Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Job Description The Senior Scientist, Clinical Safety Scientist (CSS) supports safety reporting for clinical trials across multiple therapeutic areas and investigational product development programs, from early- through …
Skills: Drug Safety, Clinical Trials, Pharmacovigilance, Good Clinical Practice (GCP), Clinical Development
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to p…
Skills: Product marketing, Market development, Therapy adoption, Coronary interventions, Structural heart procedures
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Account Manager Market Access Location: Bogotá, Colombia About the job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work…
Skills: Market access, Stakeholder management, Project management, Content development, Communication
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Account Manager US Location: Bogotá, Colombia About the job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Bui…
Skills: Project management, Content lifecycle management, Stakeholder management, Scientific content development, Medical content development
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Vive la experiencia SONDA ¡Aquí transformas tu carrera! ¿Por qué ser parte de SONDA? Porque al igual que tú, amamos lo que hacemos, tenemos pasión por la innovación y estamos convencidos de que a través del conocimiento …
Skills: Requirements Gathering, Functional Analysis, Business Rules, User Stories, Traceability Matrices
Bogota, Capital District, RAP (Especial) Central, Colombia · Remote OK
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to p…
Skills: People Leadership, Inventory Management, Supply Chain Management, Order Fulfillment, Data Analysis
Bogota, Capital District, RAP (Especial) Central, Colombia · On-site
Help Bring Innovative Therapies to Patients Faster At IQVIA, we are dedicated to advancing healthcare through clinical research, technology, and data-driven insights. Every study we support contributes to the development…
Skills: Regulatory Affairs, Study Start-Up, Site Activation, Ethics Committee Submissions, Informed Consent Forms
AbbottBogota, Capital District, RAP (Especial) Central, Colombia · On-site
JOB DESCRIPTION: Pipeline Especialista de Control Financiero Acerca de Abbott: Abbott es líder mundial en cuidado de la salud, que crea ciencia innovadora para mejorar la salud de las personas. Siempre estamos mirando ha…
Skills: Financial Control, Sales and Cost Reporting, Gross Margin Forecasting, P&L Analysis, Expense Projection
Bogota, Capital District, RAP (Especial) Central, Colombia · Remote Solely
Colure Health operates the Mozaiq Care+ platform, which includes post-discharge outreach and ongoing care-management programs — Transitional Care Management (TCM), Chronic Care Management (CCM), Remote Patient Monitoring…
Skills: Bilingual Spanish and English, Patient Enrollment, Insurance Verification, Patient Outreach, Active Listening
Bogota, Capital District, RAP (Especial) Central, Colombia · Remote Solely
ABOUT COLURE HEALTH & THE ROLE Colure Health operates the Mozaiq Care+ platform and runs post-discharge care-continuity outreach for patients discharged from NYC Health + Hospitals facilities. The goal is simple: close t…
Skills: Bilingual Spanish and English, Patient Scheduling, Active Listening, Empathy, De-escalation
Bogota, Capital District, RAP (Especial) Central, Colombia · On-site
THE JOB AT A GLANCE This position is responsible for the completion of all tasks and duties required of a Medical Biller. These administrative and billing tasks are vital in ensuring our patients are billed accurately. T…
Skills: Medical Billing, Claim Processing, Revenue Cycle Management, Denial & Rejection Handling, Google Suite
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Career CategoryValue and AccessJob Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with s…
Skills: Market Access, Value Proposition Development, Key Account Management, Pharmacoeconomics, Health Technology Assessment
Bogota, Capital District, RAP (Especial) Central, Colombia · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Job Description Global Study Lead – This position is a fully client-embedded role, dedicated to a leading bio-pharma company. Role Purpose:…
Skills: Clinical Study Management, Vendor Management, CRO Oversight, Budget Management, Risk Management
Bogota, Capital District, RAP (Especial) Central, Colombia · Remote OK
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Project Manager - Make an Impact at the Forefront of Innovation The Project Manager serves as the Project Lead and primary spo…
Skills: Project Management, Financial Stewardship, Risk Identification, Issue Resolution, Cross-functional Team Leadership
Bogota, Capital District, RAP (Especial) Central, Colombia · On-site
The CPFR Specialist will act as a critical link between Opella, internal cross-functional teams, and Partner Markets distributors, driving Collaborative Planning, Forecasting and Replenishment practices to improve foreca…
Skills: Demand Planning, Supply Planning, CPFR, IBP/S&OP, Distributor Management
AbbottBogota, Capital District, RAP (Especial) Central, Colombia · On-site
JOB DESCRIPTION: Application ArchitectAt Abbott, we promote equal opportunity. We encourage persons with disabilities to apply, ensuring an inclusive and accessible recruitment process. Applicants must have a valid disab…
Skills: Cloud Architecture, Data Platform Design, AWS, Azure, Databricks
Bogota, Capital District, RAP (Especial) Central, Colombia · On-site
