Clinical Project Scientist - Basel - 12 months contract
Location | Basel-Landschaft |
Discipline: | Clinical Development |
Job type: | Contract |
Salary: | £CHF 69.49 – CHF 86.44 |
Contact name: | Harry Henson |
Contact email: | harry.henson@rbwconsulting.com |
Contact phone: | +44 (0)1293 364 092 |
Job ref: | 33329 |
Published: | 6 months ago |
Duration: | 12 months |
Expiry date: | 22 Aug 2024 11:59 |
Startdate: | ASAP |
RBW Consulting are proud to be partnered with one of the worlds leading Biotech's in their search for multiple Clinical Project Scientists to be based out of Basel for a 12 month contract starting ASAP!
The Clinical Project Scientist will be a key member of the Clinical Science team, responsible for designing and delivering clinical plans and trials in multiple diseases and indications in synergy with the trial/program physician.
The Clinical Project Scientist:
Provides scientific input into trial/program level documents such as protocols and related documents, IBs, briefing books for health authority meetings, clinical overviews and summaries, depending on status of development
Contact with clinical experts to, organize and contribute to expert meetings
Participates at meetings with Health Authorities
Develops a sound understanding of the science and medicine related to trials and programs
Performs literature reviews and acquires medical and scientific knowledge specific to the project/program needs, including competitive landscape
Provides scientific input to trial/program-related medical monitoring activities
Represents the trial/program along with the clinical program physician at internal and external meetings
Candidate Requirements:
PhD, Pharm D, MSc or equivalent university degree in life sciences, with passion for clinical science (data review, interpretation, from own or others' clinical research)
Extensive experience (10 years minimum) within a contract research organization (CRO) or pharmaceutical company in all aspects of the planning, setting up, conducting, closing, and reporting of phase II and III clinical studies from a scientific and operational perspective (proven record of delivering clinical study results)
Experience in Rare/Orphan Diseases
Previous experience in authoring clinical study protocols, ICFs, scientific trial related documents (e.g., study committee charters, CSR, CRF, SAP)
Solid experience with data review/medical monitoring of clinical trials
Previous program (project) level experience within a clinical development program
Scientific contribution to documents such as IBs, briefing books for health authority meetings,
Paediatric Investigational Plans (PIPs), clinical overviews and summaries
Participation in life cycle activities for a compound
Solid understanding of Medical Affairs requirements and previous collaboration
Previous exposure to preclinical development activities highly desirable
Demonstrated ability to organize and contribute to scientific discussions with external experts
Expert knowledge of drug development and clinical trial process
Expert knowledge of regulatory requirements/ICH guidelines
Excellent organizational and problem-solving skills with the ability to work under pressure and meet short timelines
Inspires and convinces others, gaining agreement from people, lobbies and networks effectively with key stakeholders
Demonstrated ability to work both independently and in teams in a fast-paced environment, to prioritize multiple competing tasks, to proactively address issues and demands and to discriminate between situations requiring, or not, escalation to upper management
Experience of matrix team management required; people management highly desirable
Solid command of spoken and written English language
Please apply here and Harry Henson will be in contact to discuss your application further.
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