Sr / Regulatory Medical Writer - Certain Emea
il y a 1 semaine
At Thermo Fisher Scientific, you’ll 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 resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
**Sr / Medical Writer, Regulatory**
**(remote from certain EMEA locations)**
As part of our on-going growth, we are currently recruiting for a Senior / Medical Writer to join our rapidly expanding team of over 170 regulatory writers based in Europe, North America and Asia Pacific.
Our writers possess strong leadership and project management skills, are creative problem solvers and decision makers, are engaging mentors and enthusiastic members of the department with an eagerness to continually improve our offerings and deliver a market leading service to our clients. In return, the medical writing department offers a highly competitive compensation package together with excellent opportunities for personal development and progression within the field. All within a friendly, fast paced and exciting environment.
The Medical Writer collaborates with internal and sponsor team members to interpret, distill, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarization of preclinical and clinical studies for preparation of investigator's brochures, and referencing current research and regulatory guidelines for preparation of protocols. Their work documenting clinical study trials covers a wide range of therapeutic indications.
You will be a part of a team who is dedicated to its people and foster a supportive, collaborative culture based on trust, flexibility and work life balance.
**Qualifications required**:
- Education to Bachelor’s/advanced degree level in a scientific discipline
- 3 to 5+ years of experience within regulatory medical writing. We are hiring Medical Writers and Sr Medical Writers.
- Excellent grammatical, editorial and proofreading skills
**Our 4i Values**:
**Integrity - Innovation - Intensity - Involvement
-
Sr / Regulatory Medical Writer - Certain Emea
il y a 4 semaines
Brussels, Belgique Thermo Fisher Scientific Temps pleinAt Thermo Fisher Scientific, you’ll 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 resources needed to achieve individual career goals while taking science a step beyond through...
-
Program Manager Medical Writing
il y a 6 jours
Brussels, Belgique Thermo Fisher Scientific Temps pleinAt Thermo Fisher Scientific, you’ll 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 resources needed to achieve individual career goals while taking science a step beyond through...
-
Medical Writer
il y a 6 jours
Brussels, Belgique Jefferson Wells Temps pleinLocation: **BRUSSEL** - Type: **Contracting** **#19752** Will you be our new ambassador? **Jefferson Wells Life Sciences** specializes in supporting **pharma & biotech companies** in their daily challenges. Hence our interest in **experts** like you to pass our team. Let's look together at your first challenge with us! **Medical Writer** **Scope of...
-
Sr Manager, Regional Category Management, Surgical Emea
il y a 2 jours
Brussels, Belgique Ansell Temps plein**Sr Manager, Regional Category Management, Surgical EMEA** **-** **(**30010127**)** **Description** **Why Ansell?** Ansell is looking for a **Sr Manager, Regional Category Management, Surgical EMEA** to join our team in **Brussels, BE or Krakow, PL.** In this position you will play a vital role in overseeing brand and product management activities,...
-
Lead Regulatory Counsel, Emea
il y a 3 semaines
Brussels, Belgique Facebook App Temps pleinSupervise and direct outside counsel on multiple regulatory litigation matters across EMEA - Help to inform and execute litigation strategy in relation to matters pending before national and international courts - Work with cross-functional teams on data protection, public policy, platform/partnership, product, privacy, and commercial issues Develop creative...
-
Regulatory Litigation Counsel, Emea Disputes
il y a 2 jours
Brussels, Belgique Meta Temps pleinMeta seeks a highly motivated lawyer to join Meta’s EMEA Disputes Regulatory team. You will work within the EMEA wide regulatory litigation team on high-profile, precedent-setting regulatory investigations and related litigation in the European courts focusing on privacy laws, artificial intelligence, and other emerging technology-related laws in Europe....
-
Junior Medical Writer
il y a 6 jours
Brussels, Belgique Oxford Global Resources Temps pleinAs a Medical Writer, you will be working on the writing of scientific tender dossiers for which you will be working in tandem with a Tender manager. The focus will be on Clinical documents and/or publications (articles, abstracts, summaries etc.) or other documents. **Responsibilities** - Writing scientific tender dossiers in tandem with a Tender Manager. -...
-
Regulatory Submission Planner
il y a 2 semaines
Brussels, Belgique MSD Temps pleinWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for...
-
Regulatory Submission Planner
il y a 7 jours
Brussels, Belgique MSD Temps pleinWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for...
