At PPD, you will make a positive difference for others, help to improve the quality of lives and make the world a healthier place. Supports scheduling of client and/or internal meetings with completion of related meeting minutes. Clinical Trial Coordinator - PPD, part of Thermo Fisher Scientific We are vital links between an idea for a new medicine and the people who need it. Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems Ability to successfully complete PPD clinical training program Self-motivated, positive attitude and good interpersonal skills Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members. - Worked with catering staff to make hot beverages, deliver and adapt meals for patients with various dietary requirements, improving my hospitality and problem-solving skills. Your dedicated line manager, mentors, work buddies and experienced team members and managers will encourage and inspire you. Company will work u like a dog; they are not flexible and you WILL stay in fear of loosing job if ur sick and need to be gone. Given our scope and the complexity of our clients trials, you will have many opportunities to move and grow across our organization. Youll learn soft skills, attend instructor-led live sessions and receive role-play and field training to ensure the confidence, critical-thinking and relationship-building skills essential to success. Provide site selection support for awarded projects and be responsible for pulling regulatory country submissions together in order to activate investigative sites. This number represents the median, which is the midpoint of the ranges from our proprietary Total Pay Estimate model and based on salaries collected from our users. Trial Free interview details posted anonymously by PPD interview candidates. We encourage you to hear what Daniel Jones, vice president of clinical operations, North America Regional Head has to say about the importance of being a CRA at PPD. Submit Close. The clinical monitoring team works with many groups within PPD to ensure the oversight of data quality and integrity. The estimated total pay for a Clinical Trial Coordinator at PPD is $46 per hour. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health! events listings. Whether youre working remotely, at clinical sites or in-house, PPDs management teams nurture your internal connections. Our continuous training program for clinical researchers, CRA Drive, provides access to development resources for further progression into on-site or remote CRA roles. RN, PharmD, M.D.) Leverage your professional network, and get hired. As a Clinical Trial Coordinator, you will provide technical and administrative support to your assigned clinical project team.You work with a high attention to detail, reviewing documentation, coordinating project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. Source: www.glassdoor.com The estimated base pay is $32 per hour. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document. Please be aware that if you continue browsing the website without changing your cookie settings, you consent to this. Whether you participate as an existing employee or a new, external hire, youll find the extensive training and development resources and support essential to realizing your most important goals throughout each phase of your CRA career. (This will open in a new window from which you will be automatically redirected to an external site after 5 seconds). 2K followers 500+ connections. Work exclusively for one of our strategic pharmaceutical partners to collaborate with the clients teams, systems and processes on behalf of PPD. After graduating, I was more grounded in the knowledge and application of clinical research tenets, could identify my strengths and felt empowered to reach out to my trainers and peers., They truly care about my career goals and where I want to be, and they motivate me to meet those goals., I was promoted to CTM in October 2019, with the same client who accepted me as a brand-new CRA. Proactively communicates any risks to project leads and line manager as appropriate. Something went wrong. PPD PPD, a leader in introducing risk-based monitoring into all studies, uses data analytics to continually assess processes throughout our sites. - Brought a positive attitude when talking with patients and their families. We are vital links between an idea for a new medicine and the people who need it. Based on 7 salaries posted anonymously by PPD Clinical Trial Coordinator employees in Bromley. AWARD-WINNING TRAINING AND ADVANCEMENT Its the most important step in confirming whether a new drug or treatment is safe and effective in people. PPD is a leading globalcontract research organizationproviding comprehensive, integrateddrug development,laboratoryand lifecycle management services. We are the people of PPD clinical research services . For CRAs, we offer regular promotion cycles throughout the year, providing you the opportunity to grow your career at your own pace and maximize your potential. between a patient/site visitor and his/her physician. We are the people of PPD thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. We are the people of PPD - thousands of employees in locations world . We invite you to listen to global clinical development David Johnston,senior vice president and presidentoftheClinicalResearchbusiness of Thermo Fisher Scientific, Emma Sealey, senior clinical team manager based in Australia, Amber Lee, senior vice president of clinical operations, and several graduates of the CRA Academy around the world. As a Clinical Trial Coordinator (Client-dedicated), you will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable, working on client studies only, using their clinical systems and SOPs. The team I love the CRA role., What a huge contribution to PPD, bringing all these talented people into our workforce, while offering them great growth opportunities., -Jan-Maarten, current Senior Director of Project Management. Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools; Reviews regulatory documents for proper . You can also work in a client-dedicated capacity or support client projects in both on-site and remote roles. If youre enthusiastic and committed to success, here are three roles to consider at PPD. PPD is dedicated to supporting and fostering work-life balance and flexibility. You can unsubscribe from these emails at any time. Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites. Our clinical monitoring team ensures the highest quality review of data and effective interaction with sites via both remote and on-site monitoring throughout a study. Training magazine has recognized PPD for innovative training practices for 10 consecutive years. PES University. Performance metrics for Academy CRAs are reviewed regularly to closely monitor quality standards. Ensures allocated tasks are performed on time, within budget and to a high-quality standard. . As a PPD Clinical Trial Coordinator you will provide administrative and technical support to the Project Team. For more information on our use of cookies, please review our cookie policy. According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. It has been an incredible opportunity, and I have learned a lot. ; Job suggestion you might be interested based on your profile. Every medical advance starts with a clinical trial. We are the people of PPD clinical research This fully salaried position features comprehensive training and development opportunities, so you can explore your potential as you build a career. In all instances, you will be customer-focused and represent PPD, in addition to receiving our support and management. Evidence Synthesis, Modeling and Communication, PPD Functional Service Partnership Solutions, Bioanalytical Lab Experience and Expertise, Advantages of Being a Clinical Trial Investigator, Clinical Trial Investigators Database Registration. We offer continued career advancement opportunities, award winning training and benefits focused on the health . Visit the Career Advice Hub to see tips on interviewing and resume writing. Our CRAs work closely with our sites and study teams to ensure quality study data, and that the quality of our work can withstand scrutiny. Or you might be placed on an FSP project, to which youll contribute to meeting the clients needs and to the wider FSP group. According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. Click here to see the total pay, recent salaries shared and more! Report this profile . Clinical Trial Coordinator, Different locations in Poland job in Warsaw, Poland with PPD. For more information on our use of cookies, please review our cookie policy. Cambridge University Hospitals NHS Foundation Trust. We are currently seeking a Clinical Trial Coordinator to join our team in Switzerland, who will provide administrative and technical support to the Project Teams. Supports audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document. As a Clinical Research Coordinator, you will be a key member impacting the development and research for therapeutics for patients. Ability to work in a team or independently as required, Solid organizational skills and strong attention to detail, with demonstrated ability to handle multiple tasks efficiently and effectively, Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency, Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines, Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout, Strong English language and grammar skills and proficient local language skills as needed, Strong computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems, Ability to successfully complete PPD clinical training program, Self-motivated, positive attitude and solid interpersonal skills. 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