Job Details
Director, Global Professional Relations and Independent Medical Education Grant Operations Quality Team Leader
Job Description
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized. We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio.
Role Summary:
Under the direction of the Executive Director of Global Professional Relations and Independent Medical Education (gPRIME), the Director of gPRIME Grant Quality is primarily responsible for providing strategic leadership in defining the broad direction of the Teams Continuing Education/Continuing Professional Education (CE/CPE) and non-CE Grant Programs with planning, implementation, and oversight of quality activities for the gPRIME organization related to internal and external requirements, as well as for driving business ownership of quality and compliance within gPRIME. The role directs the planning, management, implementation, oversight (controls), and evaluation of extended functional teams and systems to improve the grant/funding process.
The Director liaises with local and regional CE providers, educational organizers, adult-learning experts, and professional medical societies, along with company personnel to assist and encourage timely and accurate grant proposal submissions aimed to improve the quality of healthcare.
The Director has overall responsibility for managing departmental transactions with emphasis on independent grant processing and tracking financial/compliance/internal and external policies.
Responsibilities and Primary Activities:
Quality Lead
Ensures full compliance with existing guidelines consistent with external regulatory bodies, company policies, and business principles
Partners with cross-functional teams to regularly review and lead development and update of gPRIME-related policies, guidance, standard operating procedures (SOPs), executional resources, and processes to ensure activities are planned and conducted in accordance with applicable laws, rules, and regulations
Partners with stakeholders across Business areas, Compliance, and Legal to improve and simplify policies, guidance, and processes to obtain quality and operational effectiveness
Participates in audit and monitoring planning with Audit and Compliance groups
Implements rigorous systems and process controls to ensure quality procedures and documentation
Interprets and makes principle-based decisions informing unique situations
Maintains high level of readiness to respond to internal audit, external inspection, eDiscovery requests, and our Research & Development Division and Human Health (HH) non-promotional compliance monitoring plan and implements remediation activities as necessary
Manages and resolves all quality issues, potential non-compliance, and deviations, including implementation of corrective and preventative actions as appropriate
Oversees the Headquarter Grant Management System for gPRIME including any necessary upgrades to process, reporting or the annual contract for this paid 3rd party system in partnership with our Research & Development Division Grant Operations as part of the Headquarter Governance Council
Process and Systems
Enables gPRIME strategic priorities by directing the end-to-end stewardship and advancement of process workflows powered by high-quality, integrated systems
Drives principle-based global processes and a quality systems mindset for key activities driving the awareness, understanding, buy-in, and support through change-management activities
Ensures coordination between the regions and functions to drive consistency in approach and implementation
Develops a process and systems strategy/roadmap and ensures effective prioritization and governance, managing the portfolio of work required to reduce operational inefficiency and risk utilizing process simplification
Manages implementations and steady-state operations related to processes and systems/technologies to enable business vision, anticipating future needs/capabilities and measuring performance to inform necessary improvements
Creates a culture of innovation and drives the execution of applicable transformational and innovative solutions
Builds solid working relations across and within cross-functional teams to ensure that all areas and supporting functions are well represented and are in alignment with the process and systems vision and roadmap
Sets Direction and Strategy
Builds and maintains the division’s strategic and tactical approaches to the CE/CPE, non-CE, and headquarter-based international independent medical education (IME) grant programs to ensure company support of high-quality medical education for healthcare professionals that complies with CE accrediting and government agency guidelines, as well as internal policies.
Negotiates profit plan and supplemental funding with GMSA Finance and effectively manages disease-state budgets
Creates and communicates a clear, shared vision for the future consistent with our Company's values and mission
Leads and promotes customer-focused strategies and ensures strategic initiatives are transformed into actionable business plans
Maintains a balanced perspective between short- and long-term priorities and manages the dynamic tension between un-realistic goals and realistic plans
Can adapt quickly to new situations and changes in the broader healthcare environment
Manages Business Complexity
Makes timely, insightful decisions based on the best information available and takes effective action, incorporating a balance between patient outcomes and reasonable risk
Establishes and ensures adherence to corporate guidelines and processes within and across functions and divisions while maintaining an entrepreneurial spirit
Plans for growth and expansion and acts as a catalyst for positive, constructive change
Drives Performance
Sets clear and challenging expectations and holds self and others accountable for meeting and/or exceeding them
Consistently delivers on commitments and develops and applies new and unique methods and thinking to executing plans and strategies
Continues to drive performance until objectives are met and does not back down in the face of adversity or obstacles to achieve the best results for patient care and business objectives
Collaborates Across Boundaries
Identifies and eliminates silo thinking, creates company-wide solutions, and builds long-term alliances with other departments, functions, or businesses to create action plans
Seeks multiple perspectives and engages in open and honest two-way communication to consider diverse points of view, and consistently develops and sustains cooperative working relationships
Develops People
Implements our Company's principles of high-performance teaming and can build best team and talents
Ensures the implementation of gPRIME onboarding process and meaningful discussion of people-development plans leading to setting up attracted talents for success and providing them with the best opportunity to grow
Provides regular and consistent leadership, guidance, and coaching to his/her team
Works with team to develop clear objectives and is responsible for following all Human Resource (HR) processes and ensuring completion within deadlines directed by HR and Global Human Health (GHH) management
Maintains a productive work environment and creates and sustains an environment where it is safe to speak up (measured through feedback from direct reports) and which embraces and understands cultural diversity and diversity of thought
Models the highest possible standards of ethics and integrity
Manages the application and communication of relevant policies, procedures, and our Company's Ways of Working
Oversees the team of our Company's FTEs and outsourced staff who manage and execute contracts and payments for all gPRIME programs
Required Qualifications, Skills, & Experience
Minimum Required Education:
BS/BA degree
5 years of demonstrated experience in a US and or global pharmaceutical-related role
Experience:
3 years of experience in operations and grant management systems
Demonstrated leadership and ability to collaborate with high-performing groups of technical professionals
Experience developing business strategies and managing multi-functional/cross-functional teams
Demonstrated leadership as agent for change and expertise and advice that other leaders, internally and externally, seek out
Advanced compliance IQ and experience working in a heavily regulated environment
Advanced knowledge and in-depth understanding of our Company’s compliance framework, including relevant policies and SOPs
Preferred
MBA
Entrepreneurial mindset, excellent organizational skills, sense of urgency when making decisions, and ability to communicate effectively to all constituencies both internally and externally
Negotiation skills with a keen ability to identify and communicate "win-win" solutions for all parties
We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.
Who we are …
We are known as Merck & Co., Inc., Kenilworth, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world's most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.
What we look for …
In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth.
Invent. Impact. Inspire.
NOTICE FOR INTERNAL APPLICANTS
In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
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We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.
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Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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:
Flexible Work Arrangements:
Shift:
Valid Driving License:
Hazardous Material(s):
Number of Openings:
1Requisition ID:R117788