Clinical Trial Manager
ICON
Local Trial Manager - Early Development Multi Therapeutic 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. The LTM for early development multi TA will manage and oversee the following throughout the study: Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable. Execution of local milestones from feasibility through study close out. Resourcing of country-level roles, including support with transitions, in collaboration and agreement with the study Functional Manager (FM). Inspection Readiness and AQR at the country level. Close collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary. Efficient communication with the Clinical Trial Managers (CTMs), Clinical Operations and the Global Trial Leader (GTL) to oversee trial excellence. Country level ad hoc meetings during any phase of the study that are needed to address unexpected circumstances that might impact country or study level deliverables. Close partnership with the study FM to provide updates, discuss hurdles, timelines/resources, and potential risks, and assist with documentation, such as storyboards, lessons-learned, metrics, etc., that may be required by leadership. Autonomy with execution of local trial management services Depth of knowledge with local trial management services Process leadership What you need to have BA/BS degree. Degree in a health or science related field. 2+ years of trial end to end management experience Start-up & Database Locks/Cleaning experience preferred Early Development multi therapeutic experience required Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home according to business needs. Proficient in speaking and writing the country language and English. Good written and oral communication skills as appropriate To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status 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 Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles. Are you a current ICON Employee? Please click here to apply #J-18808-Ljbffr
$130k - $160k
...Position: Senior Clinical Trial Manager Department: Development Location: Remote with up to 25% travel Reports To: Director of Clinical Operations Position Summary The Senior Clinical Trial Manager will be responsible for the management of one or more clinical trials...SuggestedRemote workWork from home$140k - $170k
...Biotechnology Inc. does not accept unsolicited resumes or candidates from outside staffing agencies or recruiters. The Senior Clinical Trial Manager (Senior CTM) is responsible for the successful execution of clinical trials from the protocol concept through the clinical...SuggestedFull timeContract workWork at officeRemote workWork from homeHome officeMonday to FridayWeekend workAfternoon shift$116.71k - $145.88k
...A leading healthcare company is seeking a Project Manager for Clinical Research to oversee the design and conduct of clinical trials in a remote setup. The successful candidate will ensure compliance with ethical standards, support study documentation, and lead a team...SuggestedRemote work$140k - $170k
Puma Biotechnology, Inc. is seeking a Senior Clinical Trial Manager in Los Angeles, California. This role involves overseeing all clinical aspects of trials, ensuring compliance with GCP guidelines, and managing study timelines. The ideal candidate will have at least 6...SuggestedRemote jobFull time$36.37 - $58.52 per hour
...The Department of Psychiatry is seeking to hire a Clinical Research Coordinator to join the TMS Research Service. You will contribute to the overall operational management of clinical research activities from design, set up, conduct, through closeout. Primary duties include...SuggestedWork at office$71k - $80k
...Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its... ...'s Disease prevention and treatment drug trials, and our doctors were the largest contributors... ...produced quality work. Job Duties Manage daily operations for assigned clinical...Full time$29 - $33 per hour
...of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well... ...quality people, teamwork, and highly experienced clinical research managers with a history of success. Along with an exceptional work...Hourly payFull timeWork at officeMonday to FridayShift workNight shift- ...Clinical Research Coordinator (Oncology) We are seeking an experienced Clinical Research Coordinator... ...role in ensuring continuity of clinical trials and patient care during a pivotal period.... .... Key Responsibilities: Coordinate and manage oncology clinical trials in compliance...Immediate startRemote workRelocation
$22 - $26 per hour
...Clinical Research Coordinator Pasadena, CA 91107 Overview Salary Range $22.00 -... ...principal investigators in recruiting and management research studies directly affecting the... ...aspects of patients involved in clinical trials. Ensure procedures are completed...Hourly payWork at officeLocal area$35 - $40 per hour
...Clinical Research Coordinator – Los Angeles, CA (90033) Position Overview: This role is with... ...team and lead the execution of clinical trials. This new site-based role requires someone... ...integrity. Our ideal candidate will manage a significant portion of the studies, ensuring...Monday to Friday$45k - $100k
...Clinical Research Coordinator I/II/III Opportunities – Multiple Locations Nationwide At Headlands... ..., we are dedicated to enhancing clinical trial delivery within our communities. As a... ...study visits, collecting and managing data, and ensuring studies are conducted...Internship- ...Clinical Research Coordinator The Clinical Research Coordinator (CRC) supports the conduct of clinical trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory guidelines. This role involves direct interaction...H1bMonday to Friday
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator I to coordinate clinical studies, manage patient data, and ensure compliance with regulatory guidelines. The role requires a High School Diploma, with a preference for a bachelor's degree in a related...
