Clinical Trial Associate

Adecco-Medical & Science is looking for a Clinical Trial Associate for one of our leading biotech clients in South San Francisco.


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 (SOPs).

Responsibilities:

Recruit, schedule, and consent clinical study subjects
Assist in the preparation, handling, distribution, filing, and archiving of clinical study documentation • Accurately maintain Trial Master File documentation to ensure audit readiness
Support the preparation, handling, tracking, and distribution of Clinical Trial Supplies
Assist with the completion, tracking, and management of Case Report Forms (CRFs), data queries, and clinical data flow
Support monitoring visits and resolve monitoring findings
Assist Clinical Operations team members with study-related duties as necessary Minimum


Qualifications:

BA/BS degree
2 years of experience in clinical research
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
Computer skills including proficiency in use of Microsoft Word, Excel, PowerPoint and Google Docs


Preferred Qualifications:

Graduate-level degree or RN

Working knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines


Interested candidates can apply now or send your updated resumes at ankita.singh@adeccona.com or can call at 650-745-0052.


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Reference number US_EN_2_108218_332157