Clinical Research Specialist

Profile

What You Will Do:
Clinical Research Specialist
Full Time, 8-4:30pm
Baltimore, MD
Come elevate your skills and experience by working with a world class 800-bed, Magnet designated Academic Medical Center.
We are looking for a talented Clinical Research Specialist to join our Radiation Oncology Research team here at University of Maryland Medical Center.
Job Summary
Under general supervision, coordinates the implementation of research protocols approved for activation at the University of Maryland Medical System. Participates in complex clinical trial preparation and implementation; ability to work independently.
Submit protocols through appropriate review boards; assist in responding to queries; maintain proper communication with regulatory bodies Interface with relevant groups, industry sponsors, patients, physicians, or other members of the health care team.
Recruit and screen subjects for research studies.
Prepare studies for activation. Develop tools to assist in the proper study conduct, including cheat-sheets and manuals for various internal and external departments.
Perform clinical research activities per approved protocol including data collection, data entry, data verification, data analysis, compliance and clinical relevance of data. Conduct library research and contributes to the preparation and writing of research findings for publication of journal articles and grant proposals.
Perform administrative duties such as providing training and guidance to other clinical research staff.
Participate in the design of research studies
Anticipates and carries out independent actions necessary to provide competent and professional support to meet the needs of the faculty physicians, patients, administrators, co-workers, and others involved with clinical trials. Acts as a resource to investigators, faculty physicians and clinical research coordinators.
Acts as liaison between the institution and the study sponsor by preparing study reports and communicating with clinical study monitors.
Ensure that research is conducted according to Good Clinical Practices, Quality Assurance and Code of Federal Regulations.
Maintains clinical database(s) on patients participating in clinical studies and/or seen by a specific clinical service; periodically reviews data for compliance .
Oversees interaction with study participants, ensuring informed consent and compliance with protocol; monitoring subject symptoms; managing continuity of care.
Assists clinical investigator with study initiation, conduction, and completion.
Prepares and responds to audits conducted by study sponsors.
Represents department at research and protocol initiation meetings.
As a Team Member at UMMC
, you'll experience:
A supportive and collaborative work environment
A comprehensive benefits package including health, vision and dental coverage including prescription drug coverage, Tax-Free Savings Plans and more!
A highly competitive wage scale: Annual merit increases and a base wage scale that is measured against to market standards.
Generous tuition reimbursement of up to $5,000 per year for your graduate degree.
Located in downtown Baltimore near the Inner Harbor and Camden Yards, you won't find a more vibrant place to work!
What You Need to Be Successful:
Education and Experience
Bachelor's degree in epidemiology, sociology, psychology, nursing or field of study related to the research is required.
No experience is required.
May require training related to occupational safety and health, environmental compliance, shipping of hazardous materials and/or ionizing radiation.
At least 1 year of experience is preferred.
Knowledge, Skills and Abilities
Ability to understand and utilize scientific/medical terminology and research theory in both oral and written communications.
Ability to take a lead role in performing and directing various advanced, routine, and maintenance procedures.
Ability to perform independent projects and to serve as a consultant in area of technical specialty.
Ability to use measurable and verifiable information for making decisions or judgments.
Skill in statistical programming, interpretation and data analysis using statistical software as well as spreadsheet and database software applications.
Ability to apply knowledge of scientific theory and computer capability to design and recommend changes to methods for clinical research.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

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