Associate Specialist, Clinical Data Management

MSD; Pennsylvania; Hybrid; USD 72,000 - 113,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Comprehensive benefits

Job summary

MSD in the United States is seeking an Associate Specialist, Clinical Data Management to execute end-to-end data management activities for clinical trials, including data capture, reconciliation, QA, and database lock preparation, in line with SOPs and ICH-GCP.

The role requires strong English communication, attention to data integrity, and collaboration with cross-functional teams across West Point PA and Rahway NJ under hybrid work arrangements.

Qualifications

• High School Diploma or equivalent.
• Preferred: B.A./B.S. in Medicine, Pharmacy, Nursing, Biological Sciences or related field.
• Fluent written and spoken English; ability to work in a regulated environment.

Responsibilities

• Execute end-to-end data management activities for clinical trials.
• Develop/change testable data management tools and systems.
• Run data integrity checks and manage query resolution with sites.
• Support validation, testing, and database lock preparation.
• Ensure compliance with SOPs and ICH-GCP throughout the study lifecycle.

Skills

Adaptability

Analytical problem solving

Clinical Data Cleaning

Clinical Data Management

Data Collection Methods

Data Documentation

Data Integrity

Data Processing

Data Reporting

Data Review

Data Validation

Document Management

Good Clinical Practice (GCP)

Project Management

Teamwork

Education

High School Diploma

Bachelor's degree (preferred)

Job description

## Associate Specialist, Clinical Data ManagementApply: Hybrid: USA - Pennsylvania - West Point: USA - New Jersey - Rahway: Full time: Posted Yesterday: End Date: October 29, 2026 (5 days left to apply): R422760**Job Description****Position Overview:**Under the direction of the applicable management, the Clinical Data Manager (CDM) is responsible for executing end to end data management activities pertaining to clinical trials, including but not limited to; data management tool and system development, validation and maintenance, data collection, data integrity review and reconciliation, query management, medical coding, and database lock preparation, in compliance with our Company's Standard Operating Procedures (SOPs) and ICH-GCP guidelines. **Primary activities include, but are not limited to:*** Participates in the development and change request implementation of data management tools and systems for the clinical trial data management activities under the direction of the SCDM/LCDM* Runs data integrity check reports in accordance with data review plans and relevant SOPs.* Raises questions to investigational site staff and internal and external vendors, reviews responses and corresponding data corrections to confirm identified issue resolution.* Responsible for the execution of user acceptance testing of data management tools under the guidance of the SCDM/LCDM.* Escalates overdue items, including but not limited to outstanding questions and missing visits.* Assists the Senior/Lead CDM with data management activities to resolve all identified data issues prior to study database lock.* Complete trial level archiving activities under the direction of the SCDM/LCDM including, but not limited to, filing of essential documentation.* Maintains compliance with standard key performance indicators according to process expectations at the protocol level.* Monitors data quality and cycle-time performance measures to maintain compliance, performs root cause analysis and implements action plans as needed.* Proactively communicates with Senior/Lead CDM to share project status, risk assessment and outstanding item resolution status. **Education Requirement:*** High School Diploma (or equivalent).* Preferred: B.A. or B.S. degree, in Medicine, Pharmacy, Nursing, Biological Sciences, or health care related discipline. **Knowledge and Skills:*** Self-motivated, excellent in work planning and time management.* Fluent oral and written English skills.* Good sense and awareness of regulations and policies.* Able to work under pressure and in a changing environment with flexibility.* Good communication skills with the ability to communicate with both the technical and business areas. #MSJR**Required Skills:**Adaptability, Analytical Problem Solving, Clinical Data Cleaning, Clinical Data Management, Data Collection Methods, Data Documentation, Data Integrity, Data Processing, Data Reporting, Data Review, Data Validation, Document Management, Good Clinical Practice (GCP), Project Management, Teamwork**Preferred Skills:**Current Employees apply HERECurrent 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 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 RightsEEOC GINA SupplementWe 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 primary location for this posting is:USA - Pennsylvania - West Point Where required by law, the compensation range for this role is provided below. The salary range for the primary location of this role is:$71,900.00 - $113,200.00 This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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. **Additional location(s):** Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location. **Additional location(s) Compensation Information:****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:**No Travel Required**Flexible Work Arrangements:**Hybrid**Shift:**1st - Day**Valid Driving License:**No**Hazardous Material(s):**n/a**Job Posting End Date:**10/29/2026**\\*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.**