Clinical Research Technician II — Trial Operations & Mentorship
CareAbout
Altasciences is seeking a Clinical Research Technician II to support clinical trial activities, ensuring GCP/SOP compliance and confidentiality of participants and sponsors. The role includes handling specimens, processing, and coordinating with clinic teams in a fast-paced setting. Ideal candidates have a high school diploma or GED (college degree preferred) and strong customer service skills; bilingual abilities are a plus for Montreal locations. #J-18808-Ljbffr CareAbout
Vacancy posted 3 days ago
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- About The Role The Clinical Research Technician II will work with Clinic teams to execute clinical trial activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. Schedule: Monday - Friday 08:00-16:30 OR 09:00...OperationsMonday to Friday
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Overland Park, KS5 days ago- Washington University in St. Louis invites applications for a Clinical Research Study Assistant II in Neurology. This on-campus role supports a team of... ...consent, and enroll participants in industry-sponsored trials focused on MS and related neurological conditions....Suggested
- ...overnight, weekend shifts About The Role The Clinical Research Technician I will work with Clinic teams to execute clinical trial activities in compliance with study... ...Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s. What You'll Do Ensure the...OperationsShift workNight shiftDay shiftAfternoon shift
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Overland Park, KS1 day ago $35.8k - $123k
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Overland Park, KS17 hours ago- ## Clinical Research Study Assistant II - NeurologyApplyremote type: On Campus/Onsitelocations: Washington University Medical Campustime type: Full timeposted... ..., Professor of Neurology, as well as with a clinical trial research team of over 10 research coordinators and a...Work experience placementWork at office
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Stilwell, KS18 hours ago - Altasciences is hiring a Clinical Research Technician I to support clinical trial activities across teams, ensuring compliance with study protocols, GCP, and... ...collaborate with supervisors to uphold quality. A path to mentorship and ongoing training is provided. #J-18808-Ljbffr...Flexible hours
$90.2k - $197.5k
Role Overview: As a Clinical Research Associate, you’ll be at the forefront... ...of ensuring our study sites operate smoothly and efficiently.... ...essential documents in the Trial Master File (TMF) and Investigator... ...per regulatory requirements.Mentorship: Mentor clinical staff...Full timePart timeWork at officeLocal areaImmediate startWorldwideIQVIA
Shawnee Mission, KS4 days ago$71.9k - $189k
Job Overview:Join our dynamic team as a Clinical Research Associate! You’ll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols... ..., and other necessary documentation.Mentorship: Mentor clinical staff through co-...Full timePart timeWork at officeLocal areaImmediate startWorldwideIQVIA
Shawnee Mission, KS18 hours ago- ...commercialization, offering expertise in regulatory strategy, clinical trial design and execution, market access, and post-market... ...Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and...Local area
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...utilize your skills, knowledge, and clinical judgement to provide a high... ...for participants in clinical trials and respond to emergency situations based upon clinical research standards. Responsibilities... ...sit for extended periods and operate a vehicle safely....Work at officeLocal areaNight shift- ## Clinical Research Study Assistant II - Obstetrics and GynecologyApply: On Campus/Onsite: Washington University Medical Campus: Full time: Posted Today: JR97776# **Location**SAINT LOUIS, MO 63108# **Scheduled Hours**40# **Position Summary**Under the direction of a Research...Full timeWork experience placementWork at office
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Lenexa, KS2 days ago - ...Clinical Research Associate, Sponsor DedicatedPerform monitoring and site management work to ensure that sites are conducting the study(ies... ...(as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File...Local area
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Overland Park, KS4 days ago $71.9k - $189k
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...and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference... ...are available for filing in the Trial Master File (TMF) verify that the Investigator... ...and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical...Full timePart timeLocal areaImmediate startWorldwideIQVIA
Shawnee Mission, KS9 hours ago$90.2k - $175.1k
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Overland Park, KS1 day ago- Lab technician, Quality Control (QC), Administrative Assistant Eurofins... ...and in the support of clinical studies. In over 35 years, Eurofins... ...by management. Level II - Fully meets the qualifications... ...understanding of Laboratory operations. Level III - Fully meets the...OperationsFull timeWork at officeVisa sponsorshipWork visaWeekend workAfternoon shift
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