Huidige banen gerelateerd aan Sr. Clinical Research Associate - Amsterdam - Allucent
-
Clinical Research Associate
1 week geleden
Amsterdam, Noord-Holland, Nederland NLF Fortrea Netherlands BV VoltijdJob Title: Clinical Research AssociateWe are seeking a highly skilled Clinical Research Associate to join our team in the Netherlands. As a Clinical Research Associate, you will be responsible for monitoring clinical sites, maintaining study files, and conducting pre-study and initiation visits.Key Responsibilities:Monitor study sites independently according...
-
Clinical Research Associate
3 dagen geleden
Amsterdam, Noord-Holland, Nederland NLF Fortrea Netherlands BV VoltijdJob Title: Clinical Research AssociateWe are seeking a highly skilled Clinical Research Associate to join our team in the Netherlands. As a Clinical Research Associate, you will be responsible for monitoring study sites, conducting pre-study and initiation visits, and ensuring the integrity of the data submitted on Case Report Forms (CRFs) or other data...
-
Clinical Research Associate Senior
3 dagen geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdAbout the RoleWe are seeking a highly skilled and experienced Sr. Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesMonitor and manage clinical study sites to ensure compliance with protocol,...
-
Clinical Research Associate
2 weken geleden
Amsterdam, Noord-Holland, Nederland NLF Fortrea Netherlands BV Voltijd**Job Summary**NLF Fortrea Netherlands BV is seeking a highly skilled Clinical Research Associate to join our team in the Netherlands. As a Clinical Research Associate, you will be responsible for monitoring clinical sites, maintaining study files, conducting pre-study and initiation visits, and liaising with vendors.**Key Responsibilities**Monitor study...
-
Senior Clinical Research Associate
2 weken geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdAbout the RoleWe are seeking a highly skilled and experienced Sr. Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesIndependently monitor and control investigational sites to ensure compliance with...
-
Sr. Clinical Research Associate
3 maanden geleden
Amsterdam, Nederland Allucent VoltijdAt Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will...
-
Clinical Research Associate Lead
2 weken geleden
Amsterdam, Noord-Holland, Nederland Edwards Lifesciences VoltijdJob Summary:We are seeking a highly experienced and skilled Clinical Research Associate Lead to join our team at Edwards Lifesciences. As a key member of our clinical operations team, you will be responsible for overseeing and coordinating clinical studies, ensuring compliance with regulatory requirements, and providing guidance and support to study...
-
Clinical Research Associate II
2 dagen geleden
Amsterdam, Noord-Holland, Nederland Parexel VoltijdAbout the RoleParexel is seeking a Clinical Research Associate II to join our Clinical Operations Team in the Netherlands. As a key member of our team, you will be responsible for conducting qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites.Key ResponsibilitiesLeverage your expertise to conduct...
-
Clinical Research Associate II
6 dagen geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in ensuring the success of our clinical trials by monitoring investigational sites, detecting issues, and providing solutions to ensure compliance with SOPs,...
-
Clinical Research Associate II
3 dagen geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdJob Title: Clinical Research Associate IIWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a Clinical Research Associate II, you will play a critical role in ensuring the success of our clinical trials by monitoring investigational sites, detecting issues, and providing solutions to ensure compliance with SOPs,...
-
Senior Clinical Research Associate
1 week geleden
Amsterdam, Noord-Holland, Nederland Parexel VoltijdAbout the RoleParexel is seeking a Senior Clinical Research Associate to join our Clinical Operations Team in the Netherlands. This role can be office-based in Amsterdam or decentralized in the Netherlands.Key ResponsibilitiesConduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites and...
-
Clinical Research Associate II
3 dagen geleden
Amsterdam, Noord-Holland, Nederland Parexel VoltijdAbout the RoleParexel is seeking a Clinical Research Associate II to join our Clinical Operations Team in the Netherlands. As a key member of our team, you will be responsible for conducting qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites.Key ResponsibilitiesLeverage your expertise to conduct...
-
Clinical Research Associate
2 weken geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdAbout the RoleWe are seeking a highly skilled and experienced Sr. Clinical Research Associate to join our team at Allucent. As a key member of our clinical operations team, you will play a critical role in ensuring the successful execution of clinical trials.Key ResponsibilitiesIndependently monitor and control investigational sites to ensure compliance with...
-
Clinical Research Associate
4 maanden geleden
Amsterdam, Nederland Novartis Voltijd**Summary**: Monitort patiëntgegevens & studiegerelateerde informatie met betrekking tot klinische onderzoekslocaties en deelname aan klinische proeven.. Zorgt ervoor dat de onderzoeker zich houdt aan onderzoeksprotocollen, wettelijke vereisten en goede klinische praktijken en levert input in datavalidatieplan. Biedt tijdige en nauwkeurige monitoring van...
-
Clinical Research Associate Lead
2 weken geleden
Amsterdam, Noord-Holland, Nederland Edwards Lifesciences VoltijdJob SummaryWe are seeking a highly experienced Clinical Research Associate Lead to join our team at Edwards Lifesciences. As a key member of our clinical operations team, you will be responsible for overseeing and coordinating clinical studies, ensuring compliance with regulatory requirements, and providing guidance to study teams.Key Responsibilities:Study...
