Clinical Scientist (hybrid)

Job content

Proclinical are working alongside a global biotech organisation who have an opening in their company. The client is currently recruiting for a Clinical Scientist. This role is located in Basel, is on a contract basis and allows hybrid working. This client is focused on distributing life-changing therapies all around the world.

Responsibilities

• You will handle the development and writing of study documentation involving protocols, apprised consent forms, clinical study reports, as well as clinical science input for study-specific operational and regulatory documents.
• Offer coaching and science input to operation colleagues and study site staff.
• Stay at the forefront of scientific and technical excellence by collaborating with the scientific community, contributing to presenting and issuing high-quality scientific abstracts, posters, articles and partaking in key conferences.
• Contribute to experimental medicine studies and/or projects in collaboration with internal or external Partners.
• The ideal candidate will oversee study progress on a regular basis to recognise any complications or issues that could have an impact on the results or completion of the study.
• Accountable for ongoing monitoring of clinical activities and study conduct, coordination of data collection, data cleaning and review, analysis, and clarification as well as formulation and exhibition of results for informed decision-making.
• Partake in study management as clinical science representative to guarantee trial deliverables are met according to timelines, budget, quality standards and operational procedures, within a global multidisciplinary cross-functional Study Management Team (SMT).
  

Skills & Requirements

• At least attained a PhD in an applicable scientific topic (e.g. Neuroscience, Pharmacology, Psychology // PhD, Pharma D or MD).
• At least 2-3 years of experience in Clinical Science (involving: conducting on ongoing trials, alliance with the operations team, vendor, site management).
• Pharma / Medical Industry experience is mandatory for this role.
• Previous experience in drug development and clinical trials methodology and execution (Phase 0-2).
• Proven track-record of impactful scientific exploration.
• Ability to obtain knowledge in different disease suggestions and therapeutic areas.
• Capable of collaborating and thriving in a matrix setting and co-operate with a variety of individuals outside (e.g. investigators, partners, KOLs) and inside the company (e.g. regulatory affairs, biostatistics, clinical pharmacology, project management).
• Highly experienced with clinical data review, analysis, interpretation and reporting.
• Exceptional analytical and quantitative skills.
• Acquainted with ICH-GCP regulation and regulatory guidance documents about clinical trials.
• Solid project-management skills and aptitude to prioritise tasks in a dynamic atmosphere.
• Brilliant written and oral communication skills in English.
• Sturdy communication skills and facility to interact in a cross-functional matrix and represent science in study management teams, projects team and across the whole organisation.
• Competence and willingness to distribute scientific output in relation to clinical trial results.
• Former experience in Neuroscience as a Clinical Scientist (especially in movement disorders and/or neurodegeneration) is desirable, but not essential to the role.
  

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Mohammed Alli on +41 61 568 79 85.

A Full Job Description Is Available On Request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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