Senior Clinical Scientist (m/w/d)

Lausanne |

Freelance

Job title: Senior Clinical Scientist Consultant (m/w/d)

Industry: Pharma
Skills: Clinical Affairs

Start of project: 01.06.2023 (Potential)

Duration of the project : 6 Months +

Project volume: TBD

Location: Lausanne

Tasks:

Drive development of protocols/protocol amendments for clinical studies
Prepare and/or provide input to clinical study related and other regulatory documents (e.g. CSRs, IBs, PIS/ICFs, SAPs, Data Management Plans, Safety Management Plan, Medical Monitoring Plan, SRC Charter, IND, briefing books)
Prepare and/or provide input to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., IB, DSUR, regulatory responses)

Qualifications:

Master's in Life Sciences, Pharmacist or PhD in Life Sciences (preferred)
At least 7-10 years of relevant experience in clinical development within the pharmaceutical industry, including development of CDPs and protocols
Experience in conducting Clinical Studies in Oncology

Referenznummer:

Branche:

Beginn des Projekts:

Dauer:

Anstellungsart:

Kontakt

Bella Iglesias

12977

Pharma

Ab sofort

n. A.

Freelance