Clinical Research Coordinator
Reliance Clinical Testing Services, Inc.
At ALS, we encourage you to dream big. When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. About the role ALS global company, is a leader in the field of clinical testing with an opening for full-time Clinical Research Coordinator (CRC) in Phoenix, AZ. The successful candidate will join a team that provides clinical testing services to many of the world's best-known consumer product companies. Responsibilities Duties include but not limited to: Plans, develops, and coordinates the safety and efficacy research studies under the supervision of the Principal Investigator and in accordance to protocol, company SOP’s and Good Clinical Practices. Participates and coordinates the planning, development and implementation of clinical protocols, logistical procedures, and operating systems in accordance with parameters set out by the study sponsor and Principal Investigator. Supervises, evaluates, and coordinates the activities of a team of Clinical Research Assistants; ensures that all clinical activities are carried out in accordance with Company SOP's and guidelines of Good Clinical Practices. Oversees the planning, scheduling, and carrying out of day-to-day clinical activities, maximizing on study workflow, and associated availability of research subjects. Works closely with Recruitment Department ensuring specific research subject entrance criteria is observed prior to conducting study. Monitors test subjects’ response to treatment and communicates study data and results to investigators in a timely fashion. Works in conjunction with Clinical Management on generation of protocols, interim reports, and final reports for Company sponsors. Order and maintain inventory of laboratory supplies. Other duties as assigned. About you Bachelor of Science or Arts degree in life sciences preferred. 1 – 2 years’ experience in clinical industry experience (substitute for BS or BA). Working conditions Sitting and/or standing for extended periods of time, up to eight (8) hours per business day Must be able to stand, bend, push, pull, stoop and crouch frequently while performing the duties of this position Must be able to lift (with both hands) and/or move up to 50 pounds and occasionally lift and/or move heavier loads with assistance Must be able to interact and communicate effectively with panelist Working at ALS The ALS team is a diverse and dedicated community united by our passion to make a difference in the world. Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence. At ALS, you’ll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities. But most importantly, our people care – for each other and for the work we do. With over 20,000 team members across 70 countries, you’ll be part of a global network. Everyone Matters ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy‑related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities. ALS also welcomes applications from people with all levels of ability. Reasonable adjustments to support candidates throughout the recruitment process are available upon request. Eligibility To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa. #J-18808-Ljbffr Reliance Clinical Testing Services, Inc.
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- ...The Clinical Research Coordinator I will work at site to help ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor...SuggestedFull time
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Join Valleywise Health and elevate your clinical research career! As a Clinical Research Coordinator II , you will champion our prospective specimen collection research studies from concept to execution. Working under the guidance of our Program Manager of Academic...SuggestedWork at office- ...A will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations... .... Adherence to ALCOA-C Standards with all the relevant clinical trial documentation. Completing and overseeing data entry and...Full time
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- Mayo Clinic in Phoenix/Scottsdale seeks a study coordinator to manage non-therapeutic clinical research protocols under PI supervision. The role involves coordinating protocol logistics, data collection, and regulatory duties to ensure compliant study conduct. The ideal...
- Axsendo Clinical Research is a rapidly growing, multi‑market clinical research organization specializing in Neurology, Cardiology, Metabolic... ...we are seeking a skilled, service‑mindful Clinical Research Coordinator II to join our team. Position Overview The Clinical...
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- Privacy Policy Job Openings Clinical Research Coordinator Clinical - Phoenix, Arizona Department Clinical Employment Type Full-Time Minimum Experience Experienced TL;DR As a Clinical Research Coordinator, you have mastered the art of multitasking, prioritizing, and efficiency...Full timePrivate practiceWork at officeLocal areaFlexible hours
$58k - $68k
...Job Description Job Description Clinical Research Coordinator Required Qualifications Minimum 2 years of experience as a Clinical Research Coordinator required. Hands-on phlebotomy experience required. Experience working directly with patients in a clinical...Permanent employmentFlexible hours$27.5 - $36 per hour
...advancing medical innovation through leading clinical trials, ensuring patient safety and... ...network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites... ...qualified candidates for the Clinical Research Coordinator II or III position in Peoria Title...Hourly payFull timeTemporary workLocal areaMonday to Friday- ...investigator supervisor or other staff involved in research protocol(s). Gives direction to and works... ...Non-Essential Functions): Independently coordinates complex (i.e. interventional therapeutic greater than minimal risk) clinical research protocols with minimal direction...Full timeInternship
$53.04k - $66.3k
...Clinical Research Coordinator II, Department of Neurosurgery (COM-P) Posting Number req27152 Department COM Phx Campus Administration Department Website Link Location Greater Phoenix Area Address Phoenix, AZ USA Position Highlights The...Full timePart timeWork experience placementWork at officeLocal areaRelocationFlexible hours- ...Surgery-Clin Work Shift: Day Job Category: Research Great options and opportunities. We’re certified as... ...in advancing orthopedic care through innovative clinical research. As a Clinical Research Coordinator, you'll collaborate with physicians, patients, and...Full timeMonday to FridayShift work
- Phoenix Children's Hospital, Inc. in Phoenix, AZ is seeking a Research Studies Coordinator to oversee psychology research projects from startup... ...role requires collaboration with principal investigators and clinical teams to ensure accurate documentation, IRB compliance,...Full timeDay shift
- Alliance Clinical Network is seeking a Clinical Research Coordinator to support the conduct of clinical trials at our Phoenix, AZ site. You will coordinate study visits, manage data collection, ensure regulatory compliance, and interact directly with participants to uphold...
- MissionHires is seeking a Clinical Research Coordinator in Phoenix, Arizona, who is fluent in Spanish and eager to grow within a dynamic clinical trial environment. The Coordinator will manage daily clinical trial operations, ensure regulatory compliance, and communicate...
- Clinical Research Coordinator III - Thunderbird Office Arizona Kidney Disease and Hypertension Center (AKDHC) is one of the nation’s largest groups of physicians specializing in the care of patients with renal disease. Since 1976, we have enjoyed the trust of patients and...Work experience placementWork at office
- Dm Clinical Research Group in Phoenix, AZ seeks an experienced Clinical Research Supervisor to oversee site activities, ensure GCP compliance... ...enrollment. You will train staff, monitor data quality, and coordinate with cross-functional teams to meet sponsor expectations....
- DM Clinical Research Group in Phoenix, AZ is seeking a Clinical Research Coordinator I to join our site and ensure high-quality data collection in line with sponsor protocols, FDA regulations, and ICH/GCP guidelines. You will help enrollment meet sponsor expectations and...
$65.69k - $85.39k
Clinical Research Coordinator IV, Department of Internal Medicine - Cardiology (Phoenix) The Department of Internal Medicine at The University of Arizona College of Medicine -Phoenix, invites candidates interested in a rapidly growing career as a Clinical Research Coordinator...Full timePart timeWork experience placementWork at officeLocal areaFlexible hoursWeekend work$26 - $38.55 per hour
Mayo Clinic in Phoenix, Arizona is seeking a Clinical Research Coordinator to oversee non-therapeutic clinical research protocols. This full-time position requires coordinating schedules, monitoring research activities, and ensuring compliance with regulatory laws. The...Hourly payFull time- Phoenix Children's is seeking a Clinical Research Coordinator to manage diverse oncology-related studies. The role involves coordinating pre-study through study closure, data extraction, and meticulous regulatory documentation while working with investigators and care teams...
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