Stellenangebote für Trial Jobs in Boudry

19 Treffer

Trial Document Specialist

Top Job - Basel (Basel-Stadt)

Throughout study conduct - Support CS in the maintenance of trial documentation - Work with documentation group and/or CRAs/CROs to resolve issues identified during electronic document uploads into internal systems - Review eTMF...

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Medical Affairs - Study Scientist

Top Job - Boudry

The Clinical Development Plan and as approved by the Hematology and Oncology Development Committee for Interventional Clinical Trials or by the Medical Affairs Independent Review Committee for Non-Interventional Post...

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Clinical Trial Coordinator

Top Job - Basel (Basel-Stadt)

You plan, compile, dispatch and coordinate with internal departments and the affiliates, track submissions and approvals in appropriate systems of core clinical trial applications (CTA) or common documents and...

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Medical Affairs - Study Scientist

- Boudry

The Clinical Development Plan and as approved by the Hematology and Oncology Development Committee for Interventional Clinical Trials or by the Medical Affairs Independent Review Committee for Non-Interventional Post...

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Director, Regional Regulatory Disease Lead/ Regional Product Lead

- Boudry

Requirements, development and ownership of the Regulatory Development Plan (RDP), responsibility for Worldwide submission plans and accountability for global regulatory documents such as clinical trial/marketing applications and...

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Director, Regional Regulatory Disease Lead/ Regional Product Lead

- Boudry

Requirements, development and ownership of the Regulatory Development Plan (RDP), responsibility for Worldwide submission plans and accountability for global regulatory documents such as clinical trial/marketing applications and...

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Senior Specialist, Regulatory Projects Team

- Boudry

Requirements. • Contributes to the content of regulatory documents working with other functions as necessary and contributes to the review of documents before submission. • May support the regulatory aspects of clinical trials and...

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Contract Coordinator (in a medical study team) 2 years fixed term contr

- Boudry

Preparation of Investigator Initiated Trial (IIT) contracts on the basis of contract templates, management of the IIT contracting process, maintaining the related information systems up to date, optimization of the IIT...

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Medical Director, Clinical Research Physician

- Boudry

Minimum > in Hematology/Oncology Direct industry experience is preferred; substantial experience working on industry-sponsored trials will...

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Director, Regional Regulatory Disease Lead/ Regional Product Lead

- Boudry

Regulatory Development Plan (RDP), responsibility for Worldwide submission plans and accountability for global regulatory documents such as clinical trial/marketing applications and for interactions with global Health Authorities...

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Medical Director, Clinical Research Physician

- Boudry

Description Pre-requesites Minimum degree and substantial medical/clinical training in Hematology/Oncology Minimum > in Hematology/Oncology...

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Medical Director, Clinical Research Physician

- Boudry

Description Pre-requesites Minimum degree and substantial medical/clinical training in Hematology/Oncology Minimum > in Hematology/Oncology...

Merkenstellenanzeige.monster.de

IT Contract Coordinator

- Boudry

Business, advance our science and contribute to our unique culture. Summary/Scope Preparation of Investigator Initiated Trial (IIT) contracts on the basis of contract templates, management of the IIT contracting process...

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Medical Affairs - Study Scientist

- Boudry

The Clinical Development Plan and as approved by the Hematology and Oncology Development Committee for Interventional Clinical Trials or by the Medical Affairs Independent Review Committee for Non-Interventional Post...

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Clinical Trial Coordinator

Top Job - Basel (Basel-Stadt)

Clinical Trial Coordinator Objectives and Scope of PositionResponsible to provide support to Regulatory Program Managers on overall operational management of Clinical Trials Application in EU/International countries You...

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Sr. Pharmacovigilance Leader

Top Job - Basel (Basel-Stadt)

Signals based on a comprehensive evaluation of post-marketing data and Serious Adverse Events (SAEs) from clinical trials. Major Accountabilities 1. Monitors the clinical safety of projects/products and responds appropr...

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