Clinical Research Specialist

Integrated Resources Inc.; New Haven (CT); Hybrid; USD 60,000 - 85,000; Full time

Job summary

Integrated Resources Inc. is seeking a contractor to support clinical trials involving pill cam procedures. The role includes providing training, coordinating logistics, and ensuring compliance with clinical standards. Candidates should possess a relevant bachelor’s degree and experience in clinical trial management. The position requires onsite training for three months with the possibility of remote work thereafter.

Qualifications

• Bachelor’s degree in relevant fields.
• Experience in managing trial logistics and support.
• Strong attention to detail and data integrity.

Responsibilities

• Provide product training and support for clinical sites.
• Coordinate logistical aspects of clinical trials.
• Ensure compliance with regulations and integrity of data.

Skills

Clinical trial management

Data integrity

Patient safety

Logistics coordination

Education

Bachelor’s degree in Engineering, B.A., B.S.C., or other relevant fields

Job 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.
• Arrange and participate in the organization of study team meetings, take minutes, and distribute.
• 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 any clinical trial databases/tracking tools are set up and maintained throughout the trial.
• Assist with collating, tracking, and shipping CRFs & data queries to data management.
• Review and approve monitoring reports in Siebel.
• 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.
• Ensure the integrity of data reported.
• Assist in setting up the study centers, including ensuring each center has the trial materials and training site staff to trial-specific standards.
• Provide administrative support for the CA and data management team, including shipment, training records, and inventory control.

Qualifications

Bachelor’s degree in Engineering, B.A., B.S.C., or other relevant fields.