Empleos actuales relacionados con Clinical Operation Manager - Bogotá, Bogotá D.E. - MSD

  • Medical Manager

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia Ipsen A tiempo completo

    Job SummaryWe are seeking a highly skilled Medical Manager to join our team at Ipsen. As a Medical Manager, you will play a critical role in providing scientific information and support to external stakeholders, including Health Care Professionals (HCPs) and Key Opinion Leaders (KOLs).Key ResponsibilitiesProvide Scientific Information and SupportRespond to...

  • Clinical Trials Regional Project Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia PSI A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Trials Regional Project Manager to join our team at PSI. As a key member of our Clinical Operations department, you will be responsible for coordinating project activities, ensuring milestones are met, and maintaining consistency of Clinical Operations processes across regions.Key ResponsibilitiesCoordinate...

  • Clinical Data Science Manager

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job DescriptionMSD is seeking a highly skilled Clinical Data Science Manager to join our team. As a key member of our organization, you will play a critical role in guiding our data management strategy and ensuring the highest standards of accuracy and efficiency in our clinical operations.Main Responsibilities:Develop and implement data management...

  • Clinical Research Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Manager to join our team at MSD. As a Clinical Research Manager, you will be responsible for the end-to-end performance and project management of assigned protocols in a country, ensuring compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards, and...

  • Clinical Data Science Manager

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    About the RoleWe are seeking a highly skilled Clinical Data Science Manager to join our team at MSD. As a key member of our organization, you will be responsible for leading our clinical data management efforts and ensuring the highest standards of accuracy and efficiency.Key ResponsibilitiesDevelop and implement strategic initiatives to improve data...

  • Clinical Research Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job DescriptionThis role is primarily accountable for the end-to-end performance and project management for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally.The CRM could be responsible for a particular...

  • Clinical Trials Regional Project Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia PSI A tiempo completo

    Job DescriptionJob Summary:We are seeking a highly skilled and experienced Clinical Trials Regional Project Lead to join our team at PSI. As a key member of our Clinical Operations department, you will be responsible for coordinating project activities, ensuring milestones are met, and maintaining consistency of Clinical Operations processes across...

  • Clinical Research Associate

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    {"title": "Clinical Research Associate", "content": "Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for coordinating all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, and...

  • Clinical Operations Manager

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

    Job SummaryThis role is accountable for ensuring the performance and compliance of assigned protocols in a country, adhering to ICH/GCP and country regulations, company policies, quality standards, and adverse event reporting requirements.Under the oversight of the Head Clinical Operations Managers, the person is responsible for executing and overseeing...

  • Clinical Data Science Program Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia ICON A tiempo completo

    About the RoleWe are seeking a highly skilled Clinical Data Science Program Manager to join our team at ICON. As a key member of our Full Service IOD Clinical Data Science team, you will be responsible for ensuring program and study level goals and objectives are consistently met to the highest standard of quality.Key ResponsibilitiesProgram Management:...

  • Clinical Data Science Program Manager

    hace 2 semanas

    Bogotá, Bogotá D.E., Colombia ICON Plc A tiempo completo

    About the RoleWe are seeking a highly skilled Clinical Data Science Program Manager to join our Full Service IOD Clinical Data Science team at ICON Plc. As a key member of our team, you will be responsible for ensuring program and study level goals and objectives are consistently met to the highest standard of quality.Key ResponsibilitiesProgram Management:...

  • Clinical Trials Operations Manager

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia IQVIA A tiempo completo

    Job OverviewAs a key member of the IQVIA team, the Centralized Monitoring Lead will provide leadership and guidance to the centralized monitoring team to ensure the successful delivery of clinical trials. This role will work closely with project and clinical leads to achieve project objectives, optimize speed, quality, and cost of delivery, and ensure...

  • Clinical Specialist

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia Boston Scientific Corporation A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Field Specialist to join our team at Boston Scientific Corporation. As a Clinical Field Specialist, you will provide clinical, technical, and educational support to assigned accounts at a Territory, Regional, National, or EMEA level.Key ResponsibilitiesProvide Clinical Support: Offer field/remote clinical...

