Clinical Research Associate II/Sr. CRA
ICON
CRA II/Sr. CRA- Detroit, MI 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 CRA II 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: You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Collaborating with investigators and site staff to facilitate smooth study conduct. Performing data review and resolution of queries to maintain high-quality clinical data. Contributing to the preparation and review of study documentation, including protocols and clinical study reports Your Profile: You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience: Bachelor's degree in a scientific or healthcare-related field. Minimum of 2 years of experience as a Clinical Research Associate. In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. Strong organizational and communication skills, with attention to detail. Ability to work independently and collaboratively in a fast-paced environment. Willingness to travel as required (approximately 60%) 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. 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
$96.2k - $151.4k
...in a country.Under the oversight of the CRA-Manager the person ensures compliance... ...site manager throughout all phases of a clinical research study, taking overall responsibility of... ...Regulations, Protocol, Site Monitoring Plan and associated documents.Gains an in-depth...SuggestedFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week- ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...mission to shape the future of clinical development. As a CRA II at ICON, you will design and analyse clinical trials, interpreting...Senior
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- ...design, administration and monitoring of clinical trials. Responsibilities: Plans,... ...Collects, prepares and maintains required research documentation, such as informed consent... ...with 2 years of cumulative experience OR Associate degree/Technical degree OR 4 years of applicable...Shift workDay shift1 day per week
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$71.9k - $189k
Clinical Research Associate, Sponsor Dedicated Warren, United States of America | Full time | Field-based | R1541733 To be eligible for this position, you must reside in the same country where the job is located. Essential Functions Perform site monitoring visits (selection...Full timePart timeLocal area- ...Detroit seeks a candidate to participate in the design, administration and monitoring of clinical trials. The role involves supporting daily project protocols and essential research documentation, including informed consent records and medical reports. Responsibilities...
$19.26 - $24.6 per hour
...Title: Automotive Laboratory Technician I or II Location: Dearborn, MI Zip Code: 48120... ...I will support engineering testing for research, development, or certification of... .... Education and Experience (preferred) Associate degree or Technical School certification....Local areaImmediate start- Merck & Co. is seeking an experienced clinical research professional to manage assigned sites, ensure adherence to ICH‑GCP, and drive site expansion across selected regions. You will act as a primary site contact and oversee monitoring throughout all trial phases. Qualified...Remote job
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$150k - $200k
Sr. Manager/Principal - Audit & AssuranceJoin an established, highly respected public accounting firm in Michigan where a $150,000-$200,000 salary, senior-level autonomy, and executive leadership are waiting for a seasoned audit professional ready to drive practice growth...SeniorFull time- ...develops, tests, implements, and supports clinical and administrative data interfaces... ...technical analytical skills to seek out, research and evaluate a variety of solutions to provide... ...certification (or higher), Cloverleaf Level II certification, Cloverleaf version 5.8 or...SeniorWork experience placement
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$1,367 - $1,528 per week
Medical Laboratory Technician Location: Detroit, MI Agency: Prime Time Healthcare Pay: $1,367 to $1,528 per week Shift Information: Rotating - 5 days x 8 hours Contract Duration: 13 Weeks Start Date: ASAP About the Role: Prime Time Healthcare...Full timeContract workSummer workImmediate startShift workRotating shift$1,351 - $1,392 per week
..., and unique cultural attractions during your assignment. AMN Healthcare provides excellent compensation, dedicated recruiters, a clinical support team, and the AMN Passport app for 24/7 career management. As a publicly traded company, AMN Healthcare upholds high ethical...Hourly payWeekly payExtra incomeFull timeContract workTemporary workImmediate startShift workNight shift$28.85 - $50.24 per hour
...notification timing, adverse action accuracy, and procedural adherence, and recommends enhancements. Analyzes Community Reinvestment Act (CRA) performance for applicable state-based requirements, including data requirements, performance analysis including demographic parity,...Senior- A clinical research organization is seeking an Assistant Clinical Research Coordinator to support the coordination and execution of clinical trials. This role will involve patient recruitment, data collection, and ensuring adherence to study protocols while maintaining...Remote job
- Profound Research LLC in Detroit, Michigan, is seeking an Assistant Clinical Research Coordinator. You’ll support high-volume vaccine clinical trials, gaining hands-on experience in study coordination and clinical procedures. This 1099 contract can lead to a full-time role...Full timeContract work
$21 - $25 per hour
Flourish Research in Detroit, MI is seeking a Research Assistant to support our clinical trials team at the Detroit site. This full-time, on-site role follows regular Monday-Friday business hours and offers a compensation of $21 to $25 per hour. Key functions include assisting...Hourly payFull timeMonday to Friday- ...as fine needle aspirations. General interpretation overview of clinical cases as well as correct determination of appropriate auto... ...High school diploma or equivalent required. Bachelor's/associate degree (biology, chemistry/histology) or completion of laboratory...SeniorFull timeShift workWeekend work
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