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Clinical Data Management Sr. Specialist

MSD


Job Location:

Bogotá - Colombia

Monthly Salary: Not provided by the employer
Posted: 17 September 2026 (12 hours ago)
Application Deadline: 15 December 2026
Vacancies: 1 Vacancy

Job Summary

Job Description

Under the direction of the applicable management the Senior Clinical Data Manager (SCDM) 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 integrity review and reconciliation query management and database lock preparation/execution in compliance with Company Standard Operating Procedures (SOPs) and ICH-GCP guidelines. The role also looks for candidates with relevant experience in adjacent clinical monitoring operational or technology areas particularly where such experience strengthens the organizations ability to support RBQM AI-enabled capabilities medical monitoring site monitoring and SDV-related Early Stage Development (ESD) the SCDM may have sole responsibility for these activities; in Late Stage Development (LSD) the SCDMs execution of these activities may be overseen by a Lead Clinical Data Manager (LCDM) or other manager.
Education and Experience:
At least B.A. or B.S. degree preferably in life science computer science or health care related discipline with at least 1 year professional experience in clinical data management;
OR
Associates Degree with at least 2 years professional experience in clinical data management;
OR
High School Diploma (or equivalent) with at least 3 years professional experience in clinical data management.
Preferable knowledge and skills:
  • Highly selfdriven with advanced expertise in work planning prioritization and time management.
  • Fluent professional English written and spoken for global and crossfunctional collaboration.
  • Strong endtoend understanding of the clinical development lifecycle.
  • Advanced knowledge of clinical practice and precise use of medical terminology.
  • Solid command of regulatory frameworks SOPs and compliance requirements.
  • Proven ability to perform under pressure in fastpaced changing environments.
  • Clear and effective communicator across technical clinical and business stakeholders.
  • Demonstrated leadership and decisionmaking contribution with confidence to challenge and influence.
  • Handson expertise in Data Validation component design and development.
  • Proven capability to translate protocol requirements into highquality Data Management specifications.
AND for External Candidates
  • Relevant experience in adjacent clinical monitoring operational or technology roles such as CRA CSSM or IT.
  • Working knowledge of RBQM AI-enabled capabilities medical monitoring site monitoring and SDV.
  • Ability to apply cross-functional experience to strengthen data quality risk oversight and stakeholder collaboration.
  • -Fluent oral and written English skills.

Required Skills:

Adaptability Adaptability Clinical Analytics Clinical Data Cleaning Clinical Data Management Clinical Development Clinical Reporting Clinical Research Communication Competency Management Customer-Focused Data Analysis Database Development Data Management Data Processing Data Quality Assurance Data Review Data Standards Data Validation Data Visualization Decision Making Early Phase Clinical Trials Electronic Data Capture (EDC) Learning Agility Pharmacovigilance 8 more

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

NA

Job Posting End Date:

09/29/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Senior IC


About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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