📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...
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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...
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📑 Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunit ...
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📑 As a Senior Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As a Senior Medical Writer you will be supporting a Top-5 pharma company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. While ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Job Title: Regulatory Affairs – Senior CMC Dossier ManagerJob Type: Contract position until December 2024, inside IR35Rate: Up to £85ph PAYE or UmbrellaLocation: UK or Europe (Remote-based)CPL has partnered with a world-leading Biotech looking for an experienced Regulatory CMC leader to work on a developing rare disease portfolio. This will be supp ...
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📑 Newly created role for an experienced Bid Writer / Manager to join an established bid team within the highways sector.The Senior Bid Writer / Manager is primarily responsible for supporting the Bid Team in the bespoke content development and management of tender opportunities. Managing individual bids from initial decision through to final submissi ...
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📑 Newly created role for an experienced Bid Writer / Manager to join an established bid team within the highways sector.The Senior Bid Writer / Manager is primarily responsible for supporting the Bid Team in the bespoke content development and management of tender opportunities. Managing individual bids from initial decision through to final submissi ...
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📑 The Role The Senior Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas. Plan and deliver regulatory submissions on behalf of pharmaceutical clients Prepare clinical regulatory documents across multiple therapy areas Evaluate scientific data Work on proj ...
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📑 Senior Medical Writer - Global Med Comms Agency - Remote, UKPhenomenally excited to be partnering with my Global Med Comms Agency client to support them in their search for a Senior Medical Writer to join thriving their UK team.We are looking for a Senior Medical Writer, ideally from a Med Comms background, who has been exposed to working on Public ...
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📑 Senior Medical Writer - Global Med Comms Agency - Remote, UKPhenomenally excited to be partnering with my Global Med Comms Agency client to support them in their search for a Senior Medical Writer to join thriving their UK team.We are looking for a Senior Medical Writer, ideally from a Med Comms background, who has been exposed to working on Public ...
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📑 Principal Medical Writer (EMEA) (FSP; Remote) At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resour ...
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📑 Are you a seasoned SOP writer with a knack for navigating the intricacies of Good Manufacturing Practices (GMP) and commercial product standards? If so, we have an exciting opportunity for you!We are on the lookout for a highly skilled Interim SOP Writer to join a dynamic team on a fully remote basis for a minimum 3-month contract. As an SO ...
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📑 Are you a seasoned Senior Medical Writer with a passion for scientific publications, client interaction, and communicating complex scientific messages? Want to take the next step in your career and be part of a dynamic and supportive environment where your contributions make a difference?This Senior Medical Writer role with a focus on oncology publ ...
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📑 Are you a seasoned Senior Medical Writer with a passion for scientific publications, client interaction, and communicating complex scientific messages? Want to take the next step in your career and be part of a dynamic and supportive environment where your contributions make a difference?This Senior Medical Writer role with a focus on oncology publ ...
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📑 The Role The Senior Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas. Plan and deliver regulatory submissions on behalf of pharmaceutical clients Prepare clinical regulatory documents across multiple therapy area ...
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📑 Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and ...
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📑 The Role The Senior Medical Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research. Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc Managing multiple projects Reviewing all documentation to a high standard You To ap ...
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📑 Newly created role for an experienced Bid Writer / Manager to join an established bid team within the highways sector.The Senior Bid Writer / Manager is primarily responsible for supporting the Bid Team in the bespoke content development and management of tender opportunities. Managing individual bids from initial decision through to final ...
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📑 Are you a seasoned Senior Medical Writer with a passion for scientific publications, client interaction, and team leadership? Want to take the next step in your career and be part of a dynamic and supportive environment where your contributions make a difference? This Principal Medical Writer role with a focus on oncology publications could just be ...
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📑 Are you a seasoned Senior Medical Writer with a passion for scientific publications, client interaction, and team leadership? Want to take the next step in your career and be part of a dynamic and supportive environment where your contributions make a difference? This Principal Medical Writer role with a focus on oncology publications could just be ...
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📑 The Role The Senior Medical Writer - Regulatory/Clinical will be responsible for researching, creating and editing all documents associated with clinical research. Writing Clinical Study Reports, Protocols, Informed Consent to Clinical Overviews etc Managing multiple projects Reviewing all ...
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📑 Reports to Principal Medical Writer or Scientific Team Lead MSSJob summaryAs a Senior Medical Writer, you will play a pivotal role in shaping the communication of complex scientific ideas. Taking leadership of large projects/specific workstreams across a range of medical communications deliverables, you will be responsible f ...
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📑 Reports to Principal Medical Writer or Scientific Team Lead MSSJob summaryAs a Senior Medical Writer, you will play a pivotal role in shaping the communication of complex scientific ideas. Taking leadership of large projects/specific workstreams across a range of medical communications deliverables, you will be responsible f ...
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📑 As a Principal Medical Writer you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. As principal medical writer, you will be supporting a Top-5 biotech company. You have the chance to help our customer to deliver best-in-class regulatory and submission documents. ...
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📑 Senior Medical Writer - Publications Are you a seasoned Medical Writer looking to take the next step in your career? We have an exceptional opportunity available at a leading company in the medical communications industry.We're seeking a talented Senior Medical Writer to join an esteemed team, where you'll have the chance to expand your expertise a ...
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📑 Senior Medical Writer - Publications Are you a seasoned Medical Writer looking to take the next step in your career? We have an exceptional opportunity available at a leading company in the medical communications industry.We're seeking a talented Senior Medical Writer to join an esteemed team, where you'll have the chance to expand your expertise a ...
