Remote Clinical Research Specialist
70% of an average work week, so about 28 hours/week.
Preferably working from New Haven, CT.
Contractor will need to train onsite and then be able to work remote
Job description:
• 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.
Bachelor’s degree Engineering/ (B.A./B.S.C./Other)
Experience required:
0-2 years
Feel free to forward my email to your friends/colleagues who might be available. We do offer 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
Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Direct: (732)-429-1649
Tel: (732) 549 2030 x 230
Fax: (732) 549 5549
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Preferably working from New Haven, CT.
Contractor will need to train onsite and then be able to work remote
Job description:
• 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.
Bachelor’s degree Engineering/ (B.A./B.S.C./Other)
Experience required:
0-2 years
Feel free to forward my email to your friends/colleagues who might be available. We do offer 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
Inc. 5000 - 2007, 2008, 2009, 2010, 2011, 2012 ,2013 and 2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Direct: (732)-429-1649
Tel: (732) 549 2030 x 230
Fax: (732) 549 5549
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.