What are the responsibilities and job description for the Clinical Research Assistant position at Insight?
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.
Benefits for our Full Time Team Members:
- 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.
Duties and Responsibilities:
- 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
Qualifications:
- 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!