Scientific Information Manager (m/f)

Basel region  ‐ Onsite
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Keywords

Description


We are looking for a
Scientific Information Manager (m/f)

Reference: -en
Start: asap
Duration: 12 MM++
Place: in Basel region
Branch: Herstellung von pharmazeutischen Erzeugnissen

Your tasks:
  • Contribution to drug development through close monitoring and understanding of disease area treatment trends
  • Ensure that Clinical Development organization is provided with the latest relevant available medical and scientific information on products and/or competitors
  • For compounds in development, identify the key players in the competitive environment and monitor publicly available scientific and medical information on competitor compounds
  • Develop, release and maintain scientific and medical analyses of data collected
  • Ensure the clinical development organization is timely provided with clinical study results in an user- friendly format for interaction with internal and external stakeholders
  • Follow, monitor and understand the laws, regulations and guidelines concerning the mandatory disclosure of clinical trial designs and results in public registries
  • Ensure appropriate and timely communication towards management and other functions involved in the clinical trial conduct about up-coming changes/issues related to the transparency of clinical trial information
  • Manage the preparation of the protocol information and of the study results to be entered in the company registry and ClinicalTrials.gov in a very specific format required by law and regulation
  • Manage the review and approval of all data to be publicly disclosed and ensure release of the information within the required timelines
  • Ensure company efficiency for clinical trial disclosure activities to avoid missed deadlines or incomplete submissions


Your qualifications
  • High academic degree (MD, PhD or PharmD) in medical or life science
  • Solid experiences in a globally operating pharmaceutical or biotech industry with previous exposure to the clinical development environment: clinical trial management, medical writing, regulatory affairs, medical communication or medical information
  • Sound ability to understand, interpret, critically analyze, and summarize complex scientific and medical data
  • Excellent team player
  • Excellent written and oral communication
  • Excellent organizational and interpersonal skills
  • Fluent in English



Skills:
- Medical affairs manager


Keywords: Medical Affairs Manager medical life sciences scientific information manager data
Start date
ASAP
Duration
12 MM++
(extension possible)
From
Hays AG
Published at
09.01.2014
Contact person:
Kerstin Sieber
Project ID:
648553
Contract type
Freelance
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