Skip to main content
Αναρτήστε το βιογραφικό σας - Χρειάζονται μόνο μερικά δευτερόλεπτα

gcp medical εργασίες

Ταξινόμηση ανά: -
25+ θέσεις εργασίας
    • The Medical Director will provide medical support and medical advice for clinical trials and safety evaluation within the PPD Pharmacovigilance department.
    • Προβολή όλων των θέσεων εργασίας θέσεις εργασίας: Thermo Fisher Scientific - Απομακρυσμένη Εργασία - θέσεις εργασίας: Medical Director - Απομακρυσμένη Εργασία
    • Αναζήτηση με μισθό: Associate Medical/Medical Director - Nephrology, EMEA μισθοί
    • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol,…
    • Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol,…
    • Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including verifying the…
    • ️ Private medical health insurance plan.
    • You will work on integrating Large Language Models (LLMs) into real-world solutions.
    • As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and…
    • By effectively managing resources, coordinating teams, and ensuring adherence to protocols, these roles contribute to the advancement of medical knowledge and…
    • Our platform delivers high-performance user experience, zero trust security and operational cost efficiency regardless whether customers require cloud, on-…
    • Excellent command (written and verbal) of English language and proficient knowledge of medical terminology.
    • The Clinical Operation Manager is responsible for…
    • Their contributions are essential for advancing medical knowledge and improving patient outcomes.
    • Conduct on-site and remote monitoring of clinical research…
    • Conducts source document review and verification or appropriate site source documents and medical records.
    • Ensures regulatory, ICH-GCP, and protocol compliance.
    • Their contributions are essential for advancing medical knowledge and improving patient outcomes.
    • Conduct on-site and remote monitoring of clinical research…
    • You’ll work directly with cross-functional teams to ensure Sword’s products are robust, scalable, and secure, empowering both our internal and external users…
    • Contribute to designing, building, evaluating, shipping, and improving Sword’s products by hands-on AI/ML development;
    • Manage and execute the site identification process in accordance with regulations, SOPs, and project requirements, ensuring timely and accurate completion of…

Job Post Details

Associate Medical/Medical Director - Nephrology, EMEA - job post

Thermo Fisher Scientific
3.4 από 5 αστέρια
Απομακρυσμένη Εργασία
Δημιουργήστε έναν λογαριασμό Indeed προτού συνεχίσετε στον ιστότοπο της εταιρείας.

Στοιχεία θέσης εργασίας

Τύπος θέσης εργασίας

  • Πλήρης απασχόληση

Τοποθεσία

Απομακρυσμένη Εργασία

Πλήρης περιγραφή θέσης

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 Medical Director will provide medical support and medical advice for 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

  • MD, MB/BS or equivalent degree and strong medical knowledge, shown clinical experience running Nephrology patients in hospital practice

Knowledge, Skills, Abilities

  • Significant 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.

Κάντε εύκολα αίτηση για θέσεις εργασίαςΑναρτήστε το βιογραφικό σας