Integrated Resources Inc.
Remote Clinical Research Specialist
Integrated Resources Inc., New Haven, Connecticut, us, 06540
Integrated Resources, Inc. is a premier staffing firm recognized as one of the tri-state area's most well-respected professional specialty firms. Since its inception in 1996, IRI has built its reputation on excellent service and integrity. Our mission is to deliver high-quality talent, the first time and every time. We provide resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy, and Nursing.
Job Description
Work Schedule:
Approximately 28 hours per week (about 70% of a full-time schedule). Preferably based in New Haven, CT. The contractor will need to train onsite and then be able to work remotely. Provide product training and support to clinical sites for the pill cam procedure. Support the randomization process and act as the IWRS PRIMARY Administrator. Organize and participate in study team meetings; take minutes and distribute them. Manage and maintain study documents and trial supplies, including colonoscopy forceps, FedEx envelopes, and IWRS user information. Administer, maintain, and coordinate the logistical aspects of clinical trials according to GCP and SOPs. Ensure that clinical trial databases and tracking tools are set up and maintained throughout the trial. Assist with collating, tracking, and shipping CRFs and data queries to data management. Review and approve monitoring reports in Siebel. Update CTM software as needed. Coordinate archiving of study documentation. Perform and support study site qualification, initiation, interim monitoring, and closeout visits according to SOPs, GCPs, FDA regulations, and ICH guidelines at multiple investigational sites. Ensure the safety and welfare of patients enrolled in the clinical study. Manage sites to ensure compliance. Maintain the integrity of reported data. Assist in setting up study centers, ensuring each has the trial materials and trained staff to trial-specific standards. Provide administrative support for the clinical and data management teams, including shipment, training records, and inventory control. Qualifications
Bachelor’s degree in Engineering, B.A., B.S.C., or other relevant fields. Experience required:
0-2 years. Additional Information
Feel free to forward this email to colleagues who might be interested. We offer a referral bonus. Thank you for your time and consideration. I look forward to hearing from you! Warm regards, Nisha Integrated Resources, Inc. IT, Rehab, Clinical, Nursing Since 2007, 2008, 2009, 2010, 2011, 2012, 2013, and 2014 (8th Year)
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Work Schedule:
Approximately 28 hours per week (about 70% of a full-time schedule). Preferably based in New Haven, CT. The contractor will need to train onsite and then be able to work remotely. Provide product training and support to clinical sites for the pill cam procedure. Support the randomization process and act as the IWRS PRIMARY Administrator. Organize and participate in study team meetings; take minutes and distribute them. Manage and maintain study documents and trial supplies, including colonoscopy forceps, FedEx envelopes, and IWRS user information. Administer, maintain, and coordinate the logistical aspects of clinical trials according to GCP and SOPs. Ensure that clinical trial databases and tracking tools are set up and maintained throughout the trial. Assist with collating, tracking, and shipping CRFs and data queries to data management. Review and approve monitoring reports in Siebel. Update CTM software as needed. Coordinate archiving of study documentation. Perform and support study site qualification, initiation, interim monitoring, and closeout visits according to SOPs, GCPs, FDA regulations, and ICH guidelines at multiple investigational sites. Ensure the safety and welfare of patients enrolled in the clinical study. Manage sites to ensure compliance. Maintain the integrity of reported data. Assist in setting up study centers, ensuring each has the trial materials and trained staff to trial-specific standards. Provide administrative support for the clinical and data management teams, including shipment, training records, and inventory control. Qualifications
Bachelor’s degree in Engineering, B.A., B.S.C., or other relevant fields. Experience required:
0-2 years. Additional Information
Feel free to forward this email to colleagues who might be interested. We offer a referral bonus. Thank you for your time and consideration. I look forward to hearing from you! Warm regards, Nisha Integrated Resources, Inc. IT, Rehab, Clinical, Nursing Since 2007, 2008, 2009, 2010, 2011, 2012, 2013, and 2014 (8th Year)
#J-18808-Ljbffr