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298 offres d'emploi Clinical Trial Manager -


Clinical Supply Chain Manager

Lieu : Rixensart Wallonia
Société : 1054 GlaxoSmithKline Services Unlimited

ICH and GCPs.Experience working with senior leadership including but not limited to Clinical Operations,..This role supports Phase I through IV GSK sponsored clinical studies as well as investigator sponsored trials and compassionate use programs.Leads the cross-functi..

Postuler | Plus d'offres Clinical Supply Chain Manager
Plus d'offres - Rixensart


Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

Biopharmaceutical experience would provide a strong advantage3) Additional 4+ years direct experience in clinical trial management4) Solid track record in successfully executing Phase I – III clinical trials5) Demonstrated expert knowledge and comprehensive un..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

and medical safety reporting7) Knowledge of electronic data capture systems and web-based clinical trial management tools8) Excellent interpersonal,..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

hands-on manager with experience in managing Core Labs,..BSN or RN or higher degree in the Life Sciences or related disciplines2) Minimum 3+ years in clinical management position in biopharmaceutical or device industry,..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

Biopharmaceutical experience would provide a strong advantage3) Additional 4+ years direct experience in clinical trial management4) Solid track record in successfully executing Phase I – III clinical trials5) Demonstrated expert knowledge and comprehensive un..

Postuler


Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

and key opinion leaders to optimize the clinical development programsParticipate in the development of SOPs and work instructions to assure internal files and clinical study files (patient;..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

sites and vendors required for conduct of clinical trialsDirect/Manage necessary clinical trial approvals from IRBs/ECs,..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

Additional responsibilities include management of clinical trials approvals with local IRBs and/or Competent Authorities.Required Skills and Experience:1) BS,..

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Clinical Affairs Program Manager Belgium

Lieu :
Société : Chronos Consulting

Biopharmaceutical experience would provide a strong advantage3) Additional 4+ years direct experience in clinical trial management4) Solid track record in successfully executing Phase I – III clinical trials5) Demonstrated expert knowledge and comprehensive un..

Postuler


Clinical Project Manager - Sponsor Dedicated - Anywhere in EMEA

Lieu : Brussels Brussels
Société : IQVIA

troubleshoot and influence for quality and deliveryA track record of ensuring GCP compliance and successful risk management of complex clinical studies is expectedAbility to travel as required internationally and domestically...

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Clinical Project Manager - Sponsor Dedicated - Anywhere in EMEA

Lieu : Brussels Brussels
Société : IQVIA

troubleshoot and influence for quality and deliveryA track record of ensuring GCP compliance and successful risk management of complex clinical studies is expectedAbility to travel as required internationally and domestically...

Postuler


Clinical Project Manager - Sponsor Dedicated - Anywhere in EMEA

Lieu : Brussels Brussels
Société : IQVIA

PharmD) is preferred.8+ years of clinical research experience in biopharma or CRO4+ years of clinical project management wit regional or global scopeDemonstrated project management skills across multiple highly complex clinical studiesExperience of managing multiple st..

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Clinical Project Manager - Sponsor Dedicated - Anywhere in EMEA

Lieu : Brussels Brussels
Société : IQVIA

A clinical or advanced degree (RN,..technology solutions and clinical research services to the life sciences industry...

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Clinical Operations Development Lead

Lieu : Ghent Flanders
Société : Argenx

ensures the CDP describes the clinical development strategy,..clear way and energizes and motivates the CDT team members as well as the respective CTMs to work towards achieving the clinical goals in line with the OGSM and argenx’ cultural pillars.If applicable,..

Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent


Clinical Operations Development Lead

Lieu : Ghent Flanders
Société : Argenx

A CDT kicks off as soon as preparations start for a First in Human (FIH) study (in the case of the first indication for a given compound) or when first clinical related discussions start for a new indication.To build a strong CDT,..

Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent


Clinical Operations Development Lead

Lieu : Ghent Flanders
Société : Argenx

ensures the CDP describes the clinical development strategy,..by ensuring that lessons learned are shared across trials within the assigned therapeutic indication,..

Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent


Clinical Operations Development Lead

Lieu : Ghent Flanders
Société : Argenx

local and global/international trial management).Experience in working in an outsourced model,..PhD degree is a plus.Minimum of 10 years of leading experience in Clinical Development (monitoring,..

Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent


Clinical Operations Development Lead

Lieu : Ghent Flanders
Société : Argenx

the CODL may also act as a CTM for 1 or more selected trials.The CODL function may include line management of Clinical Trial Manager(s) (CTMs) and/or Clinical Trial Associate(s) (CTAs).Roles & Responsibilities:Provides strategic input and is accoun..

Postuler | Plus d'offres Clinical Operations Development Lead
Plus d'offres - Ghent


Clinical Supply Partnering Associate

Lieu :
Société : Keyrus Life Science

ensuring that clinical trial specifics needs are met...this approach has allowed us to become a key player in clinical research...

Postuler | Plus d'offres Clinical Supply Partnering Associate


Clinical Operations Program Director - Biotech

Lieu : Brussels Brussels
Société : Proclinical

they're seeking several Clinical Operations Program Directors to strengthen our clients Global Clinical Trial Operations team...

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Clinical Operations Program Director - Biotech

Lieu : Brussels Brussels
Société : Proclinical

- Accountable for all clinical-related aspects within the assigned therapeutic indication/program...- Minimum of 10 years of leading experience in Clinical Development/ Operations within a biotech/ pharma - Experience in working in an outsourced model,..

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Clinical Operations Program Director - Biotech

Lieu : Brussels Brussels
Société : Proclinical

- Rare diseases experience would be a plus.About Proclinical:..- Act as primary point of contact for all clinical-related activities for a given indication or across asset indications...

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Clinical Operations Program Director - Biotech

Lieu : Brussels Brussels
Société : Proclinical

Follow us and check out our website for live roles and updates www.proclinical.com","datePosted":"2024-03-28T17:16:48+00:00","validThrough":"2024-05-12T17:16:48+00:00","employmentType":["Permanent"],"hiringOrganization":{"@type":"Organization","name":"Proclinical","image":"ht..

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Regulatory Affairs & Compliance, Associate Manager / Manager

Lieu : Zaventem Flanders
Société : Zoetis

..Associate Manager / Manager.JOB PURPOSE:In collaboration with the RA team members,..CORE RESPONSIBILITIES:Regulatory Affairs:With the other Regulatory team members,..

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Regulatory Affairs & Compliance, Associate Manager / Manager

Lieu : Zaventem Flanders
Société : Zoetis

..Associate Manager / Manager.JOB PURPOSE:In collaboration with the RA team members,..Zoetis is currently looking for a Regulatory Affairs & Compliance,..

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