Associate Clinical Project Manager

hace 2 meses


Madrid, España Ora A tiempo completo

.POSITION TITLE: Associate Clinical Project ManagerDEPARTMENT: Ora EuropeLOCATION: Remote, UK, Spain, Italy or PolandOra Values the Daily Practice of ...Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor----------------------------------------At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past 45 years, our expert teams have helped earn more than 85 new product approvals. Ora's pre-clinical and clinical models, unique methodologies, integrated clinical data solutions, and global regulatory strategies have been refined and proven across thousands of global projects. Today, our team continues to expand across the globe, with over 600 employees across North America, Europe, Asia, and Latin America.The Role:Ora's Associate Clinical Project Managers (Associate CPM) are critical in driving clinical ophthalmic projects forward utilizing best practices in order to ensure budgets, timelines, and clinical trial requirements are being met on behalf of the sponsor. This role will work independently and with oversight as needed to manage cross functional project teams. Associate CPM's have active involvement in each assigned project in order to meet milestones, resolve issues and/ or conflicts in addition to frequent interactions with the study team including but not limited to clinical trial associates, monitoring, clinical research coordinators, investigators and senior management. They are responsible for creating project plans, with direction, and provide weekly budget and progress reviews for each study in addition to preparing high-quality reports.What You'll Do:Independently and with oversight as needed manages cross functional project teams derived from the groups within clinical development to deliver a high-quality clinical trial(s) in compliance with all regulations and SOPs.Works with functional areas on initiating, planning, executing, controlling, closing and resourcing clinical trial projects. The Associate CPM acts as an operational nexus or focal point for interdepartmental and intradepartmental groups (e.G. stats, data management, safety, manufacturing, regulatory, vendors), coordinating these different groups in a matrix environment to drive and complete clinical programs.Independently and with oversight as needed, reviews protocol, source documents and CRFs and tracks them to completion.With oversight, responsible for creating and maintaining project timelines for each project and uses these timelines to track and manage a project's progress.Responsible for creating Project Plans, with direction from senior leadership Roles and Responsibility Tables and Communication Plans) and weekly project budget and progress reviews for each study



  • Madrid, España Ares Consultores A tiempo completo

    .POSITION TITLE: Associate Clinical Project Manager DEPARTMENT: Ora Europe LOCATION: Remote, UK, Spain, Italy or Poland Ora Values the Daily Practice of ... Prioritizing Kindness, Operational Excellence, Cultivating Joy, Scientific Rigor.At Ora, we are building the future of ophthalmic clinical research.As the world's leading full-service ophthalmic drug and...


  • Madrid, España Ora A tiempo completo

    **POSITION TITLE**:Associate Clinical Project Manager **DEPARTMENT**: Ora Europe **LOCATION**: Remote, UK, Spain, Italy or Poland **_ Ora Values the Daily Practice of_** - Prioritizing Kindness - Operational Excellence - Cultivating Joy - Scientific Rigor_ - _______________________________________ At Ora, we are building the future of ophthalmic clinical...


  • Madrid, España Ares Consultores A tiempo completo

    .POSITION TITLE: Associate Clinical Project ManagerDEPARTMENT: Ora EuropeLOCATION: Remote, UK, Spain, Italy or PolandOra Values the Daily Practice of ... Prioritizing Kindness, Operational Excellence, Cultivating Joy, Scientific Rigor.At Ora, we are building the future of ophthalmic clinical research.As the world's leading full-service ophthalmic drug and...


  • Madrid, España EastHORN Clinical Services A tiempo completo

    **Job summary**: As a **Clinical Project Administrator, **you will be expected to provide clerical support to project team and assist in project management activities working with Project Managers. You will be involved in key activities, such as collecting and submitting documents to Regulatory Authorities and Ethics Committees. Additionally, you will be...


