Clinical Trial Manager
Icon Clinical Research
Clinical Trial Manager - Phase I oncology ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. What you will be doing Manage the day-to-day operations of assigned trials and responsibilities to ensure completion per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements Leads or supports cross-functional trial teams, including vendors Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders Proactively identify and resolve issues that arise during trial conduct; manage escalation of trial-related issues Participate in or lead the development of core trial documents, trial plans and system set-up; participate in preparation and ensure operational excellence of protocol and implementation of appropriate systems, standards, and processes to ensure quality across investigative sites, vendors, and data Participate in or lead preparation of vendor requirements and project scope and selection of trial vendors; effectively manage interactions and escalations with vendor trial team Participate in or lead feasibility assessment and selection of countries and sites for trial conduct Participate in or facilitates site engagement and communications with investigators and/or staff to support trial milestones and deliverables Oversee the clinical aspects of timely data cleaning, data analysis and the availability of top line results; participate in data reviews and review of statistical analysis plans Participate in or lead set-up and implementation of effective investigator and site monitor training; coordinate operational and therapeutic area training for internal and external trial team members Provide oversight and direction to trial team members for trial deliverables Manage clinical trial budget and associated vendor contracts, including tracking and data in associated systems Ensure quality and completeness of TMF for assigned clinical trials Participates in inspection readiness activities including coordination of clinical trial team deliverables Participate in the evaluation and implementation of patient-focused strategies for assigned trials, as applicable Responsible for the management of budgets, timelines and resources for assigned clinical trial responsibilities Your profile BA/BS degree with at least 3 years clinical trial experience or advanced degree (MS/PhD/PharmD) with at least 2 years clinical trial management experience Must have strong knowledge of ICH/GCP guidelines and regulatory requirements Must have knowledge of protocol and clinical drug development processes, clinical trial design, trial planning and management, and monitoring Requires project management skills and trial leadership ability Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability Fluent in English Experience in Phase I oncology Global experience with primary focus on independent vendor set up and management, oncology cohort management and experience in supporting dose escalation safety meetings. May be asked to Work East coast hours if located further West Moderate (~25%) travel required What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family’s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here #J-18808-Ljbffr ICON
- Clinical Trial Manager - Phase I oncologyICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion...SuggestedFull time
$68.4k - $232.8k
...Internal Job Description Job Overview Associate Project Leads (Local Trial Managers) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Associate Project Lead is a member...SuggestedFull timeContract workPart timeLocal areaImmediate startWorldwide$57 - $71.32 per hour
...Job Description Job Description Job Title: Contract Clinical Study Manager Hybrid Raleigh-Durham (RTP) Job Description The Contract... ...a particular focus on recent experience in leading phase 1 trials, clinical study teams, and vendor management. Responsibilities...SuggestedContract workTemporary workWork at officeMonday to FridayDay shift3 days per week$112k - $222k
...implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright... ...best work every day. Join us! What Clinical Operations Site Management Does At Worldwide Clinical Trial Managers (CTMs) and Clinical...SuggestedRemote jobHourly payWork at officeWorldwide- Clinical Trial Manager - Full Service Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market...SuggestedContract workFlexible hours
- ...Chapel Hill, a global leader in higher education, seeks a Senior Clinical Research Coordinator for the UNC Kidney Center in North... ...two years of clinical research experience as a coordinator, strong communication skills, and the ability to manage #J-18808-Ljbffr...
$95.5k - $159k
Raleigh-Durham, North CarolinaClinical Services - Clinical Study Delivery - Clinical Study Management - Project Management /Full-time, Permanent /RemoteProject Management Manage the planning, execution, progress and completion of assigned clinical research projects.Work...Permanent employmentFull time- ...Clinical Research Coordinator I The Clinical Research Coordinator I conducts and manages clinical trials in accordance with the study protocol, GCP, and Velocity's SOPs. Responsibilities Conduct and manage clinical trials in accordance with the study protocol,...Work at officeFlexible hours
- Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission... ...development, moving into phase 3 clinical trial for one of the biggest breakthroughs in... ...deliver. What is the role? The Clinical Trial Manager (CTM) is responsible for managing various...Interim roleWork at office
- ...hundreds of research locations, mobile clinics, and clinicians across the globe, we bring... ...in all aspects of conducting clinical trials. Coordinate and attend pre-study site visits... ..., and patient compliance. Resolve data management queries and correct source data within...Work at officeLocal areaWorldwide
$55k - $85k
...hundreds of research locations, mobile clinics, and clinicians across the globe, we bring... ...in all aspects of conducting clinical trials. Coordinate and attend pre-study site visits... ..., and patient compliance. Resolve data management queries and correct source data within...Full timeContract workTemporary workFor contractorsFor subcontractorWork at officeLocal areaWorldwideVisa sponsorshipWork visaFlexible hours$55k - $85k
...hundreds of research locations, mobile clinics, and clinicians across the globe, we bring... ...in all aspects of conducting clinical trials. Coordinate and attend pre-study site visits... ..., and patient compliance. Resolve data management queries and correct source data within...Full timeTemporary workWork at officeLocal areaWorldwideVisa sponsorshipWork visaFlexible hours$35 - $42 per hour
...Clinical Research Coordinator (CRC) – Raleigh, NC Location: Raleigh, NC Work Setup... ..., contribute to groundbreaking clinical trials, and ensure the highest standards of patient... ...organizational skills in both data management and regulatory documentation. Key Responsibilities...Hourly payFull timePart timeImmediate startRemote workWorldwide- ...needed to thrive in our organization. About the Role The Senior Clinical Project Manager, Clinical Development is responsible for leading the... ...of domestic and/or global postmarketing required clinical trials. The Sr. CPM serves as the operational leader for assigned...Full timeContract workLive inWork at officeWork from home
- ...and research. Patient care We promote health and provide superb clinical care while maintaining our strong tradition of reaching... ...establish and maintain effective working relationships with coworkers, managers, and clients. Ability to manage competing priorities, including...Full timeLive inWork at officeLocal areaAfternoon shift2 days per weekEarly shift
- ...Velocity Clinical Research is an owned and integrated research site organization, providing... ...patients. We are committed to making clinical trials succeed by generating high quality data... ...of a clinical trial team to conduct and manage clinical trial(s) from start up through...Work at officeFlexible hours
- ...A leading biopharmaceutical solutions organization in Morrisville, NC is seeking a Project Manager to support the management of clinical studies. The role involves coordinating study deliverables, managing vendor relationships, and developing risk mitigation strategies...
