Regulatory Affairs and Clinical Manager

An opportunity for a Chemical Regulatory Affairs Specialist to join a global chemical trade association as manager of global regulatory intelligence. You will be responsible for: Regulatory horizon scanningTracking and analysing updates and changes to global chemical regulationsAssessing the impact on members substances Working with a range of stakeholders...

Associate Director Regulatory AffairsRemote Competitive salary + bonus + car allowance + shares/stocks Reporting to the Vice President of Regulatory Affairs, the Associate Director of Regulatory Affairs is responsible for providing regulatory oversight and support for both the operational and supervised strategic regulatory activities for, selected global...

Senior Regulatory Affairs Specialist to work at Corin, you will be responsible for product registration and all regulatory aspects of post-market surveillance. The Senior Regulatory Affairs Specialist will require extensive knowledge of all applicable standards, regulations, and guidance to support pre- and post-market requirements, as well as the ability to...

CK Group are recruiting for a Regulatory Affairs Manager to join a biopharmaceutical company who are based in Cambridge on a contract basis for 12 months.Company:Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics....

Role: Regulatory Affairs Associate Manager - Cosmetics Location: Home-based anywhere in the UKJob Type: 6+ Month contractSalary / Rate: Very competitive hourly ratePlanet Pharma are partnered with a niche mid-sized CRO assisting them with the search for an Associate Manager, Regulatory Affairs to work on an initial 6+ month project with a focus on Cosmetic...

Director Global Regulatory AffairsBOUT THE ROLEThe Director, Global Regulatory Affairs will be responsible for developing, implementing and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives.Global Regulatory Affairs is expected to:• Provide high level...

Experienced in Chemical Regulatory Affairs? Want to experience working within the Trade Association field in a sector which is crucial in today's industry?We are collaborating with a prominent global trade association that focuses on promoting the responsible and sustainable production and utilization of metals. Their efforts are vital in today's...

Location – Remote, MacclesfieldOutside IR35Duration – 6 monthsMake a meaningful difference at AstraZeneca!Bring out the best in each other, and yourself, by working together as one.When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working give us the platform we need to...

Director of Regulatory Affairs:Are you highly strategic regulatory leader with executive stakeholder management experience, adept at reshaping relationships with external stakeholders and leading your teams through periods of change and transformation? We're seeking a Director of Regulatory Affairs to join our senior leadership team, reporting to and...

Director of Regulatory AffairsWalker Cole International are delighted to be partnering with a large IVD multinational, who are looking to hire a Director of Regulatory Affairs. This is a fully remote position that requires up to 20% travel. The successful candidate will lead a dynamic team, oversee all regulatory activities, and be responsible for the...

Regulatory affairs CMC ConsultantRemote Tasks & Responsibilities: Provide advice to clients on quality aspects of drug development and regulatory requirements, in close collaboration with cross-functional experts from the teamEnsure that the content of CMC work-packages and documentation are phase appropriate, meet regulatory expectations and enable approval...

Austin Vita are delighted to be offering a fully remote, permanent, job opportunity for an experienced Medical Device Regulatory Affairs professional to join a well established Regulatory Group as a Team Leader working on Class III Devices for a global manufacturer.Responsibiliites:Preparation and review of regulatory documentation and submissions for...

Job Title: Associate Director of Clinical Operations Company Overview: Our client is a dynamic and innovative small biotech company dedicated to advancing breakthrough therapies in cell and gene therapy. We pride ourselves on our commitment to pushing the boundaries of medical science to improve patient outcomes. As we continue to grow, we are seeking a...

ProPharma Group is the leading global, independent, single-source provider of regulatory, clinical, and compliance services serving pharmaceutical, biotechnology, and medical device companies. Our team of experts brings a comprehensive portfolio of regulatory sciences, clinical research solutions, life science consulting, R&D technology, pharmacovigilance,...

Job Title: Clinical Statistician, Data ScienceLocation: United Kingdom (Remote)Type: Full-time, PermanentResponsibilities:• Contributes to parts of the planning, execution and reporting of clinical/observational studies including post hoc, HTA, regional, PK-PD or Biomarkers analyses in collaboration with the Study Statistician.• Is responsible for the...

Remote Clinical Editor working through an FSP model for a Global Oncology focused Pharmaceutical CompanyThe Clinical Editor is responsible for ensuring the quality of clinical documents intended for submission to health authorities worldwide. The Clinical Editor will review clinical documents for grammar, style, and formatting to ensure compliance with...

Remote Senior Regulatory Medical Writer working through an FSP model for a Global Oncology focused Pharmaceutical CompanyThe Principal Medical Writer I is responsible for developing clinical documents for submissions to regulatory authorities globally.Provides strategic direction to cross-functional project teams with minimal oversight to ensure that...

An exceptional opportunity awaits with our client, a dynamic Regulatory Affairs Consultancy with a presence in the UK, Switzerland, and Ireland, serving global clients. In this role, you will join a team of seasoned experts in Regulatory, CMC, Clinical, and Non-Clinical fields, leveraging your CMC and Regulatory expertise to provide comprehensive support and...

External Affairs AssistantFinance Membership Body 2.5 Days Office, Central London, 2.5 Days HomeBasic Salary Up to £30,000 dependant on experience with excellent benefits including 26 days Holiday, Pension Scheme, Health Insurance, Life Assurance 4 x annual salary and BUPA for self and partner. Permanent, Full TimeOur client a finance membership body is...

About the roleWe are seeking dedicated clinical professionals with a fervor for innovation and adept problem-solving skills to bolster our team in spearheading clinical research development endeavors in the United Kingdom. As a Clinical Research Data Analyst, you will play a pivotal role revolves around ensuring the seamless delivery of therapeutic...