Director - Lead Clinical Development Scientist
il y a 3 semaines
Hobson Prior are seeking for a Director - Lead Clinical Development Scientist to join a brilliant pharmaceutical establishment on a permanent basis located in Gosselies. Our client is focused on developing ground-breaking remedies that are aimed at treating cancer and improving the immune system.
Please note that to be considered for this role you must have the right to work in this location.
**Key Responsibilities**:
- Guide the clinical study protocol/amendment development procedure by translating the method and sanctioned notion into implementable, effective clinical protocols and linked documents.
- Collaborate with the medical supervisor to guarantee they are notified of relevant study information, which involves safety and effectiveness data.
- Work alongside others on the evaluation, analysis, and comprehension of study outcomes and ensure suitable data evaluation and precise data reporting.
- You will recognise study and program concerns by evaluating and supervising developing clinical data linked to safety, efficiency and PK/PD.
- Conduct literature reviews as needed for study rational, and the interpretation of study data and development of next steps.
- Any other assigned duties.
**Key Skills**:
- Communication skills both verbally and in writing.
- Works well in a team setting.
- An organised individual with the ability to document and work on various tasks simultaneously.
- Interpersonal abilities.
**Requirements**:
- Educated to an advanced degree level in a clinical or science discipline.
- At least 5+ years of experience in planning, implementing, documenting and publishing clinical studies within a pharmaceutical organisation and/or clinical sites.
- Capable of evaluating and summarising study data, which involves familiarity with planning and displaying data.
- Fluency in the English language.
- Comprehension of the drug development procedure form pre-clinical steps through registration and post-registration.
- Comprehension of trial design and statistics to implement expertise to the design of clinical protocols.
- Able to comprehend, analyse and display clinical data, which involves aggregate data analysis to notify decision-making and set clinical tactics.
- Acquaintance with conducing systematic literature search, summarising the search outcomes and displaying the conclusions to a varied audience.
- Expertise on GCP, ICH Regulations and existing EU EMEA and US FDA guidelines.
Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.
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