Job detail

Clinical Research Technician I (CPT or MA)

CareAbout

#Customer Service #Confidentiality #Fast-Paced Environment #BLS #SOPs #CPT #MA #Clinical Research #GCP #Sample Handling

Quick overview

The Clinical Research Technician I will execute clinical trial activities in compliance with study protocols, Good Clinical Practices (GCP), and Standard Operating Procedures (SOPs). Responsibilities include sample handling, safety measurements, in-house testing, and maintaining high standards of customer service and safety.

Requirements summary

Candidates must possess a CPT or MA certificate along with a BLS certificate, and a High School Diploma or GED is required. A college degree and related work experience are preferred, along with good communication skills and a customer service focus.

high schoolprofessional certificateCommunicationCustomer ServiceStandard Operating ProceduresConfidentialityCPTBLSMAGood Clinical PracticesSample HandlingIn-house TestingQuestionnaire AdministrationClinical Trial ActivitiesSafety Measurements

Job description

Your New Company!
At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them.
No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe.
By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing team!
Whether you're a recent college graduate or seeking your next career opportunity, it's time to discover your future at Altasciences.
We are better together and together We Are Altasciences.
About The Role The Clinical Research Technician I will work with Clinic Operations teams to execute clinical trial activities.
Responsibilities of the Clinical Research Technician I include execution of What You'll Do Here/clinical activities in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOP)s.
What You'll Do Here Ensure the confidentiality of clinical trial participants and sponsors is respected.
Understand protocol driven timed study events and acceptable collection windows (protocol and/or SOP driven) for the timed events.
Report procedural deviations to appropriate supervisory team members.
Preparation and proper clean-up of applicable workstations (i.e. urine collection station, blood processing station, etc.) Maintain and advocate a high level of customer service, quality and safety within the department.
Perform clinical trial activities may include but not limited to, sample handling, safety measurements, in-house testing and questionnaire administration.
Conduct all clinical trial activities and participant interaction with a high standard of customer service.
Report significant participant misbehavior to Study/Clinical Operations management teams.
Provide feedback, where necessary, to appropriate team members of study progress.
Proactively communicate issues and/or problem resolutions to departmental supervisors and managers.
Complete and/or maintain training as required per jobs needs What You'll Need to Succeed CPT or MA certificate plus a BLS certificate required.

Clinical Research Technician I (CPT or MA)

2 listed locations

Quick overview

Requirements summary

Job description

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