ThinkWell
ThinkWell
ThinkWell works with health systems to improve access to and quality of care, with a focus on universal health coverage. Its work spans health financing, governance, research and evaluation, and health workforce planning. The company helps public and private sector partners strengthen public financial management and use strategic purchasing to support primary healthcare. ThinkWell’s projects operate across multiple countries and are supported in part by grants, including funding from the Bill & Melinda Gates Foundation. The company’s work brings together policy, financing, and practical tools to address health system challenges.

Senior Health Regulatory Expert, Colombia

ThinkWell seeks a Colombia-based consultant to map health laws and regulatory reforms for a policy white paper. The work includes stakeholder interviews and assessment of legal pathways.

Aprašymas

  • Map Colombian laws, decrees, resolutions, and ongoing reforms relevant to the white paper, including Ley 2294 de 2023, the INVIMA reform bill, and the government’s deregulation agenda.
  • Interview and document discussions with officials at INVIMA, MinSalud, and other institutions, as well as health associations and gremios; conduct approximately 10 interviews over two rounds.
  • Evaluate the legal feasibility of proposed reforms and identify the appropriate legal instrument and approval route for each.
  • Check legal references and institutional responsibilities throughout the draft and final white paper.

Reikalavimai

  • Bring at least 10 years of experience in Colombian health law, regulation, or policy, with direct knowledge of INVIMA, MinSalud, and the legislative process.
  • Have established relationships with government officials and sector associations.
  • Be fluent in Spanish and have professional working proficiency in English.
  • Hold a law degree or an advanced degree in health policy or a related field.
  • Disclose any relationships with pharmaceutical, medical device, or insurance companies, EPS, or gremios.

Susiję darbai

Worldwide Clinical Trials

Senior Oncology Clinical Trial Manager – Europe (Remote)

Worldwide Clinical Trials

Lead oncology site management across Europe at Worldwide Clinical Trials, a global contract research organization. Oversee monitoring, regulatory compliance, recruitment, risk management, and study teams.

Atidaryti
Thermo Fisher Scientific

Senior Clinical Quality Assurance Compliance Manager

Thermo Fisher Scientific

Lead clinical quality assurance, risk management, and governance for Thermo Fisher Scientific’s clinical research business. Home-based position supporting clinical study teams across the United States.

Atidaryti