Associate, Pharmacovigilance

Proclinical are recruiting for an Associate, Pharmacovigilance for a CRO. This role is on a permanent basis and is located in Japan.

Responsibilities:

• Conduct data entry within the safety database and/or accomplish suitable tracking of incoming safety information.
• Produce queries for missing or unclear information and follow-up with sites for resolution.
• Write safety management plans for designated studies.
• Uphold basic comprehension of budget and scope of work for allocated projects, guaranteeing compliance and increase of any possible changes within scope.
• The ideal candidate will attend when suitable, both internal and client meetings.
• Evaluate incoming SAE data for accomplishment and precision.
• Other duties may be allocated.

Key Skills and Requirements:

• Educated to a degree level in a scientific-linked, nursing or corresponding discipline.
• At least 1 years of experience in pharmacovigilance such as pre-approval clinical trials.
• A mixture of pertinent experience and education.
• Computer literacy in MS Office applications.
• Communication skills both verbally and in writing.
• An organised individual with a high attention to detail.
• Capable of managing various priorities simultaneously while adhering to suitable and tight timelines.
• Works well independently as well as in a matrix team setting.
• Wiling to travel for business needs.
• Fluency in the English language.
• Comprehension of both medical and scientific vocabulary, principles of clinical assessment of adverse drug events, global guidelines and of reporting needs.
• Comprehension of computer technology and management of interpersonal database systems which involves extraction of data.
• Attains a positive attitude with the ability to engage both diplomatically and professionally to a varied audience within an international setting.
• Exhibits the personalities of someone who is committed, dependable, cooperative, adaptable and flexible when performing tasks.
• Able to anticipate requirements and follow through on all allocated tasks.
• Capable of making sound decisions.
• Ability to manage both confidential and sensitive issues with discretion.

If you are having difficulty in applying or if you have any questions, please contact Erik Tarpley at e.tarpley@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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