Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Summary:
The Center for Veterans Research and Education (CVRE), whose mission is helping to support innovative research
and education initiatives that improve the health and well-being of Veterans, is seeking a Clinical Research
Assistant I. The part-time dermatology Clinical Research Assistant I will be hired to primarily work on the
DermoSight project and other VA funded grants. The CRA I will work closely with Dr. Goldfarb, working with
patients and working on publications.
Responsibilities: Major duties and responsibilities may include, but are not limited to the following:
Obtaining informed consent
Giving patient instructions
Gathering medical and medication histories for study participants
Conducting study participant follow-up
Publish original articles, with assistance.
Other duties as assigned
Applicants must include a cover letter.
Minimum Qualifications:
Education: Bachelor’s (BA/BS) or above from an accredited college or university in
public health, sociology, psychology, or related allied health field
Experience: Prior research experience (1 year) is preferred, but not necessary.
Licensure/Registration/Certification: None
Preferred Qualifications:
Research Assistant experience dealing with data collection and data storage, human subject studies, and
institutional review board processes.
Knowledge of Good Clinical Practices, human subjects’ protections, and federal regulations related to
clinical research.
Prior research experience is preferred, including data collection and data storage, human subjects’ studies,
and institutional review board process.
Familiarity with REDCap is preferred.
Some programming knowledge
Knowledge, Skills and Abilities:
Basic experience with trouble-shooting devices and software settings.
Experience in coordinating multiple task and project elements with differing timelines and completion
deadlines.
• Demonstrated ability to work effectively both independently and as part of a team.
• Excellent oral and written communication skills.
• Exceptional attention to detail and organizational skills.
DocuSign Envelope ID: 14033A5AD0905907-5F910747--44101304--ABF0D5E0-9D1C1292E891AABA304DE32D
Conditions of Employment:
• Subject to a criminal and educational background check.
• Designated and/or random drug testing may be required.
• Regular and predictable attendance is required.
• Typical hours fall within standard business hours, work may be required during hours beyond standard business hours, including weekends.
• Must be a US citizen
Physical Requirements: The employee must be able to navigate the medical center, use a keyboard, and life up to 25 lbs. Reasonable accommodation may be considered in determining an applicant’s ability to perform the duties/functions of the position.