- Clinical Research Coordinator II - Wake Research Location: Raleigh, NC. Position is on-site... ...collaboratively with clinical research site management and the Principal Investigator to support the successful execution of clinical trials. The CRC II independently manages day‑to‑...Flexible hours
- ...world leading products for use in infection management in bone and soft tissue. Based in Keele,... ...around the world. Job Summary The Clinical Project Manager is a key part in a product... ...diverse study teams to make sure that trials are conducted and executed effectively....For contractorsMonday to Friday
- ...research. Patient care We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved... ...situations and develop effective solutions. Effective time management skills, with the ability to prioritize tasks, meet deadlines,...Live inWork at office
$95k - $175.7k
Description Clinical Project Manager II - Inflammation/ Phase 2b (Sponsor Dedicated/ Remote; Hybrid Foster City, CA Preferred)Syneos Health is... ...Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.No matter what your role is, you’ll take the...Contract workImmediate startRemote workFlexible hours- ...seeks International Medical Graduates for an entry level role in clinical research. Ideal candidates will have at least 3 years of... ...in learning and growing in the field. Responsibilities include managing studies, recruiting participants, and maintaining study documentation...
- ...our diligence to provide the highest quality of data for our clinical research trials. As Revival Research Institute is growing, we are... ...Clinical Research Coordinators are responsible to coordinate and manage multiple studies. They are also responsible for assisting...Full timeWork at office
$77.08k - $98k
...practitioners and producers, as well as state and federal partners; developing and implementing policies and procedures; supervision and management of laboratory section operations; coordinating all personnel functions; developing new services; and oversight of the quality...Night shift- Bolivia 4311 Old Ocean Highway Bolivia, NC 284226357, USA Bolivia 4311 Old Ocean Highway Bolivia, NC 284226357, USA Shallotte 341 Whiteville Road, NW Shallotte, NC 28470, USA Shallotte 341 Whiteville Road, NW Shallotte, NC 28470, USA Join a team that’s been providing...Flexible hours
- ...our diligence to provide the highest quality of data for our clinical research trials. As Revival Research Institute is growing, we are looking... .... Some responsibilities will include coordinating and managing multiple studies. They are also responsible for assisting the...Work at office
- ...A leading health services provider in North Carolina is seeking a Qualified Professional Assistant to provide clinical administrative support and assist in various office functions. The role involves direct interaction with Qualified Professionals, maintaining documentation...Work at officeMonday to Friday
- ...analytics, and cloud, in combination with a fundamental redesign of the scientific user experience to help our clients better capture, manage, integrate, and analyze complex scientific data. We help improve the discovery and manufacturing of new products, improve quality,...Live inWork at officeLocal area
$124.6k - $255.9k
...reaches the right business leader at the right time to drive client and market conversations. This role provides leadership and management support to the team, driving measurable business impact and innovation in research and distribution among account teams, clients,...- The Director, Clinical Quality Assurance is primarily responsible for establishing and leading... ..., Clinical Quality Assurance, will manage activities and projects based on short-term... ...supervisory experience.Extensive clinical trial experience in biological therapies and in...Temporary workWorldwide
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Trial Manager. Be the first to apply!
- clinical project manager Raleigh, NC
- clinical research coordinator Raleigh, NC
- neuroscience clinical research coordinator Raleigh, NC
- clinical trials manager Raleigh, NC
- global clinical trial manager Raleigh, NC
- clinical research remote Raleigh, NC
- clinical trial associate Raleigh, NC
- clinical research Raleigh, NC
- clinical research manager remote Raleigh, NC
- clinical research nurse Raleigh, NC


