Clinical Research Coordinator II - Neurology
$54,600.00 - $81,900.00 / Annually
You'll complete your application on the employer's website.
$54,600.00 - $81,900.00 / Annually
You'll complete your application on the employer's website.
Job type
Salary
$54,600.00 - $81,900.00 / Annually
Location
Sector
Posted
27 days ago
Location SAINT LOUIS, MO 63110 Scheduled Hours 40 Position Summary Serve as a coordinator in The Life-space, isolation, and functional exposome study in preclinical Alzheimer's disease and cognitive environments (LIFESPACE) project. The coordinator is responsible for providing day-to-day operational leadership, financial organization, compliance, budgeting, participant recruitment, and data collection for the project. The coordinator acts as a liaison between the PI and other study components, the school, personnel, collaborators, the sponsoring agency, and study participants. The coordinator is responsible for managing all phases of study protocol as required by the PI and sponsoring agency(s) to ensure compliance, providing supervision of administrative support for the laboratory, and managing prospective and current grants. The coordinator participates in the strategic planning and overall development of the laboratory. Job Description Primary Duties & Responsibilities: Works closely with Senior Coordinator for management of day-to-day operation of the study. Implements and manages protocols. Identifies problems or inconsistencies. Addresses complaints and/or needs of participants, staff, or partners. Prepares reports and gives presentations both internally and externally as requested by the PI. Establishes excellent rapport with research participants, staff, and partners. Obtains informed consent for study participation and administers study tests and questionnaires to research participants using standardized protocols. Complete blood draws. Works closely with other coordinators to manage participant scheduling and records. Oversees entry of study data. Assists with grant preparation, compliance, and progress reporting. Writes non-scientific portions of grant, as needed. Communicates with Neurology grants specialists and coordinates grant submission. Under the direction of the PI, manages laboratory resources, including staff, facilities, equipment, and budgets to meet the laboratory’s goals and objectives. Ensures coordination and maintenance of equipment and supplies. Supervises federal work-study employees and/or students as needed. Aids in the development of forms, questionnaires, and the application of research techniques. Assists in writing, maintaining, and updating procedure manuals. Plans for future needs. Submits documents for IRB approval and prepares appropriate modifications. Oversees continuing review process, resolves IRB protocol management issues, and recommends corrective action. Performs other duties as assigned. Working Conditions: Job Location/Working Conditions Patient care setting. Physical Effort Typically sitting at desk or table. Equipment Office equipment. The above statements are intended to describe the general nature and level of work performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all job duties performed by the personnel so classified. Management reserves the right to revise or amend duties at any time. Required Qualifications Education: Bachelor’s degree or combination of education and/or experience may substitute for minimum education. Certifications/Professional Licenses: The list below may include all acceptable certifications, professional licenses and issuers. More than one credential, certification or professional license may be required depending on the role. Basic Life Support - American Heart Association, Basic Life Support - American Red Cross Work Experience: Clinical Research (2 Years) Skills: Not Applicable Driver's License: A driver's license is not required for this position. More About This Job Required Qualifications: Basic Life Support certification must be obtained within one month of hire date. Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirement). Preferred Qualifications: Significant interest in clinical/translational research and training with an authentic aspiration to support those missions. Experience with funding agencies and aspects of academic grant management including accurate reporting of data and compliance with requirements of government agencies. Enjoys working with older adults (65+ years). Has experience with phlebotomy or willing to undergo training to complete blood draws. Preferred Qualifications Education: No additional education unless stated elsewhere in the job posting. Certifications/Professional Licenses: No additional certification/professional licenses unless stated elsewhere in the job posting. Work Experience: No additional work experience unless stated elsewhere in the job posting. Skills: Clinical Research, Clinical Study Protocols, Database Management, Research Projects, Spreadsheet Analysis, Statistical Analysis Software (SAS)
Interested in this role?
Apply directly on the employer's website — it only takes a few minutes.
Other roles in Remote or Science & Pharmaceutical
Competitive
You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…
When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.
$21.64 - $26.50
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.