Candidate Solutions

Search Jobs

  • Share this Job

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.


Powered by AkkenCloud