Job Description

Hobson Prior are currently seeking for a Clinical Scientist Director to join a brilliant pharmaceutical organisation on a permanent basis located in Watertown. Our client is focused on

Please note that to be considered for this role you must have the right to work in this location.

Key Responsibilities:

• For this position, you will guide the clinical study protocol/amendment development process by translating the method and approved idea into implementable, effective clinical protocols and connected documents.
• The ideal candidate will develop good, tactical solutions to concerns and work alongside the clinical study team to guarantee problem resolutions.
• Work with others on evaluating, analysing and comprehending the study outcomes and guarantee suitable data evaluation and precise date reporting.
• Recognise study concerns and program concerns by evaluating and supervising developing clinical data connected to safety, efficiency and PK/PD.
• Partake in the clinical method, which involves selection of indications and mixtures.
• You will perform literature evaluations when required for study rational, and the comprehension of study data and development of next steps.
• Collaborate with the medical supervisor to guarantee they are notified of relevant study information, which may involve safety and efficient data.
• Uphold present expertise on the external setting to assure scientific innovations are considered and/or incorporated into clinical trial development method.
• You will serve as a clinical science representative on cross-functional teams as allocated.
• Any other assigned duties.

Key Skills:

• Works well with others.
• An organised individual with the ability to work on various tasks simultaneously.
• Interpersonal capabilities.
• Expertise on GCP, ICH regulations and present EU EMEA and US FDA guidelines.
• A self-starter who is resourceful and energetic.
• You will approach challenges with creativity and pragmatism.
• Communication skills both verbally and in writing.

Requirements:

• Educated to an advanced degree level in a clinical or scientific field.
• At least 10+ years pf experience in planning, implementing, reporting and publishing clinical studies in a pharmaceutical and/or clinical site.
• Capable of evaluating and summarising study data, which involves familiarity in preparing and presenting data.
• Fluency in the English language.
• Comprehension of the drug development process from pre-clinical steps via registration and post-registration.
• Comprehension of trial design and statistics to implement knowledge to the design of clinical protocols.
• Able to comprehend, analyse and present clinical data which involves aggregate data analysis to notify decision-making and set clinical method.
• Prior involvement in conducting systematic literature search, summarising the search results and presenting the conclusions to a broad spectrum of audiences.
• Capable of engaging the team to accomplish objectives without direct authority.
• A driven individual to move the clinical programs forward while maintain quality.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

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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