Nos aseguraremos de que las personas con discapacidades reciban adaptaciones razonables para participar en el proceso de solicitud de empleo o entrevista de trabajo, para que puedan ejercer las funciones de trabajo esenciales y recibir otros beneficios y privilegios del empleo. Comuníquese con nosotros para solicitar una adaptación.
(Associate) Medical Director - Neurology, Western Europe (Client-Dedicated)
Share job link
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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 Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the PPD and client`s environment.
We are looking for neurologists with expertise in Peadiatrics Neurology or Neuromuscular diseases.
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. Provides protocol and study compound overview at the 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
Qualifications - External
Education
- MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Neurology patients in hospital practice
Knowledge, Skills, Abilities
- 3 – 5 years of experience within pharmaceutical industry, clinical trials and pharmaceutical medicine is critically important
- 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.
Recibe notificaciones de trabajos similares
¡Error!
Recomendaciones de perfil
Trabajos similares
-
(Associate) Medical Director - Neurology
Id. del empleo R-01281651
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 ap...
-
(Senior) Medical Director - Rheumatology (Client - dedicated), EMEA
Id. del empleo R-01291460
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 ap...
-
Clinical trial coordinator - FSP
Id. del empleo R-01306115
CTC works cross-functionally, with internal and external partners, on clinical study management activities, as agreed with the Study Delivery Lead, for in-house and outsourced studies across all phase...
-
Clinical Site Liaison (Neurology/ Rare Disease) - FSP
Id. del empleo R-01292707
Proactively work to fully understand all matters that impact the successful patient recruitment and high quality conduct of the clinical trial at each site, eg the Principal Investigator (PI) and site...
-
Sr Clinical Trial Coordinator - Client-dedicated - Belgium
Ubicación Brussels, Bélgica Id. del empleo R-01292614
Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific train...
-
Senior/Clinical Research Associate II - Client Dedicated
Ubicación Remote, Bélgica Id. del empleo R-01306529
Discover Impactful Work. Have excellent communication and interpersonal skills and are looking to work in a collegiate environment where you want to take true ownership for your work. Independent, on-...
-
Senior Clinical Team Manager - Non Interventional Studies
Id. del empleo R-01304139
Ensures achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the...
-
Medical Science Liaison (Renal Transplant), FSP
Id. del empleo R-01299622
The Medical Science Liaison (MSL) is a field-based expert on scientific data, products and trials, responsible for engagement with medical stakeholders at Clinical Trial Centers (Kidney Transplant Stu...
-
CRA/Senior CRA - Belgium
Ubicación Remote, Bélgica Id. del empleo R-01307064
Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights,...
Los solicitantes de empleo también vieron
Nos aseguraremos de que las personas con discapacidades reciban adaptaciones razonables para participar en el proceso de solicitud de empleo o entrevista de trabajo, para que puedan ejercer las funciones de trabajo esenciales y recibir otros beneficios y privilegios del empleo. Comuníquese con nosotros para solicitar una adaptación.