Job Information
Merck Senior Director, GMVC, Oncology MISP/Congress Operations (Hybrid) in North Wales, Pennsylvania
Job Description
Role Summary:
The Senior Director (SD), Oncology MISP (Investigator Studies Program)/Congress Operations, Value & Implementation (V&I) Global Medical and Value Capabilities (GMVC), leads a team of project management, or research management professionals to operationalize our company’s oncology portfolio of Investigator-Initiated Studies (IIS).
The SD Oncology MISP/Congress Operations is responsible for the efficient and compliant end-to-end execution of research activities from committee review and approval through budgeting, contracting, study execution to publication and closeout.
The SD Oncology MISP/Congress Operations oversees a multi-million-dollar budget supporting 900 predominately interventional IIS and interacts with 15 review committees.
The SD Oncology MISP/Congress Operations is responsible for supporting alliance activities for IIS activities including establishing governance, ways of working, and training.
The SD Oncology MISP/Congress Operations is responsible for effectively implementing GMVC and ourResearch & Development Division standard operating procedures across the relevant phases of IIS activities.
The SD Oncology MISP/Congress Operations partners with Congress Operations for major Oncology congresses providing PM support from the team to facilitate our Research & Development Division debriefs, abstract planning, and SL engagements.
Responsibilities and Primary Activities:
Key Functions
Manages operational support for IIS in collaboration with MISP Chairs (Executive Director of Scientific Affairs)
Ensures scientific, strategic and operational alignment across multiple tumor and asset teams
Optimizes MISP resources and study budgets to ensure linkage to strategic alignment with V&I Plans
Instills a culture of best practice and knowledge sharing and continuous improvement
Oversees coordination of clinical supply for IIS, partnering with Global Clinical Supplies (GCS) and our Company's Manufacturing Division
Partners with legal, compliance and other research operations functions
Monitors initiatives to ensure adequate resourcing and timely execution
Identifies overlapping initiatives and if needed, aligns/stops activities to ensure efficient use of resources
Oversees initiatives and communicates status to senior management on a regular basis
Ensures the efficient implementation of operational excellence and process improvement initiatives across the entire Oncology MISP portfolio
Assists in building and maintenance of the MISP research operating model and processes
Recruits and develops new team members into their assigned roles and responsibilities
Fosters sharing of relevant best practices across the enterprise
Critical Competencies/Key Functional Skills and Knowledge
Expertise and experience overseeing an operations team
Ability to develop talent throughout the organization
Ability to collaborate in cross-functional and cross-enterprise teams and working groups
Ability to lead in a matrix organization, including managing of direct and indirect reports and other functions without direct authority
Demonstrated skills working in complex corporate environments and exercising influence without positional authority
Demonstrated skills in identifying process gaps and building new processes
Demonstrated decision-making skills and effective communication skills
Demonstrated leadership in working with networks, experimentation, sharing information and learning from best practices
Strong strategic thinking, creating an organizational vision and empowering teams to achieve success
Strong interpersonal skills, communication, collaboration, and internal/external networking capabilities
Exhibits executive presence, deep subject matter expertise and strong business acumen
Required Qualifications , Skills & Experience:
Minimum :
Bachelor’s Degree in scientific, research, operational or business discipline
10+ years of leading, teams responsible for global research operational activities
Experience leading and directly managing teams, including leading cross-functional teams and managers of managers
Ability to navigate new or ambiguous situations
Experience initiating, developing and leading broad-scale process improvement projects and programs
Experience making complex decisions and strategic choices
Preferred :
Master’s Degree (business, operations, or scientific discipline)
Experience with the compliance landscape required for research, e.g. Good Clinical Practice (GCP), Good Manufacturing Practice (GMP) and Good Pharmacovigilance Practice (GPP)
Leading a diverse workforce and managing mix of full-time and contractor employees
Demonstrated ability to build, mentor and develop talent
Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)
Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
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 (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.
We are an Equal Opportunity Employer, committed to fostering an inclusive and diverse workplace. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or other applicable legally protected characteristics. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
EEOC Know Your Rights (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)
EEOC GINA Supplement
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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:
$164,800.00 - $259,400.00
Available 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 (https://www.benefitsatmerck.com/) .
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:
No relocation
VISA Sponsorship:
No
Travel Requirements:
10%
Flexible Work Arrangements:
Hybrid
Shift:
1st - Day
Valid Driving License:
No
Hazardous Material(s):
N/A
Job Posting End Date:
12/31/2024
*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.
Requisition ID: R326315