Barrington James
Safety Physician

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FREELANCE SAFETY PHYSICIAN
I am partnered with a leading Biopharmaceutical company who have a strong commitment to innovation and a wide variety of therapeutic areas who are looking to add an experienced and medically driven Safety Physician to their expanding team.
Remote Work structure Competitive pay rate 12 Month contract Full time
In this role as a Safety Physician, you will provide medical and clinical oversight across the drug lifecycle, from early clinical development through to post marketing, leading medical review of adverse events, causality assessment and benefit-risk evaluation. This role is vital to people who want to bring strong clinical judgement to patient safety and people with an eager attitude to protecting patients throughout a product's life.
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I’m in my final year doing Economics and I don’t know whether to apply for grad schemes now or do a masters first. What do you think?
Honest answer — it depends on where you want to end up. A lot of top grad schemes (Big 4, civil service, banking) don’t need a masters. Let’s look at the ones you’d be competitive for now, and we can decide if a masters actually adds anything.
Also worth knowing: most autumn 2026 applications are open now. Timing matters more than you think.
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Graduate Consultant — 2026 Scheme
Why you're a good match
StrongYour economics background and your summer at a regional bank line up with what PwC looks for on the consulting scheme. Applications close in four weeks.
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Why you're a good match
You’ve got the grades and the economics background, and your bank internship is exactly the experience this scheme looks for. Apply soon — deadlines close within the month.
Experience fit
Your summer at the bank plus your econometrics coursework map directly to the day-one responsibilities on this scheme — client modelling, market briefings, and deal support.
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No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Key Responsibilities
- Provide medical oversight of drug safety activities across the product lifecycle.
- Lead medical review, causality assessment and signal evaluation for individual and aggregate safety data.
- Support preparation and review of safety reports and regulatory documents.
- Contribute medical expertise to benefit-risk decisions and risk management plans.
- Work with global cross-functional teams to maintain patient safety standards.


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Experience You Should Bring
- Strong clinical and pharmacovigilance experience within the pharmaceutical industry.
- Knowledge of GxP, regulatory requirements, and clinical trial processes.
- Experience with medical review, safety signal evaluation, and benefit-risk assessments.
- Ability to interpret complex clinical and safety data and communicate findings clearly.
- A medical degree (MD or equivalent) required, with experience working in global teams.
If this role sounds like it's for you…Apply now
For further information/questions please message me via LinkedIn
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