  • Lead Clinical Monitoring Specialist

    hace 1 mes

    Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    Position Overview:The Senior Clinical Research Associate (Sr CRA) plays a pivotal role in overseeing and coordinating the clinical monitoring and site management processes. This position is essential in ensuring compliance with ICH GCP, FDA regulations, local laws, and internal standard operating procedures.Key Responsibilities:Conducts thorough site visits...

  • Clinical Research Associate

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for coordinating all aspects of the clinical monitoring and site management process.Key ResponsibilitiesMonitor investigator sites to ensure the accuracy and validity of CRF entries in...

  • Senior Clinical Research Associate

    hace 1 mes

    Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    Position Overview:The Senior Clinical Research Associate plays a pivotal role in overseeing and coordinating all facets of clinical monitoring and site management in compliance with ICH GCP, FDA regulations, local laws, and Thermo Fisher Scientific's standard operating procedures.Key Responsibilities:Conduct site visits to evaluate adherence to protocols and...

  • Clinical Specialist Urology

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia Boston Scientific Corporation A tiempo completo

    About the RoleBoston Scientific Corporation is seeking a highly skilled Clinical Specialist Urology to join our team. As a Field Clinical Specialist, you will provide clinical, technical, and educational support to assigned accounts in a Territory.Key ResponsibilitiesProvide Field/Remote Clinical Support: Support case coverage, basic troubleshooting,...

  • Experienced CRA for Clinical Trials

    hace 1 mes

    Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo

    Position Overview:The Senior Clinical Research Associate (Sr CRA) plays a pivotal role in overseeing and coordinating all facets of clinical monitoring and site management in compliance with industry standards and regulations.Key Responsibilities:Conduct site evaluations to ensure adherence to protocols and regulatory requirements.Maintain ongoing...

  • Clinical Support Specialist

    hace 3 semanas

    Bogotá, Bogotá D.E., Colombia Boston Scientific Corporation A tiempo completo

    About the RoleBoston Scientific Corporation is seeking a highly skilled Clinical Support Specialist to join our team. As a Clinical Support Specialist, you will play a critical role in providing field and remote clinical, technical, and educational support to assigned accounts at a territory level.Key ResponsibilitiesProvide Field and Remote Clinical...

  • Senior Payment Manager

    hace 3 días

    Bogotá, Bogotá D.E., Colombia BOG Fortrea Colombia Ltda. A tiempo completo

    Job Title: Senior Payment ManagerFortrea is seeking a highly skilled Senior Payment Manager to join our team. As a key member of our financial operations team, you will be responsible for overseeing the payment process for our clinical trials.Key Responsibilities:Supervise and manage a team of payment professionals to ensure timely and accurate payment...

Clinical Operation Manager

hace 4 meses

Bogotá, Bogotá D.E., Colombia MSD A tiempo completo

Job Description

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally.

Under the oversight of the Head COMs, the person is responsible for execution and oversight of clinical trial country submissions and approvals and to ensure Site Ready.

Responsibilities include, but are not limited to:

• Executes and oversees clinical trial country submissions and approvals for assigned protocols.

• Develops local language materials including local language Informed Consents and translations. Interacts with IRB/IEC and Regulatory Authority for assigned protocols.

• Manages country deliverables, timelines and results for assigned protocols to meet country commitments. Responsible for quality and compliance in assigned protocols in country.

• Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management. Enters and updates country information in clinical and finance systems.

• Ownership of local regulatory compliance. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.

• Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval related-interactions. Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.

• Contribute or lead initiatives and projects adding value to the business, as appropriate/required.

• Contributes strongly to COM team and other Country Operations roles knowledge by acting as process Subject Matter Expert (SME), sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.

• Contributes to COM team knowledge by acting as buddy/mentor and sharing best practices as appropriate/require

Profile:

3 to 5 years of experience working with clinical studies at CROs or Pharma Industry

Strong Knowledge in regulatory relate with clinical studies.

English Business Proficency

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:

Project Temps (Fixed Term)

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):

N/A

Job Posting End Date:

06/23/2024

*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.

Job Posting End Date:06/23/2024

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:R298072