Assoc. Director - Programmer (AI & Automation) (Hybrid)

Job Description

We aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. Join our team and contribute to our mission of using the power of leading-edge science to save and improve lives around the world.

Responsibilities

Oversee and coordinate clinical database activities across multiple clinical programs, including review of eCRFs, edit check specifications, and database development

Ensure adherence to clinical database standards, SOPs, and process guidelines

Plan and manage timelines for database deliverables; identify and escalate risks appropriately

Interface with study teams and stakeholders to integrate requirements into deliverables

Align with CDS leadership to ensure consistency of technical strategies and execution

Lead and participate in improvement initiatives, including task forces, automations, and exploration of emerging digital capabilities (e.g., advanced analytics, AI-enabled tools)

Contribute strategies and innovative solutions to enhance processes and increase productivity, including the appropriate use of automation and data-driven approaches

Support testing and evaluation of new systems, tools, and capabilities

Coordinate and contribute to CDS technical initiatives that improve efficiency and scalability

Serve as subject matter expert (SME) in clinical database and EDC activities, including database development and data integration

Increase functional effectiveness by supporting efforts to simplify and standardize processes, including identifying opportunities for automation and improved data workflows

Provide technical guidance, best practices, and knowledge sharing across the team and broader organization

Provide oversight and guidance to Clinical Database Developers

Support recruitment, onboarding, mentoring, and technical development of team members

Contribute to performance management input and capability development planning

Lead or contribute to functional and cross-functional meetings

Communicate clinical database processes, requirements, and risks effectively to stakeholders and vendors

Support alignment, decision-making, and continuous improvement efforts

Qualifications

Required

Bachelor’s degree in Computer Science or related discipline (or equivalent experience)

Minimum of 5 years of experience in pharmaceutical clinical research / data management

Experience in clinical database development, EDC systems, and data management processes

Strong understanding of clinical database design, eCRFs, edit checks, and data collection frameworks

Knowledge of EDC and data management systems

Familiarity with clinical data standards, regulatory requirements, and GxP/ICH guidelines

Understanding of end-to-end clinical data lifecycle and data cleaning processes

Strong stakeholder management and cross-functional collaboration skills

Effective communication and ability to translate technical concepts clearly

Strong organizational, prioritization, and multi-project management skills

Ability to work independently and manage competing priorities

High attention to detail and commitment to quality and compliance

Preferred

Experience in technology implementation and/or system evaluation

Exposure to automation tools, data workflows, and process optimization approaches

Demonstrated awareness of emerging digital capabilities, including automation and AI, and their potential application within clinical data management

Ability to identify opportunities to improve processes using data-driven and automation approaches, while ensuring compliance within regulated environments

Required Skills:

Adaptability, Adaptability, Artificial Intelligence (AI), Automation, Clinical Database Programming, Clinical Data Management, Clinical Data Standards, Clinical Development, Clinical Trials Operations, Data Analysis, Data Engineering, Data Quality Assurance, Data Reporting, Data Validation, Detail-Oriented, Drug Discovery Process, Escalation Management, FDA Regulations, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), Integration Architecture, Interpersonal Relationships, Mentoring Staff, Project Management Tools, Release Management {+ 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.

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

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.

You can apply for this role through https://jobs.merck.com/us/en (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:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Hybrid

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

06/20/2026*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: R399669