-
Clinical Research Associate II
2 weken geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdAbout the RoleWe are seeking a highly skilled Clinical Research Associate II to join our team at Allucent. As a key member of our clinical operations team, you will be responsible for monitoring and managing clinical trials to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.Key ResponsibilitiesConduct site visits to...
-
Clinical Research Associate II
2 weken geleden
Amsterdam, Nederland Parexel VoltijdWhen our values align, there's no limit to what we can achieve. 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...
-
Senior Clinical Research Associate
2 maanden geleden
Amsterdam, Nederland Parexel VoltijdWhen our values align, there's no limit to what we can achieve. 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...
-
Clinical Research Associate
2 weken geleden
Amsterdam, Noord-Holland, Nederland Allucent VoltijdAbout the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Allucent. As a Clinical Research Associate, you will play a critical role in ensuring the successful execution of clinical trials. Your primary responsibility will be to monitor and manage clinical study sites, ensuring compliance with Good Clinical Practices (GCP),...
-
Clinical Research Associate Lead
5 dagen geleden
Amsterdam, Noord-Holland, Nederland Edwards Lifesciences VoltijdJob SummaryWe are seeking a highly skilled Clinical Research Associate Lead to join our team at Edwards Lifesciences. As a key member of our clinical operations team, you will be responsible for overseeing clinical studies and providing strategic guidance to principal investigators and study sponsors.Key Responsibilities:Oversee and supervise clinical...
Sr. Clinical Research Associate
4 maanden geleden
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.
We are looking for a Sr. Clinical Research Associate (Sr. CRA) to join our A-team (hybrid*/remote). As a Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical studies are performed according to the trial protocol and in compliance with SOPs, applicable regulations, and the principles of Good Clinical Practice.
In this role your key tasks will include:
Governs highest possible quality standards for trial monitoring activities. Conducts all study tasks in compliance with quality, while preserving efficiency and in alignment to the scope of services and budgeted hours. Monitors activities at clinical study sites to assure adherence to protocol, Monitoring Plan, ICH, GCP, SOPs, and applicable regulations and guidelines: Performs efficient site management in line with study budget. Prepares and submits quality Site Visits Reports and Contact reports. Maintains and updates CTMS in compliance with SOPs and study-specific directives. Acts as Document Owner for collected documents. Conducts co-monitoring as needed. Provides functional assistance to the project team members with administrative, logistical, and practical issues, including the tracking, collection, distribution and filing study documentation (CTMS, TMF). Liaises with project team members and Sponsor to track study progress and milestones. Tracks and supervises collection of ongoing study data for purpose of regular project status reporting within agreed timelines. May review essential documents (GLP) as a 2nd line or Independent Reviewer (IR). May participate in organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project specific CRA training. May perform assessment visits. Represents Allucent in the global medical research community, develop and maintain collaborative relationships with investigational sites and sponsor company personnel. Identifies potential logistical/practical problems and propose solutions / contingency plans, with timeframes for resolution. Acts as the lead contact in case several CRAs involved for a same study in same country. Supervises generation of electronic tracking systems and logs to produce status updates, progress reports and general management of the clinical deliverables when needed. May process and track payments to the Institutional Review Boards (IRB), Ethics Committees (EC), Regulatory Authorities, Investigators and /or vendors including timely notification to finance department, as applicable. May participate in meetings with clients. May support project manager/CTL and project functional leads in the project oversight and management. Supports site staff in preparation for study related site audits and inspections. Where applicable, reports Quality Issues and supports the root cause analysis, writing of and resolution of the Corrective and Preventative Actions.Requirements
To be successful you will possess:
At least five years clinical monitoring experience and/or relevant clinical trial experience. Relevant life science degree / medical / nursing background, or combination of education and experience. Excellent understanding and demonstrated application of Good Clinical Practices and applicable Standard Operating Procedures.. Strong written and verbal communication skills including good command of English and local language. Representative, outgoing and client focused. Ability to work in a fast-paced challenging environment of a growing company. Administrative excellence Proficiency with various computer applications such as Word, Excel, and PowerPoint required. Effective clinical monitoring skills (all kind of visits mastered): Demonstrated understanding of applicable medical/therapeutic area knowledge and medical terminology. In-depth knowledge of clinical trials and the critical elements for success in clinical trials. Excellent understanding of the drug development process. Ability to proactively identify and resolve issues in a timely manner. Effective oral and written and presentation communication skills, with the ability to communicate effectively with medical personnel. Effective organizational and time management skills. Ability to manage multiple projects and strong attention to detail. Ability to establish and maintain effective working relationships with co-workers, managers, investigator site personnel and clients. Ability to meet project requirements. Proven flexibility and adaptability. Ability to work in a team or independently and to effectively prioritize tasks. Ability to perform travel an average of 8 days on site per month, depending on project needs.Benefits
Benefits of working at Allucent include:
Comprehensive benefits package per location Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for remote/hybrid* working depending on location Leadership and mentoring opportunities Participation in our Buddy Program as a new or existing employee Internal growth opportunities and career progression Financially rewarding internal employee referral program Access to online soft-skills and technical training via GoodHabitz and internal platformsDisclaimers:
*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our .
“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
#LI_BL1
