Paralegal - Clinical Trials

at  WEP Clinical

London, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate30 Apr, 2025Not Specified31 Jan, 20252 year(s) or aboveGood communication skillsNoNo
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Description:

Are you a proactive and results-driven professional with a passion for Legal? Do you aspire to make a meaningful impact in the pharmaceutical industry, particularly in areas related to pricing and proposals? If so, we have an exciting opportunity for you! Join our team at WEP Clinical and help us bring life-changing treatment solutions to patients worldwide. Our business is growing at WEP Clinical, and many career opportunities are endless. We challenge our team to bring thought-provoking ideas to the table. Join us and see how you can take your career to the next level while significantly impacting patients’ lives!

Responsibilities:

ROLE OBJECTIVES:

The Group is growing fast and expanding its Clinical trial services. As the Group grows, the necessity for legal contracts with customers, sponsors, vendors, and suppliers will increase. You will provide clinical trial support to the Group Head of Legal and Assistant Legal Counsel, internal stakeholders, and Group affiliates, which have subsidiaries in the UK, US, Ireland, and Portugal.

WHAT YOU’LL DO:

  • To assist, advise and provide support and collaborate with the internal stakeholders within the group to align on agreements and organisational goals;
  • Draft, review, revise, negotiate, manage, and identify any associated risks in (as necessary) clinical trial-associated agreements, including data protection aspects, under the guidance of the Group Head of Legal and Assistant Legal Counsel.
  • Support improvements and initiatives within the Integrated Legal Team and internal stakeholders in relation to clinical trials;
  • Ensure deadlines are met and take appropriate action to ensure that work is completed to given timescales.
  • Provide support for continuous improvement in order to manage effective management;
  • Maintain updated knowledge of legal developments in clinical research, including local and international regulations.
  • Prepare, update and review legal department presentations and training materials, including internal Standard Operating Procedures in relation to clinical trials.


REQUIREMENT SUMMARY

Min:2.0Max:15.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Law

Proficient

1

London, United Kingdom