Associate Manager, Clinical Trials Regulatory Management

Prepares and / or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects. RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on global projects which may be complexAbility to administratively and technically / scientifically review core scientific documentation...

Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs RESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customer Ability to...

Overview: CLINICAL RESEARCH ASSOCIATE MADRID - SINGLE SPONSOR TFS HealthScience is excited to be expanding our SRS** **team and we are looking for an experienced, highly motivated regional Senior Clinical Research Associate (CRA) who shares our vision of providing clinical research excellence. Our **SRS** team is a highly experienced international group of...

**Company Description** **Job Description** SMA III** As a Study Management Associate III, you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Study Management Associate III works as an independent, contributing member of a...

We are looking for General Practitioners or Physicians for our clinics around Europe.These profiles will be in charge of clinical trials as principals, and therefore experience in this field is required.Minimum of two years as a Principal during clinical trials.Minimum of two completed clinical trials as Principal.

Precision for Medicine (CRO) are recruiting a Regulatory Manager to join our team, candidates can be based in the following countries: UK, Spain, Hungary, Slovakia, Serbia, Romania or Poland. Position Summary: The Regulatory Manager (RM) provides regulatory strategy and development guidance for optimal conduct of clinical trials, regulatory agency meetings,...

We are looking for General Practitioners or Physicians for our clinics around Europe. These profiles will be in charge of clinical trials as principals, and therefore experience in this field is required. Minimum of two years as a Principal during clinical trials.Minimum of two completed clinical trials as Principal. #J-18808-Ljbffr

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

**Company Description** **Job Description** SMA III** As a Clinical Trial Manager, you will be part of a dynamic, centralized study management team that is responsible for the execution of our global clinical trials and a key member of the study team. The Clinical Trial Manager works as an independent, contributing member of a cross-functional and global...

Clinical Project Manager-230003CJ **Applicants are required to read, write, and speak the following languages***: English, Spanish **Preferred Qualifications** Cerner Enviza (an Oracle company) is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies....

Job DescriptionYou will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors. You willReview external vendor quotationsMaintain vendor databases and tracking systemsSupport vendor identification, assessment...

Job Description You will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors.  You will Review external vendor quotations Maintain vendor databases and tracking systems Support vendor identification,...

Company Description Ergomed PLC is a rapidly expanding full service mid-sized CRO specialising in Oncology and Rare Disease. Since its foundation in 1997 the company has grown organically and steadily by making strategic investments and landmark acquisitions, with operations in Europe, North America and Asia Our company allows for employee visibility (you...

Job Description You will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors.  You will Review external vendor quotations Maintain vendor databases and tracking systems Support vendor...

Job DescriptionYou will be responsible for supporting the establishment of approaches, processes and information flow, along with building strong relationships to ensure effective collaboration between PSI teams and PSI vendors. You willReview external vendor quotationsMaintain vendor databases and tracking systemsSupport vendor identification, assessment...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Job Overview Review & approve investigations, Root Cause Analysis (RCA), Corrective and Preventive Action (CAPA) and Effectiveness Check (EC) plans and track till closure for medium / high-risk / complex quality events arising from Quality Issues, Audits, Inspections or during similar QA activities. Perform Quality Event management within QA-CAPA Center Of...

**Job Title**:Clinical Trial Manager**Job Location**: Madrid, Spain (Home based - any Spain location considered)**Job Overview**: The Clinical Trial Manager is responsible for the day-to-day leadership and management of monitoring services for clinical projects, including direct communication and interaction with investigative sites, Clinical Research...

Associate Study Start-Up Manager IQVIA Biotech Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions: - Oversee the execution of Site Activation...

As Clinical Medical Manager, you will facilitate the execution of Global Clinical Trials related to Cardiovascular, NASH, and Alzheimer’s disease (Novo Nordisk New Therapy Areas) by providing medical/scientific expertise and advice based on interactions with KOLs, independent professional associations and patient advocacy associations as...