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(Associate) Medical Director - Dermatology, EMEA

Thermo Fisher Scientific

(Associate) Medical Director - Dermatology, EMEA

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Discover Impactful Work:

The (Associate) Medical Director will provide medical support and medical advice for Dermatology clinical trials and safety evaluation within the PPD Pharmacovigilance department.

A day in the Life:

  • Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials

  • Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead

  • During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions’ dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries

  • Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications

  • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP

  • Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties

Education

  • Medical Doctor, with a specialty in Dermatology

Knowledge, Skills, Abilities

  • Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important

  • Previous experience in a hospital setting

  • Is fluent in spoken and written English

  • Shown understanding and experience with NDA submission process.

  • Shown understanding of regulatory guidelines for adverse event reporting

  • Strong communication & presentation skills and is a strong teammate

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Locations

  • Remote, Portugal (Remote)

Salary

Estimated Salary Rangemedium confidence

40,000 - 65,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Medical leadershipintermediate
  • Protocol developmentintermediate
  • Medical monitoringintermediate
  • Stakeholder communicationintermediate
  • Compliance managementintermediate

Responsibilities

  • Provide medical support for Dermatology trials
  • Create clinical trial protocols
  • Real-time medical monitoring
  • Serve as medical point of contact
  • Interact with investigators/IRBs/Health Authorities
  • Ensure study compliance

Benefits

  • general: Meaningful work with global impact
  • general: Resources for career goals

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Thermo Fisher Scientific logo

(Associate) Medical Director - Dermatology, EMEA

Thermo Fisher Scientific

(Associate) Medical Director - Dermatology, EMEA

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Discover Impactful Work:

The (Associate) Medical Director will provide medical support and medical advice for Dermatology clinical trials and safety evaluation within the PPD Pharmacovigilance department.

A day in the Life:

  • Provide medical leadership to the study teams, including creating clinical trial protocols while implementing the latest scientific information, contribute to site selection, involved in review and approval of study protocols and amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), protocol deviation decisions and other clinical documents as required for the conduct of clinical trials

  • Real time Medical Monitoring of clinical studies: ensure medical validity of each individual primary endpoint as well study subject safety, while ensuring medical issues are identified early. Pro-active customer concern and correction of issues in consultation with the Global Medical Indication Lead

  • During initial review of protocol, consults with internal groups and support staff regarding procedural and budgetary items and the necessity for change due to any subsequent protocol amendments. Acquires other functions’ dedication to close gaps and address issues timely and effectively. Serves as chief liaison between sponsor and all PPD internal departments performing the required tasks during all study phases. Educates Investigator sites by delivering a protocol specific lab procedures presentation and demonstration during an investigator meeting. Controls, handles and follows day to day activities during the course of the clinical trial to resolve any issues and answer queries

  • Medical point of contact for all internal and external stakeholders: Interact with the investigators as needed, answer questions of IRBs and Health Authorities, prepare and present material to the study executive and independent safety committee if applicable; medical training of site staff at Investigator meetings; CRA training in new indications

  • Ensure study compliance for all medical aspects by understanding and applying all relevant SOPs and GCP

  • Closely collaborate with the cross functional study team members in order for medical risks, issues, and results to be clear to all involved parties

Education

  • Medical Doctor, with a specialty in Dermatology

Knowledge, Skills, Abilities

  • Significant experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important

  • Previous experience in a hospital setting

  • Is fluent in spoken and written English

  • Shown understanding and experience with NDA submission process.

  • Shown understanding of regulatory guidelines for adverse event reporting

  • Strong communication & presentation skills and is a strong teammate

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Locations

  • Remote, Portugal (Remote)

Salary

Estimated Salary Rangemedium confidence

40,000 - 65,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Medical leadershipintermediate
  • Protocol developmentintermediate
  • Medical monitoringintermediate
  • Stakeholder communicationintermediate
  • Compliance managementintermediate

Responsibilities

  • Provide medical support for Dermatology trials
  • Create clinical trial protocols
  • Real-time medical monitoring
  • Serve as medical point of contact
  • Interact with investigators/IRBs/Health Authorities
  • Ensure study compliance

Benefits

  • general: Meaningful work with global impact
  • general: Resources for career goals

Target Your Resume for "(Associate) Medical Director - Dermatology, EMEA" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for (Associate) Medical Director - Dermatology, EMEA. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "(Associate) Medical Director - Dermatology, EMEA" , Thermo Fisher Scientific

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score
Quiz Challenge

Answer 10 quick questions to check your fit for (Associate) Medical Director - Dermatology, EMEA @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.