Clinica Safety Scientist

hace 5 meses


Bogota, Colombia MSD A tiempo completo

**Job Description**:
Individual Case Medical Review (ICMR)

The Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. Assists the protocol lead in safety reporting activities for multiple clinical trials. The CSS may support collaboration with cross-functional colleagues within clinical development, clinical operations, case processing and medical safety review.

Key Responsibilities:

- Intake of reportable safety event information from clinical trial investigator sites
- Review, manage and create individual case safety reports for each event
- Ensure that all information required for a clinically complete and accurate case is present
- Generate safety queries to the trial investigator sites to ensure case report accuracy and completeness
- Prioritize daily work to ensure all events are submitted for entry into the safety database within the established timeframes
- May collaborate with cross-functional colleagues as needed

Qualifications & Skills
- Basic understanding of scientific and medical concepts
- Basic understanding of drug development
- Basic knowledge of GCP and ICH regulations98
- Ability to work as part of a cross-functional team
- Ability to identify and escalate problems and contribute to issue resolution
- Time management and organizational skills
- Strong communication skills with advanced oral and written English skills
- Advanced computer, database skills

Education Requirement:

- M.D. with minimum 1 year of clinical work experience in a patient care setting or 2 years relevant pharmaceutical, drug development, and/or drug safety experience.

Preferred:

- Experience in patient care setting, drug safety and pharmaceutical drug development

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Project Temps (Fixed Term)

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Requisition ID**:R251453



  • Bogota, Colombia MSD A tiempo completo

    **Individual Case Medical Review (ICMR)** The Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development. Assists the protocol lead in safety reporting activities for...

  • Drug Safety Scientist

    hace 7 meses


    Bogota, Colombia Merck A tiempo completo

    **The Position** - Supports the Global Pharmacovigilance and Safety Science (GPSS) team in the safety surveillance (e.g., signaling) and risk management (routine - as well as additional risk minimization measures, Risk Management Planning) of assigned, more complex established brands products and/or key new asset products (devices and/or medicinal...

  • Drug Safety Scientist

    hace 6 meses


    Bogota, Colombia Organon A tiempo completo

    **The Position** - High performing senior specialist who leads signal detection, safety evaluation and risk management planning and activities for key Organon’s _highly complex_ medicinal products and/or medical devices during clinical development and/or for post-marketing PV setting from a scientific perspective by active participation and contribution...

  • Drug Safety Lead

    hace 6 meses


    Bogota, Colombia Organon A tiempo completo

    **The Position** - Leads signal detection, safety evaluation and risk management planning and activities for low-medium complex_, _medicinal products and/or medical devices during clinical development and/or for established brands from a scientific perspective by active participation and contribution to, amongst others, the Organon Asset teams (when...

  • Safety Data Specialist

    hace 5 meses


    Bogota, Colombia MSD A tiempo completo

    **Job Description**: Como Safety Data Specialist, en Global Pharmacovigilance Case Management, eres responsable de procesar la información de eventos adversos, en el sistema de seguridad global para productos en investigación y/o comercializados, bajo la dirección y supervisión de un Gerente de Global Pharmacovigilance Case Management. El Safety Data...

  • Safety Data Specialist

    hace 2 semanas


    Bogota, Colombia MSD A tiempo completo

    **Job Description**:Como Safety Data Specialist, en Global Pharmacovigilance Case Management, eres responsable de procesar la información de eventos adversos, en el sistema de seguridad global para productos en investigación y/o comercializados, bajo la dirección y supervisión de un Gerente de Global Pharmacovigilance Case Management.El Safety Data...


  • Bogota, Colombia Novartis A tiempo completo

    **Summary**: Monitorea y audita el programa de vigilancia de medicamentos, productos biológicos o dispositivos médicos de la compañía, incluida la ingesta, evaluación, procesamiento y seguimiento de informes adversos. Participa en la resolución de cualquier responsabilidad legal y en el cumplimiento de la normativa gubernamental. Garantiza una...

  • Bacteriologo(a)

    hace 5 meses


    Bogota, Colombia Cenasit Safety sas A tiempo completo

    Requiere importante IPS de Salud Ocupacional en Bogotá Experiência de un año en laboratorio clínico, toma de muestras, procesamiento y cargue de resultados en historia clínica digital. Contrato por prestación de servicios, inicio inmediato. horario de lunes a sábado de 6: 00 am a 12 :00 pm salario 2.650.000 Tipo de puesto: Medio tiempo Sueldo: A...


  • Bogota, Colombia Air Products A tiempo completo

    At Air Products, our purpose is to bring people together to reimagine what’s possible, collaborate and innovate solutions to the world’s most significant energy and environmental sustainability challenges. Grow with us as we embark on building tomorrow together by being the safest, most diverse and most profitable industrial gas company in the...


  • Bogota, Colombia Takeda Pharmaceutical A tiempo completo

    **Therapeutic Area Lead Gastroenterology** - English version_ **WHAT YOU WILL DO** The Therapeutic Area Lead is responsible for providing overall, strategic and managerial leadership for Medical Affairs within a specific Therapeutic Area (Gastroenterology). The position will contribute to the achievement of business success by putting the patient’s needs...