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📑 The Role Working on a number of exciting projects and with an exciting pipeline, the Principal Medical Writer (Regulatory / Clinical) will be responsible for; Writing, editing, and reviewing documents such as Clinical Study Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Nar ...
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📑 Tax Writer / Tutor Do you enjoy a rigorous technical and intellectual challenge? About our Team LexisNexis Legal & Professional, which serves customers in more than 150 countries with 11,300 employees worldwide, is part of RELX, a global provider of information-based analytics and decision tools for pro ...
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📑 At Cancer Research UK, we exist to beat cancer . We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That’s why we we’re looking for someone talented, someone innovative and ambitious, someone like you. About the team The Cancer Research ...
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📑 Tax Writer / TutorDo you enjoy a rigorous technical and intellectual challenge?About our TeamLexisNexis Legal & Professional, which serves customers in more than 150 countries with 11,300 employ ...
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📑 If you are looking for your next career move as a SENIOR MEDICAL WRITER then we would love to talk to you.As a Senior Medical Writer you will need to produce high quality educational materials for the pharmaceutical industry to enhance understanding of the disease and treatment; helping clients communicate their educational objectives to relevant a ...
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📑 If you are looking for your next career move as a SENIOR MEDICAL WRITER then we would love to talk to you.As a Senior Medical Writer you will need to produce high quality educational materials for the pharmaceutical industry to enhance understanding of the disease and treatment; helping clients communicate their educational objectives to relevant a ...
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📑 Our client is looking for a Senior Medical Writer to lead and work across a wide range of projectsThe client are a vibrant global healthcare communications agency with a geographical footprint in Europe and North America. By coupling excellent scientific expertise with intelligent creativity, they deliver meaningful solutions through an agi ...
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📑 Our client is looking for a Senior Medical Writer to lead and work across a wide range of projectsThe client are a vibrant global healthcare communications agency with a geographical footprint in Europe and North America. By coupling excellent scientific expertise with intelligent creativity, they deliver meaningful solutions through an a ...
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📑 **Job Description** **Principal Medical Writer (EMEA) (FSP; Remote)** At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We pr ...
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📑 The Role Working on a number of exciting projects and with an exciting pipeline, the Senior Medical Writer (Regulatory) will be responsible for; Writing, editing, and reviewing documents such as Clinical Study Report, Protocols, Informed Consent, Safety Aggregate Reports (DSUR/PBRER), Safety Narratives, Clini ...
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📑 **Job Description** **Senior Medical Writer (EMEA) (FSP; Remote)** At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provi ...
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📑 Real Chemistry is a global health innovation company with offices across Europe and the US. We believe that the way to real, transformative change is through the uncommon combination of disciplines, technologies, and our greatest asset – our people. We are currently looking to add to our alchemic mix of more than 1,800 talented professionals. This ...
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📑 Real Chemistry is a global health innovation company with offices across Europe and the US. We believe that the way to real, transformative change is through the uncommon combination of disciplines, technologies, and our greatest asset – our people. We are currently looking to add to our alchemic mix of more than 1,800 talented professionals. This ...
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📑 Real Chemistry is a global health innovation company with offices across Europe and the US. We believe that the way to real, transformative change is through the uncommon combination of disciplines, technologies, and our greatest asset – our people. We are currently looking to add to our alchemic mix of more than 1,800 talented professionals. This ...
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📑 Real Chemistry is a global health innovation company with offices across Europe and the US. We believe that the way to real, transformative change is through the uncommon combination of disciplines, technologies, and our greatest asset – our people. We are currently looking to add to our alchemic mix of more than 1,800 talented professionals. This ...
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📑 Reports to Principal Medical Writer or Scientific Team Lead MSSJob summaryAs a Senior Medical Writer, you will play a pivotal role in shaping the communication of complex scientific ideas. Taking leadership of large projects/specific workstreams across a range of medical communications deliverables, you will be res ...
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📑 Reports to Principal Medical Writer or Scientific Team Lead MSSJob summaryAs a Senior Medical Writer, you will play a pivotal role in shaping the communication of complex scientific ideas. Taking leadership of large projects/specific workstreams across a range of medical communications deliverables, you will be res ...
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📑 Reports to Medical Writer/Senior Medical WriterJob SummaryThis is a great opportunity to enter the world of medical communications! A Life Sciences degree and a passion for healthcare is a good starting point, no previous writing experience is necessary.Essential Duties & Responsibilities Ensuring that ...
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📑 My client is a dynamic and expanding global asset manager who has had excellent performance throughout the last few years. We are hiring a brand new role to the business and seeking an accomplished Senior RFP Writer with a strong background in Fixed Income to act as a number two to the Global Head of RFP.This is an exciting opportunity to join an e ...
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📑 My client is a dynamic and expanding global asset manager who has had excellent performance throughout the last few years. We are hiring a brand new role to the business and seeking an accomplished Senior RFP Writer with a strong background in Fixed Income to act as a number two to the Global Head of RFP.This is an exciting opportunity to join an e ...
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📑 Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and ...
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📑 The Role The Principal Regulatory Writer will be responsible for leading the planning and delivery of regulatory submissions and other large regulatory projects in a concise and accurate manner. Plan and deliver regulatory submissions on behalf of pharmaceutical clients Prepare clinical regulatory documents across multiple therapy areas E ...
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📑 The Role The Regulatory Writer will have the opportunity to work with well known, innovative pharmaceutical companies across a range of therapy areas. Plan and deliver regulatory submissions on behalf of pharmaceutical clients Prepare clinical regulatory documents across multiple therapy areas Evaluate scientific data Work on projects in ...
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