Clinical Program Manager

Your new role as a Clinical Program Manager involves overseeing and conducting clinical evaluations to support product registrations, market access, and claims. You will be responsible for managing certification and regulatory submission of new products through the clinical evaluation process to ensure compliance.Key Responsibilities:Manage and conduct...

Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved.Please note that this position is office based to be filled at our headquarters office in Covington, KY or the office in Raleigh, NC What...

About the RoleAs a Principal Statistical Programmer at ICON Clinical Research, you will be working with a diverse range of clients to lead Phase II & III studies. Your primary responsibilities will include creating, validating, executing, and generating statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables,...

At Hays Portugal, we are seeking a Clinical Program Director to manage and conduct a program of Clinical Evaluations and related clinical activities.This role is responsible for supporting product registrations, market access, claims, and providing regulatory and commercial support.The ideal candidate will have at least 5 years experience in the management...

Clinical Trial Manager (CTM) jobs in The NetherlandsClinical Trial Manager (CTM) jobs involve overseeing and managing all aspects of clinical trials, from planning and initiation to execution and completion.CTMs are responsible for ensuring that clinical trials are conducted in compliance with regulatory requirements, protocol specifications, and Good...

About the PositionThe Clinical Research Associate at ICON is responsible for ensuring the smooth execution of clinical studies. Key responsibilities include coordinating site initiation and monitoring visits, maintaining accurate study documentation, and submitting regulatory submissions as required. This role requires a strong understanding of ICH GCP...

Social network you want to login/join with:Clinical Supply Chain Manager (home-based), LisbonClient:IQVIALocation:Lisbon, PortugalJob Category:OtherEU work permit required:YesJob Reference:60a1b9c2ded8Job Views:4Posted:16.03.2025Expiry Date:30.04.2025Job Description:Job OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic...

At TN Portugal, we are looking for a skilled Clinical Research Manager to join our team. As a key member of our global clinical operations team, you will be responsible for overseeing the execution of clinical trials in Europe.In this role, you will lead a team of clinical research associates and provide guidance on site selection, initiation, monitoring,...

Social network you want to login/join with:Clinical Supply Chain Manager (home-based), LisbonClient:IQVIALocation:Lisbon, PortugalJob Category:OtherEU work permit required:YesJob Reference:60a1b9c2ded8Job Views:4Posted:16.03.2025Expiry Date:30.04.2025Job Description:Job OverviewThe Clinical Supply Chain Manager is responsible for managing the strategic...

Job DescriptionThe Senior Manager of Child and Adolescent Clinical Operations will be responsible for overseeing the day-to-day operations of our child and adolescent clinical programs.This includes:Managing and providing clinical supervision to a team of counsellorsDeveloping and implementing quality management activitiesEnsuring clinical practice is in...

Company OverviewResourcing Life Science supports various Pharmaceutical & Biotech companies globally with clinical and non-clinical development, peri-approval, and market access solutions.Job DescriptionAs a Global Clinical Start Up Manager in Portugal, you will lead cross-functional project teams for assigned studies in the start up phase. Key...

Company OverviewResourcing Life Science is a leading Contract Research Organization (CRO) supporting pharmaceutical and biotech companies worldwide. We provide comprehensive services, including clinical and non-clinical development, market access, and peri-approval support.Job DescriptionAs a Clinical Start-up Manager, you will lead cross-functional project...

Hays Portugal is seeking a skilled professional to fill the position of Clinical Program Manager. This individual will be responsible for managing and conducting clinical evaluations to support product registrations and market access. The ideal candidate will have a strong background in clinical evaluation and excellent communication skills.About the...

Job OverviewWe are seeking a highly skilled Clinical Case Manager to join our team at PrimeVigilance. As a Clinical Case Manager, you will be responsible for managing and processing individual case safety reports (ICSRs) from various sources, including post-marketing and clinical trials.Your primary responsibilities will include processing ICSRs in...

Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Start up Manager in Portugal.Job Overview Leading cross-functional project teams...

Company OverviewOur client, a renowned Global Contract Research Organization (CRO), is dedicated to supporting pharmaceutical and biotechnology companies worldwide. They offer a comprehensive service solution encompassing clinical and non-clinical development, peri-approval, and market access.Job ResponsibilitiesThe successful candidate will lead...

Regulatory Manager, Clinical Trials Regulatory Management (home-based)Apply locations: Lisbon, Portugal; Barcelona, Spain; Sofia, Bulgaria; Ljubljana – Dunajska, Slovenia; Madrid, SpainTime type: Full timePosted on: Posted 2 Days AgoJob requisition id: R1461041RESPONSIBILITIES- Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial...

TN Portugal is seeking an experienced Security Program Manager to join our team. As a key member of our organization, you will play a critical role in safeguarding our digital assets and ensuring compliance with industry standards and regulations.About the CompanyWe are a leading global provider of advanced analytics, technology solutions, and clinical...

.Regulatory Manager, Clinical Trials Regulatory Management (home-based)Apply locations: Lisbon, Portugal; Barcelona, Spain; Sofia, Bulgaria; Ljubljana – Dunajska, Slovenia; Madrid, SpainTime type: Full timePosted on: Posted 2 Days AgoJob requisition id: R1461041RESPONSIBILITIESActs as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial...

Regulatory Manager, Clinical Trials Regulatory Management (home-based)Apply locations: Lisbon, Portugal; Barcelona, Spain; Sofia, Bulgaria; Ljubljana – Dunajska, Slovenia; Madrid, SpainTime type: Full timePosted on: Posted 2 Days AgoJob requisition id: R1461041RESPONSIBILITIESActs as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial...