(Senior) Clinical Project Coordinator at BD Becton Dickinson UK
Berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

18 Dec, 26

Salary

50000.0

Posted On

19 Sep, 26

Experience

13 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Pharmaceutical Manufacturing

Description

Required Skills & Competencies

  • Bachelor’s Degree (BS/BA) in life sciences or equivalent combination of training and experience (MA/MS preferred)
  • 1+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology), with supply inventory management/shipment, or in a clinical setting
  • Proficiencywith Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)
  • Strong interpersonal and communication/presentation (oral and written) skills
  • Strong organizational skills, attention to detail, criticalthinkingand analytical skills
  • Able to manage and delegate multiple tasks and prioritize importance of tasks/projects

Preferred Qualifications:

  • Knowledge of domestic and international clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies
  • Knowledge of clinical study processes and systems (eTMF, CTMS andCEDMS). Prior experience with Veeva Vault preferred.
  • 1+ years of experience with similar role for a Sponsor or Contract Research Organization (CRO)


Responsibilities

Required Skills & Competencies

  • Bachelor’s Degree (BS/BA) in life sciences or equivalent combination of training and experience (MA/MS preferred)
  • 1+ years of experience in clinical research (medical device, pharmaceutical and/or biotechnology), with supply inventory management/shipment, or in a clinical setting
  • Proficiencywith Microsoft Suite tools (Outlook, Word, Excel, PowerPoint, OneNote, To-Do, SharePoint, etc.)
  • Strong interpersonal and communication/presentation (oral and written) skills
  • Strong organizational skills, attention to detail, criticalthinkingand analytical skills
  • Able to manage and delegate multiple tasks and prioritize importance of tasks/projects

Preferred Qualifications:

  • Knowledge of domestic and international clinical research regulations and guidelines, Good Clinical Practice (GCP) and current industry practices related to the conduct of clinical studies
  • Knowledge of clinical study processes and systems (eTMF, CTMS andCEDMS). Prior experience with Veeva Vault preferred.
  • 1+ years of experience with similar role for a Sponsor or Contract Research Organization (CRO)

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