preferred • Prior clinical study execution experience within medical devices desirable • English required for speaking, writing, and reading

🏖️ Benefits

• Remote US-based role • Travel up to 10% of the time within the United States and Europe