Clinical Document Coordinator

About the PositionAs a Clinical Drug Supply Manager, you will play a crucial role in ensuring the successful management of clinical trials by coordinating drug supply and packaging, labeling, and distribution of clinical trial supplies.This position requires excellent communication and project management skills, as well as the ability to work independently...

We are seeking a highly organized and detail-focused Design Documentation Coordinator to join our product development team at Knoll Inc. As a key member of our team, you will be responsible for creating, maintaining and updating product documentation, including 2D drawings, technical specifications, and user manuals.Your primary duties will include:Creating...

As a Clinical Drug Supply Manager at Genmab, you will play a critical role in ensuring the success of our clinical trials. You will be responsible for managing the outsourcing of packaging, labeling, and distribution of clinical trial supplies for early- and late-stage trials. The successful candidate will work closely with GMP QA and our CMOs to ensure...

About UsWe are Novartis, a leading global healthcare company.Job DescriptionThe Medical Lead will be responsible for ensuring medical enquiries are responded to in a high quality and timely manner. This includes establishing standard response documents for frequently asked questions.This role involves providing medical/scientific input into the development...

Role OverviewAs a Sr. Associate/Manager in the CTD&T team, you will play a crucial role in ensuring successful clinical trial conduct and reporting.Your key responsibilities include managing, tracking, and overseeing public disclosure of clinical trial protocols, results, and document redaction.Additionally, you will develop and maintain timelines for...

About UsGenmab is an international biotechnology company dedicated to improving lives through innovative antibody therapeutics. Our core purpose drives us to strive towards excellence in our field, and we believe that being unique, determined, and authentic is essential to fulfilling our mission.Job DescriptionThis Sr. Associate/Manager position in our...

SRG Copenhagen, Capital Region of Denmark, DenmarkClinic DirectorPermanentUp to 984,000 DKK (depending on skills, experience and background)Scope of the role:This is a rewarding, patient-centric role in which you will have responsibility for a range of services and teams in the organisation, utilising your background in the fields of...

TruLab, a pioneering technology company in RTP-based mobile solutions, empowers drug developers to track biosamples in real-time and ensure protocol compliance in clinical studies.Job Summary:We seek an experienced Project Manager for our EU operations to oversee the success of our biotech/pharma clients and end-users at clinical testing sites. As a key...

We are seeking a highly motivated Project Manager to join our team in Copenhagen, Denmark. As a key member of our EU operations, you will be responsible for overseeing the success of our biotech/pharma clients and end-users at clinical testing sites.Responsibilities:Cultivate and maintain relationships with our European clients and users.Lead customer calls...

Overview:TFS HealthScience is a pioneering Contract Research Organization (CRO) that empowers biotechnology and pharmaceutical companies to achieve their clinical development goals. With a unique blend of full-service capabilities and global reach, we offer an agile and flexible approach that sets us apart from larger CROs.Key Responsibilities:This Clinical...

**Job Summary**We are looking for a highly motivated and detail-oriented individual to join our team as a Real-Time Operations Coordinator. As a key member of our operations team, you will be responsible for coordinating activities and interactions among diverse groups, both internally and externally, across multiple simultaneous projects.Your primary focus...

About the PositionThis is an entry-level position that offers opportunities for career advancement and personal development as the company expands. As a Customer Success Project Manager, you will serve as the primary liaison between our biotech/pharma clients and end-users at clinical testing sites and laboratories globally.You will cultivate and maintain...

Company OverviewAbout LEO PharmaWe are an ambitious team driven by a high level of integrity, science, and passion for our work. Our Medical Communication team in Global Clinical Development is responsible for planning, managing, and writing clear, concise, and audience-friendly regulatory, scientific, and medical documents.In this role, you will play a...

At Novo Nordisk A/S, we are seeking an experienced Clinical Operations Director to join our team. As a key member of our clinical operations department, you will be responsible for leading the execution of clinical projects in assigned therapeutic areas across Region Europe & Canada (EUCAN). Your primary focus will be on ensuring the timely and successful...

Job DescriptionWe are looking for a Senior Clinical Operations Manager to join our team in Copenhagen, Denmark. The role will involve leading from a strategic point of view the execution of clinical projects in assigned therapeutic areas in all countries of Region Europe & Canada (EUCAN).Your key responsibilities will include following up on the status of...

About the Role We are seeking an experienced Clinical Drug Supply Manager to join our team in Copenhagen, DK or Princeton, NJ. As a Clinical Drug Supply Manager, you will play a critical role in managing outsourcing of packaging, labeling, and distribution of clinical trial supplies for early as well as late-stage Genmab clinical trials. Main...

About the RoleWe are seeking a highly skilled and experienced Senior Clinical Operations Manager to lead our clinical projects in Region Europe & Canada. As a key member of our team, you will be responsible for overseeing the execution of strategic plans with countries in the region, involving stakeholders and ensuring implementation.Key responsibilities...

Job DescriptionKey ResponsibilitiesPlan, Handle, Manage, Structure, and Write Clear Regulatory Documents: As a Medical Writing and Clinical Disclosure Professional, your objective will be to plan, handle, manage, structure, and write clear, concise, and audience-friendly regulatory, scientific, and medical documents fit for purpose.Lead Cross-Functional...

Job SummaryWe are seeking a highly organized and detail-oriented Technical Documentation Manager to join our Fleet Management & Technology team.As a Technical Documentation Manager, you will be responsible for managing vessel technical documentation, assisting project managers, and contributing to the continuous improvement of project management practices.

Clinical Trial Manager, Clinical OperationsRequisition ID: 5984Location: Copenhagen, Danish Capital Region, DKClinical Trial Manager, Clinical OperationsDo you want to join a motivated, focused global development team, work within our strong portfolio, and make a difference to patients living with brain disease? Are you motivated by having the opportunity to...