Clinical Trial Physician phase I (client-dedicated), EMEA
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Job Location:
Monthly Salary:
Posted on:
9 hours ago
Vacancies:
1 Vacancy
Job Summary
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
At Thermo Fisher Scientific youll 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.
As a Clinical Trial Physician you will provide clear medical leadership in the Study team working in close collaboration with the other members of this cross functional team in order to provide reliable high quality study data within time and budget .
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 countries in the last 5 years.
What Youll Do:
- Provide medical leadership to the study teams including creating clinical trial protocols while implementing the latest scientific information contribute to site selection contribute to 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 escalation and correction of issues in consultation with the Global Medical Indication Lead
- Interpret the clinical trial data for regulatory documents (e.g. CSR INDs Annual Reports NDAs MAAs etc.) manuscripts and other publications as required in consultation with the Indication Lead
- 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
- In case more than 1 physician is working on the protocol a primus inter pares will be appointed and he/she will ensure that answers to questions from sites /IRBs RAs eligibility and protocol deviation decisions will be harmonized across medics .
Education and Experience Requirements:
- Medical Doctor; relevant specialty education preferred ( e.g. neurology hematology dermatology immunology rheumatology internal medicine pediatric )
- Some experience in industry preferred
.
Knowledge Skills Abilities:
- Excellent English both written and spoken is a must as well as ability to travel.
- Proven interpersonal skills enabling to lead a study team while recognising individual expert competencies providing medical advice and evaluations exercising judgement in which issues need to be escalated immediately
- Pro-active problem solver with negotiation skills remaining sensitive to the different cultural needs in a global organisation
- Strong communication skills to ensure close collaboration with the cross functional team members so that study plans and status are transparent and that risks issues and results are clear to all involved parties. A matrix structure requires additional skills in gathering decision information negotiation and communicating decisions and action.
Working Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.
Why join us
When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experienceand where your contributions truly make a difference.
Apply today to help us deliver tomorrows breakthroughs.
Required Experience:
IC
Key Skills
- EMR Systems
- Post Residency Experience
- Occupational Health Experience
- Pain Management
- SOAP
- Primary Care Experience
- Medical Management
- Suturing
- Workers' Compensation Law
- Pharmacy Residency
- Botox Experience
- Epic
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
