Associate Director, Project Management - Drug Development (Hybrid)
USA - Pennsylvania - North Wales (Upper Gwynedd)
Job Description
Job Description:
The drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division organization of our company.
Position Description/Summary:
The GPAM Associate Director, Project Manager, is a core member of Early Drug Development and/or Late Drug Development Teams, partnering with team leaders to develop strategies and execute our Company's drug and vaccine development efforts to progress the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive cross-functional teams with sufficient influence and mastery of project management to take on challenging assignments with minimal guidance. Projects could span any therapeutic areas in which our company is actively engaged. In addition to project work, the Associate Director is expected to contribute to ongoing business process improvement and talent development in Global Project and Alliance Management (GPAM).
Primary Responsibilities:
Managing the end-to-end drug development process, including projects of significant complexity; driving cross-functional teams and leading by influence to develop comprehensive strategies and ensure successful execution.
Act as enterprise leaders by guiding teams through the creation, approval, and execution of integrated project plans appropriate to the project's phase of development and complexity. This includes integrating strategic and tactical input from diverse disciplines (e.g., clinical, regulatory, market access, manufacturing, CMC, commercial, and other areas) as applicable to the project.
Building and maintaining project schedules and critical project information in enterprise project management systems and databases. Using these tools to integrate activities across key team members, proactively identify risks, and ensure clear and effective communication with key team, management, and cross-departmental stakeholders.
Leveraging relationships and networks to improve and enhance team dynamics; proactively identifying and removing obstacles to drive business results.
Navigating our company's process and organizational norms to enable teams to understand corporate governance and business requirements, thereby enabling decision-making.
Leading key team meetings including creating thoughtful agendas, ensuring appropriate participation, contributing project management insights, and following up to ensure the team continues to make progress while holding others accountable.
Participating in Global Project and Alliance Management (GPAM) departmental initiatives and workstreams aimed at improving the way that we work and the way that we interact with one another as well as other departments. Improving business processes to find new efficiencies and connect people to the information that they need.
Providing mentoring, coaching, and oversight to Specialist and Senior Specialist project managers working on common projects. Sharing lessons learned and best practices to impact the Global Project and Alliance Management (GPAM) community positively.
Required Education, Experience, and Skills:
Bachelor’s degree required; concentration in a scientific or applied discipline preferred
Minimum of five (5) years of experience in project management or a related role required
Product development experience required; in a pharmaceutical/biotech industry preferred
Preferred Experience and Skills:
Advanced degree (e.g., MS, MBA, Ph.D., PharmD) preferred
Experience and knowledge of clinical drug development strongly preferred; including the different phases of development and how the various functional areas contribute to a comprehensive strategy
Project management certification (PMP) and/or formal coursework/training in project management strongly preferred
Required Travel:
Minimal
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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 presence.This 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 Company is required to provide a reasonable estimate of the salary range for this job in certain states and cities within the United States. Final determinations with respect to salary will take into account a number of factors, which may include, but not be limited to the primary work location and the chosen candidate’s relevant skills, experience, and education.
Expected US salary range:
$135,500.00 - $213,400.00Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here.
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:
DomesticVISA Sponsorship:
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25%Flexible Work Arrangements:
HybridShift:
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12/9/2024*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
ApplyJob Profile
Hybrid Hybrid work Hybrid work model On-site Puerto Rico residents only US and Puerto Rico residents only
Benefits/PerksBonus eligibility Diverse workplace Equal opportunity employer Flexible work Flexible work arrangements Health Care Hybrid work Hybrid work model Inclusion Inclusive environment Insurance Meetings Mentoring Paid holidays Retirement benefits Sick Days Vacation
Tasks- Coaching
- Communication
- Compliance
- Develop project plans
- Develop strategies
- Drive cross-functional teams
- Effective Communication
- Execution
- Governance
- Identify risks
- Improve business processes
- Innovation
- Leadership
- Manage drug development process
- Mentoring
- Mentor project managers
- Process Improvement
- Project management
- Talent Development
Access Best Practices BioTech Biotech industry Business Processes Business Process Improvement Clinical Clinical drug development CMC Coaching Commercial Communication Compliance Cross-functional Team Leadership Cross-functional Teams Databases Development Drug Development Education Effective Communication Enterprise project management systems Execution Governance Inclusion Influence Innovation Leadership Management Manufacturing Market Access Mentoring MS Organization Organizational Pharmaceutical PharmD PMP Process Improvement Product Development Project Management Regulatory Research Risk Management Strategic planning Strategy Talent Development Teams Therapeutic Areas Training Vaccine Development
Experience5 years
EducationAdvanced degree AS Associate Bachelor Bachelor's degree Business Certification Health Care Management MBA MS Pharm.D Ph.D.
CertificationsMBA PMP Project Management Certification
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9