Senior Manager Medical Writing and Regulatory Affairs

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 looking for a seasoned professional to lead our Medical Writing and Regulatory Affairs department at Barrington James, a pioneering firm in the clinical trials sector. In this critical role, you will oversee the preparation and delivery of high-quality regulatory submissions and medical writing outputs.Job Details:This senior leadership position...

Regulatory Affairs and Content StrategyAs the Medical Writing and Regulatory Affairs Director, you will be responsible for leading our medical writing team and developing strategic content initiatives to drive business growth.ResponsibilitiesDevelop and implement a content strategy that aligns with our business objectives.Collaborate with cross-functional...

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...

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...

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...

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...

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...

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...

Richmond Pharmacology, a leading Contract Research Organisation (CRO), is seeking an experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing and regulatory teams. As a senior leader, you will oversee the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy, and...

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...

Barrington James is a prominent organisation within the clinical trials sector, focusing on early-phase studies for pharmaceutical and biotechnology clients. We are seeking a talented and experienced Head of Medical Writing and Regulatory Submissions to lead our medical writing team in advancing medical innovation and supporting the development of...

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 OverviewWelcome to Warman O'Brien, a leading pharmaceutical company seeking an experienced Senior Regulatory Affairs Director to lead our medical writing team.This is a hybrid role in Central London, requiring applicants to be prepared to work on-site four days per week.As the Head of Medical Writing and Regulatory Affairs, you will provide...

Richmond Pharmacology, a leading Contract Research Organisation (CRO), seeks an experienced Senior Regulatory Affairs Specialist to oversee medical writing and regulatory submissions.Estimated salary: £80,000 - £110,000 per annum.We are committed to excellence and innovation in early-phase clinical trials for pharmaceutical and biotechnology sponsors. Our...

Become an integral part of Barrington James, a leading player in the clinical trials sector, as our new Medical Writing and Regulatory Director. In this role, you will be responsible for overseeing medical writing and regulatory submissions, ensuring compliance with all relevant regulations.About the Role:Lead a team of medical writers 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 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...

Unlock Your Potential as a Senior Medical Writing Lead at Barrington JamesWe are seeking an accomplished Senior Medical Writing Lead to join our dynamic team at Barrington James. This exciting opportunity offers the chance to lead and manage teams within a fast-paced, research-driven environment dedicated to advancing medical innovation.About the Role:As...

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...