Clinical Research Coordinator
ICON
Clinical Research Coordinator- McComb, MS 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. As a Clinical Research Coordinator at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do: Your role will involve delivering clinical coordination work to a high standard, working closely with your team and stakeholders. Key responsibilities include: Facilitating the coordination and execution of clinical research studies, including participant recruitment, enrollment, and follow-up activities. Collaborating with principal investigators, study sponsors, and regulatory authorities to ensure compliance with study protocols, regulatory requirements, and ethical standards. Collecting and maintaining accurate and complete clinical trial data, including documentation of adverse events, protocol deviations, and study outcomes. Managing study-related documentation, including informed consent forms, case report forms, and regulatory submissions. Providing support and guidance to study participants, including education, counseling, and assistance with study-related procedures. Your Profile: You will bring relevant clinical coordination experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a relevant scientific discipline or healthcare-related field. Previous experience working in clinical research or healthcare settings preferred. Knowledge of clinical research regulations, including FDA/EMA regulations, ICH-GCP guidelines, and HIPAA requirements. Strong organizational, communication, and interpersonal skills, with the ability to work effectively in a team environment. Detail-oriented with the ability to manage multiple tasks and priorities simultaneously. 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. 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 Research Coordinator- McComb, MSICON 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...Suggested
$25 - $36 per hour
About Us Flourish Research is where clinical trials thrive.Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and...SuggestedHourly payWork at officeMonday to FridayShift work- Flourish Research in Plymouth Meeting, PA is seeking a dedicated clinical research professional to perform protocol-specified patient visits, phlebotomy, and data entry, within an oncology-focused team. The role requires at least two years in clinical research, familiarity...SuggestedHourly pay
- Main Line Health's Clinical Research Center at the Lankenau Institute for Medical Research is seeking a Clinical Research Coordinator II. You will oversee multiple phase II-IV clinical trials, working under investigators and senior staff to ensure quality data collection...Suggested
- ...ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment... ...budget by providing input to study level documents and leading/coordinating local team activities in compliance with SOPs, other...SuggestedLocal areaRemote workWork from homeWork visaFlexible hours
- ...Senior Clinical Project Manager - Remote, US ICON 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...Remote work
- ...Clinical Trial Coordinator Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database...Full timeShift work
$24 per hour
...Clinical CoordinatorNorristown, PAFull-Time$24/hourDailyPay AvailableLooking for More Than Just a Job?At Resources for Human Development... ...Join a Mission-Driven OrganizationWhat You'll DoAs a Clinical Coordinator, you will:Maintain up-to-date knowledge and implementation of...Work experience placementLocal area$143.01k - $168.47k
...have the right talent, at the right time, in the right way.The Clinical Trial Manager is an experienced clinical operations... ...expectations, and operational deliverables are achieved.Lead and coordinate clinical trial start-up, maintenance, close-out, and inspection...Minimum wageFull timeWork at officeLocal areaFlexible hours$75k - $90k
Piper Companies is currently looking for an experienced Quality Control Biochemist in West Point, Pennsylvania (PA) to work for a leading pharmaceutical manufacturer. Responsibilities for the Quality Control Biochemist include: Utilize skills with HPLC (Empower), SDS-Page...- Johnson & Johnson Innovative Medicine seeks a Director of Clinical Research Oncology to lead the oncology program in a global, matrix environment... ...development, medical review, and regulatory submissions, coordinating with GCO, Data Management, and Regulatory functions. The...
- ...Job Description Job Description Clinical Manager (RN) – Home Health Montgomery PA Home Health (MPV) | Blue Bell, Pennsylvania BAYADA... ...Lead client assessments, care planning, case management, and coordination of care in accordance with physician orders, clinical...Full timeWork at officeLocal area
- Tower Health is seeking a qualified coordinator for clinical research studies. This role involves facilitating and overseeing research activities in both inpatient and outpatient settings, with a strong emphasis on regulatory document processing and interactions with sponsors...
- Phoenixville Hospital - Tower Health is seeking a candidate to coordinate and facilitate clinical research studies within multidisciplinary teams. The role includes overseeing study activities, processing and shipping specimens, and maintaining study documentation. Qualifications...
