Clinical Research Assistant

Insight-posted 12 days ago

Full-time • Entry Level

Onsite • Flint, MI

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Insight Institute of Neuroscience & Neurosurgery (IINN) aims to advance, challenge, and revolutionize neurosciences and medicine through scientific research and advanced technology, driven by a passion to help others regardless of any obstacles and challenges that may lie ahead. Our integrated team of medical professionals does so through creative, innovative techniques and care principles developed because of our continuous pursuit to improve the field of medicine. Our integrated team works together to find solutions to both common and complex medical concerns to ensure more powerful, reliable results. Having multiple specialties “under one roof” Insight achieves its purpose in providing a comprehensive, collaborative approach to neuromusculoskeletal care and rehabilitation to ensure optimal results. Our singular focus is Patient Care Second to None! Job Summary: We are seeking competent, proactive, self-directed individuals with effective time management skills to assist our clinical research site. The Clinical Research Assistant will support the clinical research team at our Research Dearborn location . They will work under the direction of the Clinical Research Manager . Job Type: Full time (on-site, in-person) Monday to Friday, Full-time (8 hours), 8am - 5pm EST Ability and willingness to commute between our research locations as needed per study tasks Professional references may be required.

Schedule visit appointments after coordination with relevant parties
Coordinate collection, processing and shipping of study specimens
Assemble study kits for study visits
Attend and participate in study meetings, SIVs, monitoring visits and other sponsor and regulatory meetings
Complete Data Entry for studies both in sponsor EDC and CTMS
Ensure all paper sources are filed and securely kept in the binders
Assist and work closely with the Clinical Research Coordinator and Clinical Research manager in executing and monitoring the overall clinical study to ensure compliance with protocol
Report any adverse events according to the study protocol
Identify and assist in pre-screening potential subject leads
Assist in marketing the active trials in the community
Actively meet with investigator and study team to discuss study progress/status
Provides administrative updates on enrollment and queries if any
Other duties as needed per assigned study protocol

Ability to demonstrate authorization to work in the U.S. for any employer
Bachelor's degree or equivalent training required via work experience or education
At least one year of previous job-related experience preferred
Ability to follow oral and written instructions and established policies and procedures
Ability to analyze and interpret data
Ability to finish tasks in a timely manner
Ability to maintain accuracy and consistency
Ability to maintain confidentiality
Ability to work as an effective team member
Knowledge of medical terminology
Ability to function independently and manage their own time and work tasks
Diligent, thorough in their tasks, and show their commitment to their job
Insight is an equal opportunity employer and values workplace diversity!

Comprehensive health, dental, and vision insurance coverage
Paid time off, including vacation, holidays, and sick leave
401K with Matching; offerings vested fully @ 3 months of employment paired with eligibility to contribute
Short & Long Disability, and Life Term insurance, complementary of Full Time Employment
Additional Supplementary coverages offered @ employee's elections: Accident, Critical Illness, Hospital Indemnity, AD&D, etc.

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