Associate Director, Clinical Data Management

Merck; West Point (PA); On-site; USD 142,000 - 224,000; Full time

Job summary

Merck is seeking a Principal Trial Manager to lead the data management strategy across one or more drug or vaccine trials and to oversee cross-functional initiatives within GDMS. You will provide SME-level guidance, mentor Trial Managers, and drive end-to-end data management proficiency across the department.

The role requires end-to-end data management knowledge, strong PM leadership, and the ability to work independently or as part of a cross-functional team with broad impact on quality and

Qualifications

• BA/BS degree in life sciences, computer science, or related discipline, with at least 6 years’ experience in Clinical Data Management or a mix between Data Management and Clinical Research and at least 3 years’ experience working with formal project management tools and processes.

Responsibilities

• Lead Special Projects and Initiatives within GDMS.
• Act as a SME, mentor, and trainer on data management, project management, leadership and other areas of expertise.
• Support Training & Development programs to promote Trial Manager end-to-end proficiency.
• Support and provide input to the functional process owners (PO)/ potentially serving as an SME to support process implementation.
• Partner with functional area representatives to assess and promote consistency in the use of database standards and trial design/peer review support as needed.
• Identifies, defines and implements improvements to data collection, data and project management processes and tools.
• Support audits and inspections as necessary.
• Functional & cross-functional special project management.
• Complex Risk Management.
• All required activities outlined in the TM job description.

Skills

Coordinate

Clinical Data Management

Clinical Data Standards

Data Management

Detail-Oriented

GCP

Influencing Skills

Mentoring Staff

Project Management Leadership

Strategic Thinking

Education

B.A./B.S. in life sciences or related

Tools

Job description

Job Description

The Principal Trial Manager is responsible for leading projects and initiatives to improve the quality and compliance of the data management functional areas in addition to the regular responsibilities as an individual Trial Manager.

The Principal Trial Manager is responsible and accountable for the successful execution of the clinical data management strategy for one or more drug or vaccine trials within the TM role. Will be responsible for leading and/or representing data management functional areas or GDMS in cross-functional initiatives and project teams as deemed appropriate.

Principle Trial Managers will possess end-to-end data management knowledge with strong project management and leadership skills which are transferable from pipeline to process to special initiatives. Will interact with Trial Managers as SME, Mentor and Trainer within areas of expertise and provide project leadership to help develop knowledge within the department and will be able to work independently or as a team member or leader with equal effectiveness.

Primary activities include, but are not limited to:

• Lead Special Projects and Initiatives within GDMS.


• Act as a SME, mentor, and trainer on data management, project management, leadership and other areas of expertise.


• Support Training & Development programs to promote Trial Manager end-to-end proficiency.


• Support and provide input to the functional process owners (PO)/ potentially serving as an SME to support process implementation.


• Partner with functional area representatives to assess and promote consistency in the use of database standards and trial design/peer review support as needed.


• Identifies, defines and implements improvements to data collection, data and project management processes and tools.


• Support audits and inspections as necessary.


• Functional & cross-functional special project management.


• Complex Risk Management.


• All required activities outlined in the TM job description.

Education/Experience (ex-Us, subject to local requirements):

• B.A. or B.S. degree, preferably in life sciences, computer science, or related discipline, with at least 6 years’ experience in Clinical Data Management or a mix between Data Management and Clinical Research and at least 3 years’ experience working with formal project management tools and processes.

Knowledge and Skills:

• Demonstrated accomplishments through all phases of the Study Life Cycle.


• Proficient overall working knowledge on the clinical development process.


• Knowledge of applicable regulations and policies.


• Be able to work under pressure in a changing environment with flexibility.


• Ability to work independently and accept and act with appropriate accountability with minimal guidance by management.


• Ability to coordinate the work of others and drive decision making.


• Exceptional communication skills (oral and written) with the ability to communicate with both the technical and business areas.


• Exceptional demonstrated organizational, problem-solving and negotiating skills.


• Demonstrated excellent project management and leadership skills.


• Demonstrated ability to coach and mentor others.


• Demonstrated ability to lead a cross functional Initiative with broad impact to Quality and Compliance.

clinicaltrialjobs

EligibleforERP

#GDMS

Required Skills:

Ability to Coordinate, Clinical Data Management, Clinical Data Standards, Data Management, Detail-Oriented, Good Clinical Practice (GCP), Influencing Skills, Mentoring Staff, Project Management Leadership, Strategic Thinking

Preferred Skills:

Cross-Functional Teamwork, Decision Making, Deliverables Management, Leadership, Leading Project Teams

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.

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 characteristics. As 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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088_EEOC_KnowYourRights_10_20.pdf)

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 another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/)

The salary range for this role is

$142,400.00 - $224,100.00

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 employee’s 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 https://jobs.merck.com/us/en/compensation-and-benefits .

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

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

No

Job Posting End Date:

08/28/2026

***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:

R413072