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Tecnimede Group

Clinical Pharmacologist

Tecnimede Group
Portugal · Full-time · Not Applicable

About the Position


The Tecnimede Group has 750 employees spread across the globe, looking toward the future, united and focused on improving and preserving the health of all of us. We oversee the entire life cycle of human-use medications, with our own factories located in Portugal and Morocco, and a Research and Development center in Torres Vedras (Portugal). We are 100% Portuguese, but also international, with a direct presence in over 100 countries. We are looking for people with strength, determination, and vision.


We are seeking to strengthen our team with a Clinical Pharmacologist, whose mission will be to contribute to the design, planning, and development of Clinical and Pre-Clinical Development Programs for value-added medications.


Responsibilities:

- Design, planning, and development of Clinical and Pre-Clinical Development Programs for value-added medications;

- Identification of the state-of-the-art regarding the epidemiological profile and treatment of diseases addressed by GTM medications;

- Drafting or reviewing clinical trial protocols that are integral parts of the Clinical and Pre-Clinical Development Programs;

- Assessment of the benefit/risk ratio of innovative medications and consideration of their added value (application of pharmacoeconomic concepts);

- Design, planning, and development of observational study protocols, both for efficacy and safety;

- Theoretical knowledge and practical application of guidelines for the R&D of new treatments (guidelines from EMA, FDA, ANVISA, among others);

- Preparation of scientific advice requests to competent authorities (competent authorities of the European Union; European Agency, ANVISA, FDA).


Requirements:

- Degree in Medicine with a specialization in Clinical Pharmacology or a related field;

- Demonstrable experience in clinical research and drug design;

- Excellent knowledge of pharmacology and pharmacodynamics;

- Strong problem-solving and analytical skills;

- Ability to work collaboratively with diverse teams;

- Ability to manage development projects from conception to the preparation of final reports.


Data Protection:

In compliance with the provisions of the GDPR and other applicable legislation on personal data protection, the hiring company guarantees that the processing of your personal data is lawful, fair, transparent, and limited to the purposes for which your data was collected.

Key Skills

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Posted
Nov 04, 2025
Type
Full-time
Level
Not Applicable
Location
Sintra

Industries

Pharmaceutical Manufacturing

Categories

Other

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