Lead Clinical Development Scientist
Il y a 2 mois
Hobson Prior are currently seeking for a Lead Clinical Development Scientist to join a brilliant pharmaceutical organisation on a contract basis located in Gosselies. Our client is focused on developing ground-breaking remedies.
Please note that to be considered for this role you must have the right to work in this location.
**Key Responsibilities**:
- For this role, you will guide the clinical study protocol/change development procedure by translating the method and agreed ideas into implementable, effective clinical protocols and connected documents.
- Partake in the clinical method, which involves selection of indications and combinations.
- Collaborate with the medical supervisor to guarantee he/she is notified of pertinent study information, which may involve safety and efficient data.
- You will work together on the evaluation, examination and comprehension of study outcomes and ensure suitable data evaluation and precise data reporting.
- Recognise study and program problems by evaluating developing clinical data linked to safety, efficiency and PK/PD.
- Perform literature reviews when required for study rational, and the comprehension of study data and development of next steps.
- Any other assigned duties.
**Key Skills**:
- Works well in a team.
- An organised individual with documentation and interpersonal abilities.
- Able to make decisions and set clinical methods.
- Communication skills both verbally and in writing.
**Requirements**:
- Educated to an advanced degree level in a clinical or scientific discipline.
- At least 5+ years of experience within a clinical, technical/operational role, planning, implementing, reporting and publishing clinical studies in the pharmaceutical organisation and/or at clinical sites.
- Capable of evaluating and summarising study data, which involves preparing and presenting data.
- Fluency in the English language.
- Comprehension of the drug development procedure from pre-clinical steps through registration and post-registration.
- Comprehension of the functional areas of drug development and clinical operations.
- Understanding and ability to discuss clinical information.
- Comprehension of trial design and statistics to implement expertise to the design of clinical protocols.
- Familiarity conducting systematic literature search, summarising the search outcomes and displaying the conclusions to a varied audience.
- Expertise on GCP, ICH regulations and present 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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