Associate Project Manager CTD
Kelsterbach
Vollzeit
Marken
… investigator sites, local and regional depots, HHC providers and clinical trial participants Expanded Access Programs. Providing the client with a primary … for the successful planning, execution, monitoring, control and closure of clinical supply and/or patient centric services projects. Main Duties and … Title: Associate Project Manager CTD Job Purpose: The main purpose of the Project Manager’s …Regional Clinical Trial Associate StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d)
München
Vollzeit
MSD
… Supporting budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals. Responsibilities include, but are not … Our Clinical Research and Pharmacovigilance team push the boundaries of global … operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, …Clinical TrialClinical Program Lead
Biberach an der Riß
Vollzeit
BI International GmbH
… Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, … at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: … you review and approve publications within your project in collaboration associate Head of Medicine. As a Senior Clinical Program Leader, you: You author …Regional Clinical Management Associate Stellenangebote
Regional Clinical Trial Management Associate
Home Office
Vollzeit
BeiGene
… in ensuring compliance including completeness and quality checks of the trial master file (TMF) Demonstrates basic clinical operations knowledge and … this position General Description: Role will support the study team with Clinical Operations tasks, and/or assist in ensuring compliance including … and/or review of Clinical Operations Work Instructions and SOPs The Junior Associate role in Clinical Operations is an entry level position This job …Management AssociateAssociate Director, Field Medical Advisor, Northern Germany
Home Office
Vollzeit
Moderna
… narratives across Moderna’s therapeutic areas, including clinical trial data and research findings, to support the medical and scientific … scientific narratives across Moderna’s therapeutic areas, including clinical trial data and research findings, to support the medical and scientific … scientific societies, public health institutions at the national and / or regional level, advisory and professional bodies, patient advocacy groups and …Regional Associate StellenangeboteClinical Site Monitor I/ II - FSP/ Germany/Homebased
Home Office
Vollzeit
Parexel
… trials experience. Experience in utilizing systems like Siebel Clinical trial Management System (CTMS), electronic trial Master File (eTMF), electronic … Parexel FSP is hiring for a home-based Clinical Site Monitor I or II. Single sponsor dedicated to a worldwide … Experience required: A minimum of 1 year experience as a Clinical Research Associate with demonstrated experience in monitoring (virtual or onsite). Oncology …Clinical Trial Associate StellenangeboteClinical Research Associate (Germany)
München
Vollzeit
Precision for Medicine
… therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and … therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and … would be an advantage For Senior CRAs, understanding of financial management and mentoring experience would be desirable We invite you to learn more …Regional Clinical Management Associate
Contracts Associate
Deutschland
Vollzeit
ICON
… organisation with specific experience negotiating clinical trial agreements with sites Exemplary communication skills including a fluency … as a Contracts Associate you will negotiate contracts and budgets with clinical sites across Germany. We are searching for a professional who has already … Working as a Contracts Associate you will negotiate contracts and budgets with clinical sites across …Clinical Trial ManagementClinical Associate
Frankfurt am Main
Vollzeit
Icon plc
… ensure study files are always inspection ready. Assist project teams with trial progress tracking by updating the Clinical trial Management systems, … About the role ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical … succeed and a passion that ensures what we do, we do well. Senior Clinical Associate - office base What will you be doing? Maintains study documents and …Trial Associate StellenangeboteAssociate Director* Bioanalytics
Mainz
Vollzeit
BioNTech AG
… biomarker testing and biopotency assay strategy of multiple clinical trial projects Selection of appropriate analytical technologies in collaboration … methods for PK, ADA and biomarker analytics required for all phases of clinical trials as well as cell based biopotency methods, each outsourced to … to be a part of creating hope for a healthy future in many people's lives. Associate Director* Bioanalytics As subject matter expert (SME) Bioanalytics you are …Trial ManagementAssociate Director* Operational Quality Assurance - individualized mRNA cancer vaccine materials
Mainz
Vollzeit
BioNTech AG
… Product Lifecycle Management of BNT individualized mRNA clinical trial projects. As part of our Operational QA Team, you will be based in Mainz … phase-appropriate Product Lifecycle Management of BNT individualized mRNA clinical trial projects. As part of our Operational QA Team, you will be based in … to be a part of creating hope for a healthy future in many people's lives. Associate Director* Operational Quality Assurance - individualized mRNA cancer …Regional Clinical TrialClinical Research Associate (all levels), Oncology, FSP, home based, client dedicated
Home Office
Vollzeit
Syneos - Clinical and Corporate - Prod
… and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in … Description Clinical Research Associate - home based, sponsor dedicated, flexible level based … Description Clinical Research Associate - home based, sponsor dedicated, flexible level based on your work …Regional Clinical Management
Study Start Up Associate I
Home Office
Vollzeit
ICON
… sure that physicians at our research sites are prepared to start the trial of investigational, new pharmaceutical and biological products for … ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment … will be doing: Initiate and coordinate activities and essential documents management during start-up towards the compilation of a high-quality Investigator …Regional Trial Management StellenangeboteClinical Site Manager
Deutschland
Vollzeit
ICON
… activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of the … execute Site Engagement Strategy/Plan working closely with the Sponsors Clinical Team and key internal stake holders throughout the life cycle Engages with … clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies) BS or MSc. degree in a life …Trial Associate Stellenangebote