Regulatory Affairs and Medical Writing Director

OverviewWe are seeking a highly skilled Regulatory Affairs Manager to join our team at the Regulatory Affairs Professionals Society. As a key member of our organization, you will be responsible for overseeing regulatory strategy and ensuring compliance within our ingredient agent, brokerage, and solution manufacturing businesses.

Overview:Richmond Pharmacology, a leading Contract Research Organisation (CRO), is seeking an experienced Head of Medical Writing and Regulatory Submissions to lead and develop our medical writing and regulatory teams.Salary: Competitive Salary + Benefits (£80,000 - £100,000)About the Role:We are looking for a skilled professional to oversee the...

About the RoleWe are seeking a Medical Writing and Regulatory Affairs Lead to join our dynamic team at Barrington James.In this role, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs, ensuring adherence to all relevant regulatory standards.The ideal candidate will have a...

We are seeking an experienced professional to lead our medical writing and regulatory teams. As a Senior Director, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and compliance with regulatory standards.Job Description:Manage the entire medical writing and regulatory...

About Richmond Pharmacology:We are a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and contribute to the development of life-changing therapies.Location: London Bridge (Hybrid 4 Days...

Senior Medical Writing and Regulatory Submissions RoleWe are seeking an accomplished professional to lead our medical writing and regulatory teams. As the Head of Medical Writing and Regulatory Submissions, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables.This senior role involves strategic guidance on...

Job SummaryWe are seeking a highly skilled and experienced Head of Medical Writing and Regulatory to lead our team in delivering high-quality regulatory submissions and medical writing outputs.The ideal candidate will have a strong background in medical writing and regulatory submissions, with experience in managing teams and ensuring compliance with...

Job DescriptionThe successful candidate will be a strategic leader with expertise in medical writing and regulatory affairs. They will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy and compliance with regulatory standards. This role requires strong leadership skills, including the...

MCRA, a leading medical device advisory firm and clinical research organization (CRO), offers an exciting opportunity for a Manager, Regulatory Affairs. Based in Europe, this critical team member will support regulatory strategy and submissions for clients across various therapeutic areas.As a key player in our regulatory team, you will be responsible for...

Key ResponsibilitiesTaking full accountability of all medical writing and regulatory activitiesDirecting line management responsibilities for the Medical Writing team, with two employees under your managementProviding regulatory expertise to project teams on all aspects of the clinical trials processSupporting the organisation and preparation of regulatory...

Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. We are seeking an experienced medical writing and regulatory expert to join our team as Senior Director of Medical Content and Compliance.Key Responsibilities:Oversee the preparation and submission...

Job Title: Head of Medical Writing and Regulatory SubmissionsA leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.Position Overview:We are hiring a...

Job OverviewWe are seeking an experienced Clinical Director to lead our medical writing and regulatory submissions teams at Lifelancer, a talent-hiring platform in Life Sciences. As a key member of our team, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and compliance...

Role Overview:Barrington James is seeking an exceptional Senior Medical Writing and Regulatory Submissions Specialist to lead our Medical Writing and Regulatory Affairs department. As a key member of our team, you will be responsible for overseeing the preparation and delivery of high-quality regulatory submissions and medical writing outputs, ensuring...

The Association of International Certified Professional Accountants is seeking a talented Regulatory Affairs Director to lead our compliance initiatives. This is an excellent opportunity for a professional with a strong background in regulatory affairs to take on a leadership role and contribute to our organization's growth.About the Company: We operate...

Job DescriptionBarrington James is seeking a seasoned professional to fill the role of Head of Medical Writing and Regulatory Submissions. This senior leadership position offers a unique opportunity to lead and manage teams in a dynamic research-driven environment.The ideal candidate will have a strong background in medical writing and regulatory...

About the RoleA leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors seeks to advance medical research and support the development of transformative therapies through excellence and innovation.With a competitive salary package of £70,000+ per annum, this senior-level position...

Job SummaryThe Director of Regulatory Affairs and Content Strategy will provide senior level expertise and management for our client's medical writing team at Warman O'Brien.This is a hybrid role in Central London, requiring the successful candidate to work on-site 4 days per week. The ideal candidate will have significant experience authoring pharmaceutical...

Arevna is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials. We are currently seeking a Senior Regulatory Affairs Manager to lead our regulatory affairs team in Central London.Job Description:The successful candidate will be responsible for driving the development and commercialisation of our Medical Writing and...

ICON plc is a leading healthcare intelligence and clinical research organization seeking an experienced Regulatory Affairs Director to join our team. This role plays a pivotal part in designing and analyzing clinical trials, interpreting complex medical data, and advancing innovative treatments.Key Responsibilities:Lead regulatory operations activities...