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Beckman Coulter Diagnostics, one of Danaher’s 15+ operating companies, our…
Skills: Commercial Management, Channel Partner Management, Strategic Planning, P&L Management, Business Development
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Company: Description: Estamos buscando una persona talentosa para unirse a nuestro equipo de Insurance Operations – Siniestros en Marsh. Este rol estará basado en Bogotá. Es un rol híbrido que requiere trabajar al menos …
Skills: Claims Management, Health Insurance Operations, Document Validation, Jira, MS Office
AbbottBogota, Capital District, RAP (Especial) Central, Colombia · On-site
JOB DESCRIPTION:Business Systems SpecialistAt Abbott, we promote equal opportunity. We encourage persons with disabilities to apply, ensuring an inclusive and accessible recruitment process. Applicants must have a valid …
Skills: Vaisala EMS Administration, IT Systems Support, Business Analysis, Incident Resolution, User Access Management
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Revenue and Receivables Manager Location: Bogotá About the job Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. …
Skills: Accounts Receivable, Revenue Recognition, SAP FI, MS Excel, Financial Reporting
Bogota, Capital District, RAP (Especial) Central, Colombia • Hybrid
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The Senior Scientist supports safety reporting for clinical trials by managing individual safety events and ensuring clinical data accuracy. They act as a protocol lead to collaborate with cross-functional teams and oversee safety queries throughout the drug development process.
Candidates must hold a Bachelor's degree in Medicine and possess at least 2 years of relevant professional experience in clinical practice or the pharmaceutical industry. Proficiency in English at a C1 level and knowledge of GCP and ICH regulations are required.
Job Description
The Senior Scientist, Clinical Safety Scientist (CSS) supports safety reporting for clinical trials across multiple therapeutic areas and investigational product development programs, from early- through late-stage development. This includes in-house trials and may include support for outsourced trials from integrations. The CSS collaborates with cross-functional colleagues in clinical development, clinical operations, case processing, and medical safety review.
Key Responsibilities:
Intake, review and management of individual reportable safety events from clinical trial investigator sites.
Ensure that all information required for a clinically complete and accurate case is present.
Develop clinically focused safety queries for trial investigator sites to support accurate and complete case reports.
Prioritize daily work to ensure all events are submitted for entry into the safety database within the established timeframes.
Complete protocol specific activities as required.
Maintain Protocol Specific Training (PST) requirements for assigned trials, including new amendments, to ensure protocol knowledge and understanding of their impact on safety reporting.
Actively participate and ensure effective communication with other team members supporting their protocols.
Appropriately escalate protocol or individual event issues with other stakeholders including CRAs/CRMs/CS/CD
May lead one or more protocols (as a protocol lead)
Triage safety queries from the clinical team and medical safety review team (ICMR-MSR) as applicable.
As a protocol lead participate as a core member of the Medical Monitoring Team
As a protocol lead participate and collaborate with the Clinical Trial Team
As a protocol lead reconcile critical data points between clinical and safety database as required.
Collaborate closely with cross functional colleagues.
Collaborate with external colleagues and business partners.
May serve as an expert resource for less experienced colleagues.
May provide training /oversight for new employees.
May participate in cross-functional or internal initiatives and/or process improvement projects.
May provide support to outsourced trials.
May serve as a Business Support team Leader.
Education Requirement:
Bachelor's degree in Medicine
Advanced English proficiency (C1 level). Proof of proficiency may be required.
Work Experience:
Minimum of 2 years of relevant professional experience in clinical practice and/or the pharmaceutical industry, including drug safety, clinical trials, drug development, with at least 1 year of clinical experience in a patient care setting.
Qualifications & Skills
Strong understanding of scientific and medical concepts.
Basic understanding of drug development.
Knowledge of GCP and ICH regulations.
Ability to work as part of a cross-functional team.
Effective decision making and independent problem-solving skills.
Time management and organizational skills.
Strong communication skills with advanced oral and written English skills.
Advanced computer, database skills.
Able to work under pressure, strong sense of responsibility and accountability.
Please submit your CV in English
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.
Travel Requirements:
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.
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
There are currently 247 open healthcare positions in Bogota, Capital District, Colombia listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Abbott, Johnson & Johnson Innovative Medicine, Medtronic, Sanofi, Air Liquide, among others. Browse the listings above to see every active employer.
Yes — 111 of the 247 open healthcare positions offer remote or hybrid work (32 remote, 79 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
