PV Consultant Physician - Zero Hour Contract at Quanticate

, , United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

15 Feb, 26

Salary

0.0

Posted On

17 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical Review, Pharmacovigilance, Signal Detection, Safety Reporting, Medical Monitoring, Clinical Practice, Regulatory Documentation, Communication Skills, Organizational Skills, Attention to Detail, ICH GCP, Data Review, Risk Management, Study Design, Aggregate Reporting, Consultancy

Industry

Research Services

Description

Quanticate International is hiring a Pharmacovigilance (PV) Consultant Physician to support clinical and post‑authorisation safety activities for global pharmaceutical and biotech clients. This position provides medical review and specialised input across safety reporting, medical monitoring, and regulatory documentation. You will work within established procedures and quality standards while applying medical judgement across multiple projects. This is a fully remote position but applicants need to be based in the UK and also be happy with zero hour contract. Key Responsibilities Review and assess individual case safety reports, including medical accuracy checks, narrative review, coding verification, assessment and provision of medical causality comments. Support signal detection activities through regular review of aggregate data. Provide medical input into periodic safety reports such as DSURs and PSURs. Review and contribute to project‑specific Safety Plans and other pharmacovigilance (PV) documents. Provide medical consultancy for pre‑ and post‑marketing activities including study design, protocols, investigator brochures, core safety information and risk management plans. Support medical monitoring across clinical studies, including review of study documents, training of project teams and contributions to regulatory and ethics submissions. Attend investigator meetings and Data Monitoring Committee meetings when required. Provide ongoing medical data review covering adverse events, laboratory results and physical examinations. Offer guidance to investigators and study teams, including emergency unblinding for safety concerns when necessary. Provide 24/7 medical contact as required and liaise directly with sponsor teams. Why Join Us You will be part of a knowledgeable global team and contribute to important drug safety work. The role offers varied project exposure, professional growth and the opportunity to apply clinical expertise within an established CRO environment. Quanticate is the world leading data-focused CRO, and we often work with our customers on their complicated clinical trials which require a high level of statistical programming, statistics and data management input. We need talented individuals to help us fulfil our customers’ needs. Our customers range from top global pharmaceutical companies where you can work as an integrated team member on a world leading clinical program, to small biotechs that are taking their first steps in clinical development We strongly advocate career development providing membership to professional societies, encouraging your involvement in their activities and committees. Together we can help you build the career you want – developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter. About You Medical Doctor qualification. Experience in clinical practice and medical monitoring. Strong background in pharmacovigilance, including ICSR triage, medical review and aggregate reporting. Clear communication skills with the ability to explain clinical reasoning. Strong organisational skills, attention to detail and comfort working to tight timelines. Good understanding of ICH GCP and relevant safety regulations. Proficient in Word, Excel and standard PC tools.

Responsibilities

The PV Consultant Physician will review and assess individual case safety reports and support signal detection activities. They will provide medical input into safety reports and contribute to pharmacovigilance documents.