Clinical Pharmacology Scientist

Hobson Prior are working alongside a brilliant biotech establishment who have an opening on their team for A Clinical Pharmacology Scientist to join on a contract basis located in Basel. Our client is focused on providing life-changing solutions for various serious illnesses.

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 be accountable for being the main scientific contact who is accountable for authoring final study documents.
• Contribute to planning the IND and NDA papers, the reports for formal regulatory conferences such as EOP1, EOP2, as well as resources used for presentations and replies to regulatory management.
• Guide the constant audit of study data such as PK, PD and safety, as well as assess data outputs for scientific and medical rationality and reliability.
• You will support the planning of the clinical pharmacology factor of the project specific investigators pamphlet.
• Accountable for the scientific features of clinical pharmacology study guideline evolvement, sanction form, eCRF and procedure alterations.
• When needed, you will manage the assessment of clinical pharmacology data such as pharmacokinetics, pharmacodynamics, safety, while networking with operational personnel and investigators, data management, biostatistics and any other associates.
• The ideal candidate will attend and offer science assistance for investigator meetings and supervision workshops.
• Participate in critical serious adverse event (SAE) reconciliation and SAE narratives as well as guide the safety audit of clinical pharmacology studies.

Key Skills:

• Work well in a team environment with the ability to train and mentor on an international level both internally and externally, as well as possess social capabilities.
• Communication skills, both written and verbally with the ability to give presentations.
• Exhibit originality, the ability to think critically, take the initiative and establish awareness.

Requirements:

• Educated to an advanced degree level in a pharmaceutical science, clinical pharmacology science or similar discipline.
• At least 2+ years of experience within a pharma industry assisting with clinical pharmacology studies, NCA data evaluation, regulatory archiving and medical authoring.
• Experience with clinical research, ideally in a pharmaceutical organisation with know-how of ICH GCP and the drug development procedure.
• Familiarity with numerous strategies to PK and PD data analysis such as compartmental, curve-sitting, non-compartmental, etc.
• Knowledge of software such as Phoenix, WinNonlin, as well as Microsoft, google suites and possibly Spotfire.
• Acquaintance with operating on and ideally guiding a team matrixed around the scientific and/or clinical study-related responsibilities.
• Fluency in the English language.
• Capable of processing information, assess data, and reach verdicts based on disputing and the validation based on the rick-benefit evaluation and cost-effectiveness.
• Able to represent function on team(s).
• Reply to general guideline queries and process matters.
• Adhere to the company values which are Commitment, Initiative, Open Two-way Communication, Global Teamwork, Trust, Accountability, Interdependence, Consistency, Empowerment, Sense of Urgency, Pride, Drive to Change, Courageous Leadership, Innovation.

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.