Regulatory Affairs Associate
1 day ago
Are you seeking an exciting and fulfilling new opportunity? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a mission-driven organisation dedicated to advancing clinical research and transforming lives.
We are posting this role now and will be reviewing applications on a rolling basis between now and Christmas. Interviews will begin in the New Year, so you may experience a brief delay in hearing back from us during the holiday period. Thank you in advance for your patience - we look forward to connecting in January.
Role Objectives:
The WEP Clinical Regulatory Affairs Associate is responsible for supporting regional regulatory function with the regulatory operational direction and support at WEP Clinical.
The Ideal Candidate:- Discrete
- Highly Organised
- Detail Oriented
- Strong Communicator
- Support the team in guiding the business, regarding current regional regulations ex-US in the compliant movement of pharmaceutical products
- Communicate with regulatory agencies as needed to support the development of the regulatory database of country-specific information
- Support the growth of the regulatory database of country-specific information with the creation of country summaries
- Support the team in carrying out country-specific research as needed
- Keep up to date with all applicable regulatory changes towards the procurement, movement, and distribution of unlicensed medicines
- Work in the regulatory affairs department on various assigned projects
- Help provide regulatory support to the project management team.
- Bachelor's Degree (in a health or science field preferred)
- Basic knowledge or exposure to Regulatory affairs, preferred
- Ability to meet multiple tasks and meet deadlines in a fast paced environment
- Effective verbal and written communication skills
- Strong organizational skills and attention to detail
- Computer literacy and proficient in Microsoft Office
- Highly self-motivated with strong interpersonal skills
- Ability to effectively research and summarise findings
- Ability to interpret legislation and assess requirements
- Ability to handle confidential information with complete discretion
What We Offer:
Private healthcare insurance
Long-term illness Cover
Death in service cover
Salary sacrifice pension
Annual leave
Paid maternity & paternity leave
Volunteer day
What sets us apart:
WEP Clinical partners with sponsors to help patients and physicians gain early access to medicines when no other treatment options are available. WEP Clinical has over 15 years of experience distributing products to more than 120 countries worldwide, addressing unmet patient needs.
We're Committed to Our Team:
WEP has many initiatives to encourage wellness, growth, development, and team relationships. Check out our LinkedIn Life Page to learn more about our team events and all that we do to support our employees.
We're Committed to DEI:
At WEP Clinical, acceptance, recognition, and engagement are the core values of our DEI. We are committed to providing employees with opportunities for personal and professional growth and success, embracing everyone's unique identities.
Our services include:
Access Programs
Clinical Trial Services
Patient Site Solutions
Clinical Trial Supply
Market Access and Commercialisation
WEP Clinical is a smoke-free, drug-free, and alcohol-free work environment.
WEP Clinical is an equal-opportunity employer. WEP Clinical does not unlawfully discriminate against employees or applicants for employment based on an individual's race, colour, religion, creed, sex, sexual orientation, gender identity or expression, national origin, genetic information, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions, and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. WEP Clinical will make reasonable accommodation for qualified individuals with known disabilities, in accordance with applicable law.
-
Associate Director, Regulatory Affairs
5 days ago
London, Greater London, United Kingdom Shionogi Europe Full time £80,000 - £120,000 per yearDescriptionShape the Future of Regulatory Excellence with ShionogiAt Shionogi, we are dedicated to protecting the health and well-being of people worldwide. As a global pharmaceutical leader, we are driven by science, innovation, and a deep sense of responsibility to public health. Join us in our mission to deliver life-changing treatments by ensuring robust...
-
Regulatory Affairs Associate
1 day ago
London, Greater London, United Kingdom WEP Clinical Full time £40,000 - £70,000 per yearAre you seeking an exciting and fulfilling new opportunity? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring forward ideas that make a real difference. Be part of a...
-
Associate Director, Regulatory Affairs
2 weeks ago
London, Greater London, United Kingdom Novartis Full time £80,000 - £120,000 per yearJob Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks), United KingdomThe Associate Director, Regulatory Affairs (Medical Devices) independently provides strategic and operational global medical device regulatory direction and documentation for projects/products covering design and development, registration, approval...
-
Regulatory Affairs Associate
7 days ago
London, Greater London, United Kingdom Dechra Full time £36,325 - £40,075 per yearSummaryThanks for checking out our vacancy, we're delighted you want to learn more about DechraDechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.Here at Dechra, our values are embedded...
-
Global Regulatory Affairs Associate Director
2 weeks ago
London, Greater London, United Kingdom Novartis Full time £80,000 - £120,000 per yearJob Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks), United Kingdom or Dublin, IrelandWe are looking for an experienced and proactive Global Regulatory Affairs Associate Director Cardio-Metabolic to join our Global Regulatory Affairs team.The role involves directing the development and submission of regulatory...
-
Regulatory Affairs Lead
3 days ago
London, Greater London, United Kingdom Our Future Health Full time £70,000 - £100,000 per yearWe have an exciting opportunity for a Regulatory Affairs Lead to join our Ethics, Compliance and Governance department. This role is vital to Our Future Health's ability to deliver participant feedback and recontact studies within a complex regulatory environment. It ensures Our Future Health remains credible with external regulators and able to make timely,...
-
Regulatory Affairs Lead
3 days ago
London, Greater London, United Kingdom Our Future Health UK Full time £70,000 per yearWe have an exciting opportunity for a Regulatory Affairs Lead to join our Ethics, Compliance and Governance department. This role is vital to Our Future Health's ability to deliver participant feedback and recontact studies within a complex regulatory environment. It ensures Our Future Health remains credible with external regulators and able to make timely,...
-
Senior Director, Regulatory Affairs
5 days ago
London, Greater London, United Kingdom Beacon Therapeutics (USA) Inc Full time £150,000 - £200,000 per yearJoin Beacon Therapeutics (USA) Inc. as a Full-Time Senior Director of Regulatory Affairs and be at the forefront of transformative biotech innovations. This is a unique opportunity to shape regulatory strategies that directly influence the success of groundbreaking therapeutics in the UK market. Here, you will have the chance to leverage your expertise in a...
-
Senior Director, Regulatory Affairs
4 days ago
London, Greater London, United Kingdom Beacon Therapeutics Full time £120,000 - £200,000 per yearJoin Beacon Therapeutics (USA) Inc. as a Full-Time Senior Director of Regulatory Affairs and be at the forefront of transformative biotech innovations. This is a unique opportunity to shape regulatory strategies that directly influence the success of groundbreaking therapeutics in the UK market. Here, you will have the chance to leverage your expertise in a...
-
Regulatory Affairs Specialist
5 days ago
London, Greater London, United Kingdom Sava Full time £60,000 - £120,000 per yearAbout SAVAAll the health information we need is within us. Just below the skin. SAVA is redefining the way people interact with their health by developing the most advanced biosensing technology science has to offer, capable of accessing bodily information in a painless, real-time and affordable way.The RoleAt SAVA, we are building next-generation biosensors...