-
Lead Counsel, Emea Content
il y a 3 semaines
Brussels, Belgique Facebook App Temps plein**Lead Counsel, EMEA Content & Disputes Responsibilities**: - Manage complex regulatory investigations, regulatory litigation and other matters across EMEA, with a focus on content regulation - Guide and execute regulatory and litigation strategy in relation to high-profile, precedent setting matters with the potential for reaching the highest appellate...
-
Clinical Program Manager
il y a 1 semaine
Brussels, Belgique Inari Medical Temps plein**Description** The Clinical Research Program Manager is responsible for leading all aspects of clinical trial management across the study life-cycle from planning to execution to closure. They work with cross functional partners or Contract Research Organizations to collect and deliver high quality evidence, enabling patient access to advanced care of their...
-
Regulatory Litigation Counsel
il y a 1 semaine
Brussels, Belgique Meta Temps plein**Regulatory Litigation Counsel Responsibilities**: - Engage and collaborate with outside counsel on multiple regulatory and litigation matters across EMEA. - Provide legal advice and assist in managing various stages of regulatory inquiries and consequent litigation in relation to matters pending before national regulators, as well as national and...
-
Sr. Director, International Government Affairs
il y a 4 semaines
Brussels, Belgique Axon Temps plein**Join Axon and be a Force for Good.**: At Axon, we're on a mission to Protect Life. We're explorers, pursuing society's most critical safety and justice issues with our ecosystem of devices and cloud software. Like our products, we work better together. We connect with candor and care, seeking out diverse perspectives from our customers, communities and...
-
Regulatory Litigation Counsel
il y a 1 semaine
Brussels, Belgique Facebook App Temps plein**Regulatory Litigation Counsel Responsibilities**: - Engage and collaborate with outside counsel on multiple regulatory and litigation matters across EMEA. - Provide legal advice and assist in managing various stages of regulatory inquiries and consequent litigation in relation to matters pending before national regulators, as well as national and...
-
EMEA Demand
il y a 3 semaines
Brussels Metropolitan Area, Belgique MountainTop Life-Sciences Temps pleinOur client, a global leader in medical device manufacturing, is seeking a Demand & Supply Planner to support EMEA-wide forecasting and inventory management. This role is crucial in ensuring optimal product availability while maintaining supply chain efficiency.Key Responsibilities:Develop accurate demand forecasts for key medical device products across...
-
Medical Writer
il y a 3 semaines
Brussels, Belgique Jefferson Wells Temps pleinLocation: **Brussels** Type: **Contracting** **#17242** Will you be our new ambassador? **Jefferson Wells Life Sciences** specializes in supporting **pharma & biotech companies** in their daily challenges. Hence our interest in **experts** like you to pass our team. Let's look together at your first challenge with us! The tasks will be limited to Medical...
-
Regulatory Counsel
il y a 1 semaine
Brussels, Belgique Bandwidth Temps plein**Who We Are**: At Bandwidth, your music matters when you are part of the BAND. We celebrate differences and encourage BANDmates to be their authentic selves. #jointheband **What We Are Looking For**: We are looking for a Regulatory Counsel to come and join our International Regulatory team, based in Brussels as we continue with exciting projects,...
-
Planning Lead Emea
il y a 4 semaines
Brussels, Belgique Terumo Temps pleinPlanning Lead EMEA **Date**:Jan 17, 2025 **Location**: Brussels, BE **Company**:Terumo BCT, Inc. **Requisition ID**: 33271 At Terumo Blood and Cell Technologies, our 7,000+ global associates are proud to come to work each day, knowing that what we do impacts the lives of patients around the world. We make medical devices and related products that are...
-
Planning Lead Emea
il y a 2 jours
Brussels, Belgique Terumo Temps pleinPlanning Lead EMEA **Date**:Jan 17, 2025 **Location**: Brussels, BE **Company**:Terumo BCT, Inc. **Requisition ID**: 33271 At Terumo Blood and Cell Technologies, our 7,000+ global associates are proud to come to work each day, knowing that what we do impacts the lives of patients around the world. We make medical devices and related products that are...
-
Regulatory Litigation Counsel
il y a 3 jours
Brussels, Belgique Meta Temps plein**Regulatory Litigation Counsel Responsibilities**: - Engage and collaborate with outside counsel on multiple regulatory and litigation matters in Ireland and across EMEA. - Provide legal advice and assist in managing various stages of regulatory inquiries and consequent litigation in relation to matters pending before national regulators, as well as...