Job Description
Position Overview
The Project Manager Patient Engagement works closely with the Scientific Patient Engagement & Advocacy Lead and is responsible for the strategic planning coordination operational excellence leading to execution of all patient engagement activities. This includes managing and planning congress activities patient speaker engagements patient dialogue initiatives direct engagements with consultants and organizing both small and large meetings with patient advocates. The ideal candidate possesses strong organizational skills exceptional communication abilities and experience working with patient communities in a healthcare or life sciences setting. The candidate must be able to plan lead and facilitate the execution of patient engagement activities within a cross-functional team utilizing their network to influence and ensure completion of activities in a compliant manner.
Key Responsibilities
Patient Engagement Activities within Patient Innovation and Engagement team such as:
Congress Activities Management: Oversee all aspects of patient involvement at medical and scientific congresses including planning logistics contract support and on-site coordination. Ensure patient perspectives are meaningfully integrated into congress programming.
Patient Speaker Engagements: Identify recruit and support patient speakers for internal and external events. Coordinate speaker training logistics and follow-up to ensure impactful and compliant engagements.
Patient Dialogue Activities: Facilitate and support the vendor assignment and operational activities that foster dialogue between patients advocates and company stakeholders. Ensure action memo tracking in adobe sign capture insights and feedback to inform organizational strategies for activities.
Patient Advocate Meetings: Plan and execute small and large meetings with patient advocates including roundtables advisory boards and community forums. Manage invitations agendas materials and post-meeting communications.
Stakeholder Collaboration: Work closely with cross-functional teams (medical affairs communications regulatory GEMs etc.) to ensure alignment and compliance in all patient engagement initiatives.
Compliance and Reporting: Ensure all activities adhere to relevant legal regulatory and ethical standards. Maintain accurate documentation and generate reports on engagement outcomes.
Qualifications
Bachelors degree in life sciences communications public health or a related field (Masters or higher preferred).
Experience and background in managing and planning congress activities.
5 years of experience in project management preferably in patient engagement advocacy or healthcare communications.
Strong organizational and multitasking skills with a proven track record of managing complex projects.
Excellent interpersonal and communication skills with the ability to engage and build trust with diverse stakeholders.
Experience working with patient communities advocates or patient organizations is highly desirable.
Understanding of compliance requirements and best practices in patient engagement.
Proficiency in project management software and virtual meeting platforms.
Ability to travel as needed for congresses meetings and events.
Key Competencies
Empathy and cultural sensitivity
Attention to detail
Strategic thinking and problem-solving
Adaptability and resilience
Collaboration and teamwork
Required Skills:
Clinical Engagement Clinical Engagement Collaborative Development Contract Lifecycle Management (CLM) Contract Management Digital Project Management Ethical Standards Healthcare Education Healthcare Project Management Innovation Projects Knowledge Management Leadership Legal Compliance Life Science Medical Affairs Medical Communications Medical Knowledge Medical Operations Operational Excellence Patient Communications Patient Engagement Professional Networking Project Management Project Management Software (PMS) Results-Oriented 5 morePreferred Skills:
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U.S. Hybrid Work Model
Effective September 5 2023 employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week Monday - Thursday although the specific days may vary by site or organization with Friday designated as a remote-working day unless business critical tasks require an on-site Hybrid work model does not apply to and daily in-person attendance is required for field-based positions; facility-based manufacturing-based or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note this Hybrid work model guidance also does not apply to roles that have been designated as remote.
The salary range for this role is
$187000.00 - $294400.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive if applicable.
We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance
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Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
25%Flexible Work Arrangements:
HybridShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
12/4/2025*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
Required Experience:
Director
Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more