Director, GRACS Business Development Execution, Regulatory Affairs

MSD

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profile Job Location:

Rahway, NJ - USA

profile Monthly Salary: $ 169700 - 267200
Posted on: 16 days ago
Vacancies: 1 Vacancy

Job Summary

Job Description

Under the minimal guidance of the Senior Director Business Development Execution the incumbent manages and is responsible for the business process and related activities associated with Global Regulatory Affairs and Clinical Safety (GRACS) Business Development Execution. The primary function includes coordinating various GRACS functional areas to ensure implementation and maintenance of regulatory activities associated with assigned Company Business Development (BD) Agreements. These agreements include but are not limited to divestitures mergers/acquisitions in-licensing out-licensing collaborations public private partnerships distribution co-marketing and authorized generic agreements. Facilitates the processes communications and governance to ensure GRACS contractual obligations and commitments are met while maintaining regulatory compliance.

  • Work closely with the Corporate Business Development our Companys Research & Development Division Global Alliance Management (MGAM) Integration Management Office (IMO) and GRACS Business Development to understand the partner agreements and the goals of those agreements throughout the lifecycle post signing.

  • Responsible for establishing the GRACS Integration or Transition Team (comprised of functional Subject Matter Expert (SME)) through the recruiting and onboarding integration team members upon completion of the due diligence and understanding of the contract execution requirements for the deal.

  • Following the GRACS Business Development Operating Model performs all responsibilities of the GRACS Business Development Execution Lead (or Integration Lead for Acquisitions/Mergers/Collaboration or Transition Lead for divestitures) including facilitation of discussions with GRACS SME execution team to identify gaps and risks track progress and coordinate ongoing updates of progress to ensure GRACS Leadership is informed as needed. Responsible for understanding contracts and working closely with the Corporate Business Development and our Companys Research & Development Division Alliance Management Teams

  • Assess GRACS Integration related problem situations to identify causes gather and process relevant information generate possible solutions make recommendations and/or resolve the problem and direct the resolution of complex business problems.

  • Ensure adherence to the established common network framework for GRACS functional areas to understand/evaluate business partner operations establish guidelines for working together and leverage differences to create value share best practices and deliver activities to drive knowledge transfer between GRACS team members. Provide training as necessary on successful partner relationship skills including process collaboration communication and tools.

  • Develop the functional alliance relationship to support effective business deal execution engage partners and GRACS applicable personnel to explore the potential challenges of working together examine differences develop shared protocols for managing those differences and establish mechanisms for their day-to-day work.

  • Work closely with the Mature Deals and Operations team to define establish and drive continuous improvement of the Business Process for the pre and post execution phases of Business Development Agreements with focus on how the different GRACS functions and business partners collaborate.

  • Specific to opportunities where an ongoing relationship is maintained with the business partner the incumbent will be responsible for serving as the point of contact for all alliance management issues related to ongoing GRACS activities.

  • The Director may also have people management responsibilities related to oversight of team members in supporting opportunities in a similar manner as described above. Additionally the incumbent will assume the responsibilities for employee development and management consistent with Company Leadership and Diversity and Inclusion principles.


Education:

  • BS Degree preferably in technical business or science.

Required Experience:

  • At least 12 years in the pharmaceutical industry with at least 5 years in Regulatory/Pharmacovigilance Function or Business Development.

  • Ability to influence and effectively operate in an ambiguous/rapidly changing environment while being quality and compliance oriented.

  • Proven and demonstrated skills in project management and leadership strategic proactive and a creative problem-solver that generates options and drive results in a deadline driven environment.

  • Strong virtual and in person collaboration

  • Demonstrated facilitation and leadership skills.

  • Clear communicator and goal oriented.

  • Comfort and experience building and presenting effective slide presentations with audiences at all levels of the organization.

  • Independent thinker and worker. Highly organized motivated and detail-oriented while still able to keep overall big picture view of projects and strategies.

  • Demonstrated analytical and data management skills. Experience pulling together abstract milestones and data into centralized management report.

  • Demonstrated ability to lead cross functional teams and facilitate cross functional meeting to achieve a purpose.

  • Strong demonstrated project management capabilities and skills. Ability to collaborate and manage multiple projects at various stages of the process simultaneously.

  • Ability to communicate messages in a clear and concise manner both verbally and in writing. Experience with change management concepts and execution.

  • Strong proficiency with generating content using all MS Office tools including but not limited to Word Excel Power-Point and SharePoint.

  • Some experience creating and modifying MS Teams and MS Project or related tools to manage project timelines and collaboration.

  • Ability to effectively work seamlessly with all levels of personnel.

  • Demonstrated sensitivity and knowledge of Diversity and Inclusion principles

Desired Experience:

  • Experience with Business Development and/or Regulatory strategy and process for partnerships (multiple deal or execution types) preferred.

  • Experience with partnerships contracts and agreements

  • Project Management Professional (PMP) Certification and/or Six Sigma Green or Black

Required Skills:

Accountability Accountability Biopharmaceutical Industry Business Processes Communication Cross-Functional Teamwork Decision Making Detail-Oriented Diversity and Inclusion (D&I) Divestitures Employee Training Programs EU Legislation In Licensing Mentorship Mergers and Acquisitions (M&A) Negotiation Out Licensing People Leadership Pharmaceutical Regulatory Affairs Pharmacovigilance Regulatory Affairs Compliance Regulatory Affairs Management Regulatory Compliance Regulatory Experience Regulatory Intelligence 4 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only:

Our company is committed to inclusion ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race color age religion sex sexual orientation gender identity national origin protected veteran status disability status or other applicable legally protected a federal contractor we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together talented and committed people with diverse experiences perspectives skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas broad experiences backgrounds and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anothers thinking and approach problems collectively.

Learn more about your rights including under California Colorado and other US State Acts

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

$169700.00 - $267200.00

This 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

Search Firm Representatives Please Read Carefully
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:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

10/31/2025

*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

Job DescriptionUnder the minimal guidance of the Senior Director Business Development Execution the incumbent manages and is responsible for the business process and related activities associated with Global Regulatory Affairs and Clinical Safety (GRACS) Business Development Execution. The primary f...
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Key Skills

  • Proofreading
  • Adobe Acrobat
  • FDA Regulations
  • Manufacturing & Controls
  • Biotechnology
  • Clinical Trials
  • Research & Development
  • GLP
  • cGMP
  • Product Development
  • Chemistry
  • Writing Skills

About Company

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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

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