Clinical Trial Assistant

Adecco- Medical& Science is recruiting talented individuals to join a rapidly growing clinical research organization conducting studies at the forefront of novel technologies for disease diagnosis and biomarker discovery projects such as the baseline study. Candidates for the role of Clinical Trial Associate (CTA) should have-2 years experience supporting clinical trial operations and demonstrated interest in working on innovative approaches to transform our understanding of human health, particularly the detection of early transitions from health to disease.

CONTRACT DURATION- 1 year

RESPONSIBILITIES:

-The primary role of the CTA is to support the logistical aspects of clinical trial conduct in compliance with Good Clinical Practice (GCP) and relevant Standard operating procedures (SOP's)
-The CTA will working closely with other members of the Clinical Team, specifically in activities of study set-up, conduct a clinical studies, including: Support the Clinical Team by accurately updating and maintaining clinical systems that track site compliance and pnd completion Performance within project timelines.
-Assist in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to SOPs and study requirements, as well as periodic review of study files for accuracy and completeness.
-Support the preparation, handling and distribution of Clinical Trial Supplies related to biospecimen collection, processing, shipment, and storage, as well as maintenance of associated tracking information and management of external vendors.
-Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow. Facilitate internal project communications, correspondence and associated documentation.


MINIMUM QUALIFICATIONS:

-BA/BS degree 1-2 years of work experience in operations, clinical research or relevant field preferred qualification: Knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines preferred Experience supporting clinical study operations, including studies involving development of therapeutics, medical devices, or diagnostics Familiarity with sample management, sample processing, and biobanking best practices Computer skills including proficiency in use of Microsoft Word, Excel, PowerPoint and Google Docs.
-Strong written and verbal communication skills ,effective time management and organizational skills attention to detail and accuracy in work ability to establish and maintain effective working relationships with coworkers, managers and clients
-School diploma/certificate or equivalent combination of education, training and experience; BS/BA preferred

To be considered for this position, please use the "apply now" button to submit your resume. If you have questions about the position please contact Ankita Singh at Ankita.Singh@adeccona.com or call at 650-745-0052 #LI-AS1

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Reference number US_EN_2_108218_330856