Sr. Clinical Data Manager

MSD LATAM; Bogotá ciudad; Híbrido; COP 90.000.000 - 120.000.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Hybrid work arrangement

Professional development opportunities

Descripción de la vacante

MSD LATAM is seeking a Clinical Data Manager (SCDM) to lead end-to-end data management activities for clinical trials, including tool development, validation and maintenance, data integrity review, query management, and database lock preparation, in line with SOPs and ICH-GCP.

The ideal candidate will have a life sciences or related degree with relevant clinical data management experience, fluent English, and the ability to work in a fast-paced, hybrid environment supporting RBQM, AI-enabled

Formación

• Bachelor's or higher in life sciences, CS or related with ≥1 year clinical data management exp.
• Associates Degree with ≥2 years clinical data management exp.
• High School Diploma with ≥3 years clinical data management exp.

Responsabilidades

• Lead end-to-end data management activities for clinical trials.
• Perform data validation, data cleaning, and reconciliation.
• Manage data queries and database lock preparation/execution.
• Ensure compliance with SOPs and ICH-GCP; support RBQM/AI-enabled capabilities.

Conocimientos

Clinical Data Management

Data Validation

Regulatory Knowledge

RBQM

Communication

Educación

Bachelor's in Life Sciences/CS or related

Associates Degree in related field

High School Diploma with data management experience

Herramientas

EDC Software

Data Management Tools

Descripción del empleo

Job Description

Under the direction of the applicable management, the Clinical Data Manager (SCDM) is responsible for executing end-to‑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 organization’s ability to support RBQM, AI‑enabled capabilities, medical monitoring, site monitoring, and SDV‑related needs. In Early Stage Development (ESD), the SCDM may have sole responsibility for these activities; in Late Stage Development (LSD), the SCDM’s 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 self‑driven, with advanced expertise in work planning, prioritization, and time management.
• Fluent professional English, written and spoken, for global and cross‑functional collaboration.
• Strong end‑to‑end 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 fast‑paced, changing environments.
• Clear and effective communicator across technical, clinical, and business stakeholders.
• Demonstrated leadership and decision‑making contribution, with confidence to challenge and influence.
• Hands‑on expertise in Data Validation component design and development.
• Proven capability to translate protocol requirements into high‑quality 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}

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

09/30/2026

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

R417742