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Clinical Trials Associate (CTA)

Location : Agoura-In Office
Job Type : Temp/Contract
Hours : Full Time
Required Years of Experience : 2
Required Education : BS or BA
Travel : No
Relocation : No

Job Description :

The Clinical Trial Associate (CTA) for Clinical Product Management will conduct, maintain and oversee activities related to investigational device and

clinical study medications.


§  Conduct and maintain investigational device accountability for all clinical studies.

§  As applicable, conduct and maintain study medication accountability for applicable clinical studies utilizing regulatory approved medication.

§  Generate and track device inventory and device shipments (and drug shipments as applicable).

§  Prepare study device for shipment(e.g., pack, label).

§  Facilitate orders and ship study device to/from the clinical sites.

§  Address and resolve discrepancies between site and ERP (sponsor’s tracking system) data on device accountability in collaboration with the global team.

§  Train sponsor staff and clinical site personnel on device accountability process, including within the electronic databases (e.g., ERP, e-Case Report Form).

§  Devise and/or revise procedures and/or workflows for process improvement.

§  Conduct and maintain other study product management (e.g., study supplies)as assigned by management.

Conduct ad hoc clinical research activities as assigned by management.









Required Qualifications :

Required Skills

§  Good computer skills in usage of MS Office Suite and Clinical Systems such as CTMS (Clinical Trial Management System), eTMF (electronic Trial Master file)and/or eCRF (electronic case report form) required.

§  Good understanding and knowledge of clinical device accountability,(preferred).

§  Good written and verbal communication skills and interpersonal relationship skills.

§  Good problem-solving and critical thinking skills.

§  Strict attention to detail.

§  Ability to manage competing priorities in a fast-paced environment.

§  Working knowledge of GCP/ICH guidelines.

Education and Experience

§  Bachelor's Degree(preferred) in are related field required and/or a minimum of 2 years of experience with previous clinical trial research required.

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