Regulatory Writing Consultant

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners...

Proclinical are recruiting a Regulatory CMC Consultant for a pharmaceutical organisation. This role is on a contract basis and is located in West London. **Responsibilities**: - Accountable for highlighting possible delaying factors promptly to line management as well as share knowledge of regulatory documentation and processes with others. - You will...

Role Summary With an expanding regulatory team, an exciting opportunity has arisen for an Associate Director or a Director to join the Autolus Regulatory and Medical Writing team to support global expansion of our cell and gene therapy products. This position requires a medical writing professional with a proven track record of successfully working as a...

As an Equifax Consultant, you will play a pivotal role in the Client Analytics team within Data and Analytics (D&A). You will work closely with clients to proactively understand their challenges, propose and develop solutions and lead the execution of analytical and consultancy projects, including the design and development of complex modelling assignments...

Medical Education Writer – Senior medical education agency – Bucks The editorial and medical writing team, at this Buckinghamshire medical education agency, is the largest team of its kind among similar mid-size agencies. This means that, as Senior Medical Writer, you benefit from excellent personal development opportunities – both through the...

Medical Education Writer – Senior medical education agency – Bucks The editorial and medical writing team, at this Buckinghamshire medical education agency, is the largest team of its kind among similar mid-size agencies. This means that, as Senior Medical Writer, you benefit from excellent personal development opportunities – both through the...

Join Our Pioneering Regulatory Consulting Team as a Consultant! DWF is a global legal business providing high quality legal services across legal advice and managed services. At DWF, we're expanding our Regulatory Consulting team and looking for a Consultant to help shape the future of regulatory strategies. Step into the world of DWF's Regulatory...

Join Our Pioneering Regulatory Consulting Team as a Consultant! DWF is a global legal business providing high quality legal services across legal advice and managed services. At DWF, we're expanding our Regulatory Consulting team and looking for a Consultant to help shape the future of regulatory strategies. Step into the world of DWF's Regulatory...

Looking for a remote position and the ability to impact several clients? Look no further. Adecco is working with a highly successful consultancy who are hiring a Regulatory Consultant to join the team on a permanent basis. The business runs several projects concurrently, so depending on your skill set, you will take ownership in supporting manufacturing...

BaxMed – Ad-Hoc Senior Regulatory Affairs Consultant Led by Stuart Baxter, a seasoned professional with a distinguished career in Regulatory Affairs, BaxMed Regulatory Ltd is an exciting early-stage organisation formed to provide Regulatory and Quality Compliance Services for the global Medical Device / healthcare sector. With a core ethos and commitment...

Job Description InterQuest are currently supporting a leading specialist consultancy in finding a talented compliance consultant to support the growth of their Investments division. As a regulatory expert in the space, this would be a great opportunity for leverage your consultancy expertise and take the next step in your career in what is a...

InterQuest are currently supporting a leading specialist consultancy in finding a talented compliance consultant to support the growth of their Investments division. As a regulatory expert in the space, this would be a great opportunity for leverage your consultancy expertise and take the next step in your career in what is a culture-orientated business...

Regulatory Affairs Consultant CMC, biologics outside of IR35Your new companyThis growing US rare disease company is looking for an experienced Regulatory Affairs CMC (biologics) professional to join them on a 12-month contract, this contract job is outside of IR35 and can be fully remote or hybrid working.Your new roleAs Regulatory Affairs Consultant CMC,...

Job Description Our client, a global Investment Manager, is looking to bring a Regulatory Compliance Consultant onboard for an initial 6-month contract as soon as possible. The role is paying around £550 per day PAYE and requires the consultant to be based in the London office, 5-days a week. Enhance, draft, and maintain policies, procedures, and other...

Division Overview Customer Services is an integral part of Adenza's growth and success. This division's mission is to continuously enhance the Adenza Customer experience in how they consume the Adenza software and services, using a strategic customer-centric approach focused on driving customer adoption and retention. Thus, successfully differentiating...

Quality Consultant - Project Camberley/ Hybrid 12 month contract CPL Life sciences are currently recruiting a quality consultant to fulfil a 12 month contract. The perfect candidate will ensure compliant and efficient execution of the quality project across the UK and Ireland organisations. You will need to have extensive experience in the...

Regulatory Affairs Consultant. 8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Lead and / or...

Regulatory Affairs Consultant. 8+ years' experience in handling life cycle management of approved drug products (like- tablets (oral solids), syrups (oral liquids), parenterals (injections/ injectables for EU market. Good understanding of regulatory framework, including regional trends, for various types of applications and procedures Lead and / or...

  Key Responsibilities: Act as the key point of contact for the wider business within the EMEA region Partner with internal departments globally to identify and mitigate potential regulatory risks in the cryptocurrency space Stay current on the ever-evolving regulatory landscape in the EMEA region Develop and maintain comprehensive procedures for...