- ...for ophthalmology as ranked by U.S. News & World Report. Our clinical expertise, state-of-the-art diagnostic testing and advanced... ...Location: Plymouth Meeting, PA 19462 The Medical Records Coordinator is responsible for the routine preparation and maintenance of...Full timePart timeLocal areaWorldwide
- CSL Plasma Inc. seeks a Clinical Supply Manager to lead planning and management of clinical trial supplies for low to medium complexity... ...assistance are not provided. You will forecast drug volume, coordinate storage, redistribution, and collaboration with R&D and external...Relocation package
- ...3 days onsite weekly. Relocation and mobility assistance are not provided. Main Responsibilities Ensure efficient, cost-effective clinical trial supply planning and management for low to medium complexity studies Performs planning and forecasting of drug volume requirements...Relocation package
- CSL is seeking a Senior Clinical Trial Case Manager to lead end-to-end case management for global biotechnology and pharmaceutical studies. In this role, you will oversee case processing, data review, and safety documentation, ensuring accuracy, patient safety, and adherence...
- ...a hybrid onsite professional in King of Prussia, PA to manage clinical trial supply planning for low to medium complexity studies. The... ...and archiving, and support continuous improvements while coordinating with cross-functional teams and external service providers. #J...
- Acts as Case Management subject matter expert in cross-functional teams for assigned clinical trials. Manages case management activities for assigned clinical studies to ensure compliance with national and international regulations, such as GxP guidelines and/or other...Local area
- Overview Acts as case management subject‑matter expert in cross‑functional teams for assigned clinical trials, managing case management activities to ensure compliance with national and international regulations, GxP guidelines, and company policies. Oversees the delivery...Local area
$282.2k
...Implementation (V&I) organization, which includes GMSA as well as Outcomes Research.The GDMA is a subject-matter expert (SME) in their area of... ...representative within Product Development sub-teams (including Clinical, V&I, Commercial, Publications, and Label), leveraging the V&I...Full timeFor contractorsLocal areaFlexible hours$190.8k - $300.3k
...connecting technology investments to measurable business results.As AI rapidly reshapes pharmaceutical R&D — from molecule discovery and clinical trial design to regulatory intelligence and real-world evidence — we need strategic technology leadership more than ever. We are...Full timeFor contractorsLocal areaVisa sponsorshipFlexible hours$18.02 - $21.63 per hour
...Center with a welcoming demeanor. Must have general clerical skills and attention to detail. Competent skillset with EHR and other clinical software. Ability to demonstrate professionalism, knowledge of medical terminology is preferred. Must be willing to conduct...Full timePart timeImmediate startMonday to FridayFlexible hours- ...with the executive of the entire process of drug development/ clinical trials. Plainsware or any project planning software experience... ...to plan accordingly. Position Overview: • The Manager, Program Coordination provides coordination support to the Clinical functional teams...Work experience placement
$199k - $343.85k
...diversity and dignity of our employees and recognize their merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function: Clinical Development & Research - MDJob Category:Scientific/TechnologyAll Job Posting Locations:Spring House, Pennsylvania, United...Full timeContract workWork experience placementImmediate start$73.2k - $89.5k
...right talent, at the right time, in the right way. The Clinical Data Coordinator is responsible for supporting the collection, management,... ...experience in clinical data management or a related clinical research role within the pharmaceutical or biotechnology industry....Minimum wageFull timeWork at officeLocal areaFlexible hours- ...Medical DirectorICON 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 are at the heart of...
- ...Responsibilities The Horsham Clinic is seeking a dynamic and talented Environmental Service Aide The Horsham Clinic is a 2... ...Clinic. Visit us online at Summary : The Staffing Coordinator is responsible for coordinating the scheduling needs of nursing...Summer holidayLocal areaShift work
$85k - $93k
...-being of our patients and residents while making a meaningful impact in the communities we serve. Responsibilities: The MDS Coordinator - RN is responsible for the timely and accurate completion of the MDS treatment assessment tool and for reviewing care plans and...Temporary workImmediate start
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