Government Affairs - Bogotá, D.C, Brazil

The Head of Corporate Affairs will drive the implementation of the Tetra Pak Corporate Affairs strategy in the region to ensure a regulatory environment that supports and/or does not harm our business objectives. · ...

+Job summary · Patient Affairs and Public Affairs Manager responsible for patient advocacy, public affairs, communication, market access and corporate social responsibility.+Qualifications · Bachelor's degree in Communication or related field. 2-3 years' experience with patient a ...

The Head of Corporate Affairs will drive the implementation of the Tetra Pak Corporate Affairs strategy in Central America to ensure a regulatory environment that supports our business objectives. · Monitor and analyze relevant policy topics and files. · Manage a portfolio of rel ...

+The company is searching for a Director, Regulatory Policy to be in their Sao Paulo office. The job is responsible for shaping and advancing the company's regulatory policy agenda across global and regional platforms. · ...

The NOLA Cluster Medical Director provides leadership to all cross-cluster and in-country medical functions. The role includes providing scientific guidance across the Pfizer portfolio and embracing innovation. · The cluster medical director reports to EM LATAM Medical Lead and p ...

We are searching for the best talent for Director, Regulatory Policy - Latin America, to be in our São Paulo, Brazil; CDMX, Mexico; Buenos Aires, Argentina; Bogotá, Colombia or · Lima, Perú office..The Director, Regulatory Policy is a strategic leader responsible for shaping and ...

Provides specialist medical/scientific strategic and operational input for a cluster of countries within Central America and the Andean territories into core medical affairs activities such as: healthcare professional/provider interactions (Payers, Patients, Prescribers, and Prov ...

Title: · Patient Affairs and Public Affairs ManagerCompany: · Ipsen Colombia S.A.SAbout Ipsen: · Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly ...

We're looking for a talented Licensing & Regulatory Affairs Associate, to support our Compliance Team from our Bogotá office. · We believe in equal opportunity and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gende ...

The Regulatory Submission Integration specialist is responsible for the end-to-end transfer, · validation,and integration of regulatory submission documents and associated metadata from acquired companies into · the Veeva Regulatory Information Management (RIM) platform. · Docume ...

Sr Brand Manager High Specialty · Position Summary · The Senior Brand Manager is responsible for developing and executing strategic marketing plans for oncology and high specialty products, ensuring strong market positioning and sustainable growth. This role drives brand performa ...

Se busca experto/a en monitoreo y evaluación para apoyar al equipo de la Embajada canadiense en Colombia con el desarrollo del programa FSSP. · ...

+ Develop and execute fiscal policy agendas for Latin America · + Coordinate regional initiatives and track progress · + Analyze and translate complex regulatory topics into practical guidance · + Advise on global best practices related to tax policy and advocacy approaches ...

The Senior Internal Communications Analyst is responsible for planning, executing, and enhancing communication strategies that strengthen employee engagement, · organizational culture, · and the connection between employees and leadership.This role acts as a strategic partner to ...

At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. · ...

The Sr Manager, Strategic Value & Access, is accountable for leading and executing the market access, pricing, and reimbursement strategy across the product lifecycle, · This position ensures that company products achieve and maintain optimal access through robust value propositi ...

We are seeking a detail-oriented and people-focused Project Manager – Regulatory Operations to lead and support cross-functional initiatives within Regulatory Operations BU based in Bogota. · The Project Manager will plan, organize, assign, and balance the workload of the Regulat ...

This position works out of our Bogota in the division Established Pharmaceuticals.As the Global Medical Safety Expert – Biosimilars provide expert leadership direction and scientific guidance for pharmacovigilance activities within assigned area of responsibility. · ...

River Global offers a regulatory affairs consultant position to monitor and analyze regulatory frameworks in LATAM. · ...

+The Regulatory Submission Integration specialist is responsible for the end-to-end transfer, validation, and integration of regulatory submission documents and associated metadata from acquired companies into the Veeva Regulatory Information Management (RIM) platform. · + ...