- Cedars-Sinai is looking for a Clinical Research Coordinator I in Los Angeles to oversee clinical studies, ensuring compliance with federal regulations while coordinating with patients and medical personnel. The ideal candidate should hold at least a High School Diploma...
$24 - $39.76 per hour
A leading medical center in Los Angeles seeks a Clinical Research Coordinator I to manage patient scheduling, document research activities, and comply with federal regulations. Ideal candidates have a high school diploma or GED, with a preference for a bachelor's degree...Hourly payFull time- Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator to support clinical research protocols effectively. This role involves processing laboratory specimens, maintaining records, and facilitating patient recruitment. The ideal candidate holds a High School...Remote work
- A leading medical center in Los Angeles is seeking a Clinical Research Coordinator II to manage study coordination, including patient scheduling and data collection. The role requires effective communication with medical personnel and compliance with FDA regulations. Candidates...
- Direct Jobs is seeking a Clinical Research Coordinator I in Los Angeles, CA. The role involves independently managing clinical research studies, ensuring compliance with federal regulations, and maintaining patient confidentiality. Responsibilities include coordinating...
- The University of California - Los Angeles Health is seeking a Clinical Research Coordinator to manage clinical research studies from design to closeout. This role requires strong communication and organizational skills, along with the ability to comply with regulations...
- Cedars-Sinai is seeking a Clinical Research Coordinator I who will be responsible for coordinating clinical research studies and ensuring compliance with federal and local regulations. The role requires scheduling participants, documenting conditions, and maintaining patient...Local area
$38 - $40 per hour
Clinical Research Coordinator - Spanish Bilingual Compensation: ~ ($38-$40/hr) Project We are seeking a high-level Spanish speaking... ...study lifecycle—from site activation and patient enrollment to IP management and data close-out. Strict Requirements Clinical Skills:...Private practiceLocal areaRemote workRelocation$25 - $40 per hour
Part-time employment to start. This position is to fulfill a role for Clinical Research Coordinator at multiple sites (Oxnard, Palmdale, Valencia, Sherman Oaks, West Hills, Downtown LA, Inglewood). Some days you will work remote. Past experience as a Clinical Research...Hourly payPart timeLive inRemote work- Overview EXPERIENCED Clinical Research Coordinator - Onsite Job Details: 15-20 hours/week for the first 3 months... ...Coordinator (CRC) to join our dynamic clinical trials team. The CRC will plan, coordinate, and manage all activities associated with the initiation, conduct...Full timeWork at officeLocal areaRemote workVisa sponsorship
- ...Clinical Research Coordinator I Join us for an exciting opportunity with one of the most outstanding and dynamic places known nationally... ...patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent...Work at officeLocal area
- RDI is a trial management organization connecting IVD manufacturers and pharmaceutical companies with a network of doctors participating in... ...provide sample procurement, conduct testing, and simplify the clinical trial process for our clients while recruiting, educating,...
- A leading healthcare institution in Los Angeles seeks a Clinical Research Coordinator II to independently manage clinical trials. The role involves screening potential patients, maintaining strict compliance with FDA and IRB guidelines, data documentation, and presenting...
$36.37 - $58.52 per hour
...UCLA Health is seeking an experienced Clinical Research Coordinator in Los Angeles, California, to support interventional clinical trials. The role involves managing study activities, including participant recruitment, study implementation, data collection, and ensuring...Hourly pay$29.28 - $47.1 per hour
...Direct Jobs is seeking an Assistant Clinical Research Coordinator in Los Angeles, CA, to support the management of clinical research and trial activities. The ideal candidate will have a Bachelor's degree and at least 2 years of experience in study coordination. Roles...Hourly payFlexible hours- ...A clinical research organization in Pasadena is seeking a Clinical Research Coordinator to manage trial activities while ensuring compliance with regulations and protocols. The ideal candidate will possess a relevant degree and experience in clinical assessments, exhibiting...
$36.37 - $58.52 per hour
...UCLA Health's Department of Psychiatry is hiring a Clinical Research Coordinator to support their TMS Research Service. This role involves managing clinical research activities, ensuring compliance with various regulations, and coordinating all study-related tasks from...
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