About this role

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Contractor will need to train onsite for 3 months and then be able to work remote.

· Provide product training and support to clinical sites for the pill cam procedure.

· Support the randomization process and act as the IWRS PRIMARY Administrator

· Arranging and participating in the organization of study team meetings Taking minutes and distributing

· Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop, IWRS User information.

· Administer, Maintain and coordinate the logistic aspects of clinical trials according to GCP and Sop’s

· Ensure That any clinical trial databases/tracking tools are set up and maintained throughout the trial

· Assist with collating, tracking & shipping CRFs & Data queries to data management

· Maintaining study data control table

· Review and approve monitoring reports in Siebel

· CTM SW update

· Coordinating archiving of study documentation

· Perform and support study site qualification, Initiation interim monitoring and closeout visits according to SOP’s GCP’s, FDA regulation and ICH guidelines at multiple investigational sites

· Ensure safety and welfare of Patient enrolled in clinical study

· Site management to ensure Compliance

· Ensure integrity of data reported

· Helping in setting up the Study centers, Which includes ensuring each center has the trial materials and training site staff to trial-specific standards

· Administrative support for CA and date management team including: shipment training records and inventory control.

Qualifications

Bachelor’s degree Engineering/ (B.A./B.S.C./Other)

Experience required:

0-2 years

Additional Information

Kind Regards,

Sasha Sharma

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - 732-662-7964

Frequently Asked Questions

Is the salary disclosed for the Clinical Research Specialist position at integratedresourcesinc?
The salary for this Clinical Research Specialist role at integratedresourcesinc is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
Where is the Clinical Research Specialist position at integratedresourcesinc located?
This Clinical Research Specialist role at integratedresourcesinc is based in CT, New Haven, New Haven, CT, United States, us. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
Is the Clinical Research Specialist role at integratedresourcesinc full-time or part-time?
This is listed as a Full time position. It is posted as a Clinical Research Specialist role at integratedresourcesinc.
How do I apply for the Clinical Research Specialist position at integratedresourcesinc?
Click the "Apply Now" button on this page. You will be redirected to integratedresourcesinc's official application portal hosted on smartrecruiters where you can submit your application directly.
When was the Clinical Research Specialist job at integratedresourcesinc posted?
This Clinical Research Specialist position at integratedresourcesinc was posted on Jan 18, 2017. Apply as soon as possible — early applications are often reviewed first.
Clinical Research Specialist
integratedresourcesinc
Apply for this role ↗

You'll be redirected to integratedresourcesinc's official application page on SmartRecruiters.