This job is with Thermo Fisher Scientific, an inclusive employer and a member of myGwork – the largest general platform for the LGBTQ+ business community. Please do not contact the recruiter directly.Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt 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.¿Es usted el candidato adecuado para esta oportunidad? Asegúrese de leer la descripción completa a continuación.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 2,700 clinical trials across 100+ countries in the last 5 years.What You'll 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 trialsReal 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 LeadInterpret 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 LeadMedical 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 indicationsEnsure study compliance for all medical aspects

by understanding and applying all relevant SOPs and GCPClosely collaborate

with the cross functional study

team members in order for

medical

risks, issues, and results to be

clear to all involved partiesIn 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 organisationStrong 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. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference. xqbhyrx Apply today to help us deliver tomorrow’s breakthroughs.

📌 Clinical Trial Physician - phase I (client-dedicated), EMEA (Madrid)
🏢 Thermo Fisher Scientific
📍 Madrid