Hobson Prior are currently seeking a Global Benefit Risk Management, Scientist Manager to join a fantastic biotech establishment on a contract basis located in Uxbridge with flexible working available. Our client is focused on uncovering, developing, engineering, and distributing ground-breaking therapeutics for patients suffering from 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 responsible for representing the actions of benefit-risk management procedure preparation within internal and external groups.
• Look to integrate the patient outlook into benefit-risk progressions and deliverables.
• Portray risks associated with the company project, recognise the best approaches for minimal risk and extent of efficiency for said minimal risk procedures.
• To guarantee that product benefit-risk management approaches are evolved internationally on a continuous basis, you will be offering your expertise in consultations and support the allocated therapeutic areas.
• The ideal candidate will progress and sustain corresponding standards and schedules.
• To target developing pharmacovigilance abilities in correlation to benefit-risk organisation, you will partake in cross-functional proposals.
• Assist with inspecting and auditing actions concerning the BRM procedures within Safety.
• To warrant steadiness across the company's products approximating benefit-risk management internationally, you will offer insight.
• The ideal candidate will guarantee that the company follows and is affiliated with Global Health Authority protocols vis-à-vis benefit-risk management customs.
• To verify that the company complies with global benefit-risk management standards, you will be accountable for overseeing the benefit-risk management metrics and documents.
• Any other assigned duties.

Key Skills:

• Exceptional communication abilities, both written and verbally with presentation capabilities.
• Operates well independently with the ability to implement networking and inspiring proficiencies.
• Works well in-person and remotely with a team consisting of product teams/leaders/managers.
• Able to multitask multifaceted projects concurrently.

Requirements:

• Educated to a degree level: either a Doctorate; a master's with 3 years of pharmacovigilance experience; a bachelor's with 5 years of pharmacovigilance experience; an associate's degree with 10 years of pharmacovigilance experience; or a high school diploma / GED with 12 years of pharmacovigilance experience.
• Would be ideal to be educated to a B.S., M.S. degree level in health services research, behavioural medicine, public health, or a similar discipline.
• Ideally at least 3 years of experience in a pharmaceutical or device industry with at least 1 year of global drug safety and risk management experience.
• Experience guiding and handling teams.
• Knowledgeable of international features of drug safety.
• Understanding of industry ideologies of drug development and pharmacology, biostatistics, clinical trial methodology, and pharmacoepidemiology.
• Solid comprehension of global safety documenting actions, guidelines and procedures.
• Familiarity with risk management protocols and drug development procedures.

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.