Senior Program Manager - Medical & Clinical Affairs

Convatec Group PLC

$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering or Science; advanced degree preferred
  • 7+ years of experience managing technical projects in medical device and/or pharmaceutical sectors
  • Project management qualification (PMP, APM, or equivalent) preferred
  • Experience with clinical study execution in medical devices is desirable
  • Strong understanding of Clinical Research Trials and their ethical considerations

Responsibilities

  • Manage clinical studies to ensure timely completion within scope and budget
  • Collaborate with cross-functional teams to ensure coordinated execution of clinical projects
  • Organize and manage clinical portfolio activities, identifying necessary resources and sequencing them appropriately
  • Integrate and plan workstreams into master study schedules aligned with business needs
  • Communicate study updates to stakeholders, particularly the Head of Clinical Operations
  • Review and revise study schedules with senior management and project teams for successful completion
  • Proactively identify risks and resolve project issues efficiently
  • Document and secure all study-related information effectively

Benefits

  • Remote work flexibility for US-based candidates
  • Opportunities for professional development and career growth
  • Access to a collaborative and inclusive team environment
  • Travel opportunities within the United States and Europe for project-related needs
  • Health and wellness programs to support employee well-being
Full Job Description
Position Overview:

As part of the Project and Portfolio Management team for Medical and Clinical Affairs, the Sr Program Manager oversees the project management, planning, execution, tracking, and reporting of clinical studies and/or research projects in accordance with agreed upon resourcing, timing, and budget. This individual drives cross functional project and/or program execution through collaboration with a wide range of functional groups across Convatec.

This is a remote US-based role.

Key Responsibilities:
  • Consistently project manage clinical studies to ensure completion on time within the agreed scope and budget
  • Work with cross functional management, clinical operations teams, and project teams to provide a coordinated and collaborative approach to executing the clinical studies
  • Organize and manage the clinical portfolio activities to identify and sequence the activities needed to successfully complete each study and establish the resources (time, money, functions, etc.) required to complete the activities
  • Work within a cross functional team to ensure workstreams are appropriately planned and integrated into master study schedules, and are aligned with the target business need
  • Develop communication plans and provide updates on assigned studies to stakeholders, specifically with the Head of Clinical Operations
  • Review study schedules with senior management, clinical operations team members, and project team members; revise schedules/plan as required to ensure successful completion
  • Proactively identify and mitigate project risks. Escalate as appropriate to ensure timely resolution of identified issues
  • Set up files to ensure all study information is appropriately documented and secured
  • Support the PMO (Program Management Office) to develop and enhance project management tools, processes, and systems to ensure consistent and efficient ways of working


Skills & Experience:
  • Strong proficiency in the use of MS Word, MS Project, MS Excel, MS PowerPoint, MS Teams, database software, SAP, MS Outlook, Project Management Cloud Software
  • Strong communicator; Speak, listen and write in a clear, thorough and timely manner using appropriate and effective communication tools and techniques.
  • Leader and team-worker who actively looks to develop themself and others; proactively networks across a complex organizational hierarchy and works cooperatively and effectively with others to set goals and resolve problems
  • An active listener and connector. The ideal candidate can take the broader picture and the perspective of others into account, activating the right plan based on holistic understanding of the business challenges and business needs
  • Tenacity and sense of urgency; the ability to make things happen quickly with large, less nimble partners and/or teams. and make clear decisions which are timely and in the best interests of the organization.
  • Problem solver: Assess situations & conflicts to identify causes, gather and process relevant information, generate possible solutions, and make recommendations and/or resolve the problem.
  • Positively influence others and manage stakeholders to achieve results that are in the best interest of the organization.
  • Strong experience driving culture of "Execution Excellence" and accountability
  • Good understanding of Clinical Research Trials
  • Good balance of 'technical' and 'commercial' understanding
  • Proven experience in project planning & managing complex technical elements of development projects or clinical studies
  • Understand ethical behavior and business practices
  • Ability to manage workload in either site-based location(s), or a home environment utilizing video-based meeting platforms and online project management tools


Qualifications/Education:
  • Bachelor's degree in Engineering or Science; advanced degree preferred
  • 7+ years of experience successfully managing technical projects within a medical device and/or pharmaceutical company
  • Project management qualification is preferred (PMP, APM, or equivalent)
  • Prior experience with clinical study execution within medical devices desirable

Dimensions:

Team

No direct reports

Principal Contacts & Purpose of Contact

MACA (Medical and Clinical Affairs) organization to exchange information and coordinate action; T&I (Technology & Innovation) Finance and strategy team to exchange information and coordinate action, R&D to exchange information.

Travel Requirements

Position may involve travel up to 10% of the time, within the United States and Europe. Most trips will include overnight travel.

Languages
  • Speaking: Yes English
  • Writing/Reading: Yes English


Ready to join us?

At Convatec, we're pioneering trusted medical solutions to improve the lives we touch. If you're ready to make a real impact, apply today and help us bring our Forever Caring promise to life.

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Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you're unsure, please contact us at [redacted].

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