  • Madrid, España buscojobs España A tiempo completo

    Associate Clinical Project Manager - (A295) Madrid EUR 50.000 - 70.000 POSITION TITLE: Associate Clinical Project Manager DEPARTMENT: Ora Europe LOCATION: Remote, UK, Spain, Italy or Poland Ora Values the Daily Practice of ... Prioritizing Kindness, Operational Excellence, Cultivating Joy, Scientific Rigor. At Ora, we are building the future of ophthalmic...


  • Madrid, España Ares Consultores A tiempo completo

    .Job Title : Associate Clinical Trial Regulatory Manager (ROW)Job Location : Madrid, Spain (Home-based, any location in Spain considered)Job Overview : The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure.The Associate Clinical Trial Regulatory...


  • Madrid, España Ares Consultores A tiempo completo

    POSITION TITLE: Associate Clinical Project ManagerDEPARTMENT: Ora EuropeLOCATION: Remote, UK, Spain, Italy or PolandOra Values the Daily Practice of ... Prioritizing Kindness, Operational Excellence, Cultivating Joy, Scientific Rigor.At Ora, we are building the future of ophthalmic clinical research.As the world's leading full-service ophthalmic drug and...


  • Madrid, España Ares Consultores A tiempo completo

    .Job Title : Associate Clinical Trial Regulatory Manager (ROW) Job Location : Madrid, Spain (Home-based, any location in Spain considered) Job Overview : The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure.The Associate Clinical Trial Regulatory...


  • Madrid, España EastHORN Clinical Services A tiempo completo

    **Job summary**: As an Clinical Research Associate you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties. You...


  • Madrid, España EastHORN Clinical Services A tiempo completo

    As an experienced **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties. You...


  • Madrid, España Clinipace A tiempo completo

    **Job Title**:Associate Clinical Trial Regulatory Manager (ROW) **Job Location**: Madrid, Spain (Home-based, any location in Spain considered) **Job Overview**: The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure. The Associate Clinical Trial...


  • Madrid, España TFS HealthScience A tiempo completo

    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...


  • Madrid, España EastHORN Clinical Services A tiempo completo

    **Job summary**: As an experienced **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and...


  • Madrid, España Ares Consultores A tiempo completo

    Job Title: Associate Clinical Trial Regulatory Manager (ROW)Job Location: Madrid, Spain (Home-based, any location in Spain considered)Job Overview: The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure.The Associate Clinical Trial Regulatory...


  • Madrid, España ClinChoice A tiempo completo

    ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Senior Clinical Project Manager to join their internal team in Spain. You will work on projects from our varied...


  • Madrid, España ARES CONSULTORES A tiempo completo

    Job Title : Associate Clinical Trial Regulatory Manager (ROW) Job Location : Madrid, Spain (Home-based, any location in Spain considered) Job Overview : The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure. The Associate Clinical Trial Regulatory...


  • Madrid, España buscojobs España A tiempo completo

    Job Title : Associate Clinical Trial Regulatory Manager (ROW) Job Location : Madrid, Spain (Home-based, any location in Spain considered) Job Overview : The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure. The Associate Clinical Trial...


  • Madrid, España Ares Consultores A tiempo completo

    Job Title : Associate Clinical Trial Regulatory Manager (ROW) Job Location : Madrid, Spain (Home-based, any location in Spain considered) Job Overview : The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure.The Associate Clinical Trial Regulatory...


  • Madrid, España TFS HealthScience A tiempo completo

    Overview: **Clinical Research Associate Madrid** 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 professionals...


  • Madrid, España Oxford Global Resources A tiempo completo

    **Clinical Project Manager**: - Location: Madrid, Spain - Contact: Susagna Sastre Magem - Job type: Permanent - Contact phone: +34 935 222 338 - Industry: Pharmaceutical, Life Sciences, Biotechnology, Clinical Research Oxford Global Resources is looking for a Clinical Project Manager who will join a non-profit Scientific Association, leader in clinical and...