← Search all jobs

Clinical Research Specialist, Radiation Oncology

University Of Maryland Medical System

Baltimore, MD · Posted September 30, 2026

No experience needed. The posting says: “No experience is required.”

Just laid off? Start here: a plan for the first weeks

See every open role at University Of Maryland Medical System

More in Maryland job market · Healthcare & Hospital Systems · Clinical jobs

More roles at University Of Maryland Medical System

Where Baltimore, MD ranks

Where Baltimore, MD placed in our monthly rankings, month by month. Each month stays online at its own address.

Rankings about clinical jobs

Clinical jobs · Top Clinical employers · All rankings

How AI is used in this kind of work

AI use among medical scientists, except epidemiologists is little observed so far. Measured exposure for medical scientists, except epidemiologists: 4% (little observed).

Share of this job’s tasks that AI is already used for at work, from real usage. It is not a forecast of job loss, and a low number means no use seen yet. Source: Anthropic Economic Index.

Check how this applies to your own job

About the job

Job Requirements

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.

Principal Responsibilities and Tasks

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. N

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.

Represents department at research and protocol initiation meetings.

Work Experience

Education and Experience

1Bachelor’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.

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.

Ability to network with, and present information to key groups and individuals.

Ability to conduct library research and participate in the preparation of journal articles.

Ability to complete and administer complex research protocols.

Knowledge of best practice in Clinical Research.

Patient Safety

Ensures patient safety in the performance of job functions and through participation in hospital, department or unit patient safety initiatives.

Takes action to correct observed risks to patient safety.

Reports adverse events and near misses to appropriate management authority.

Identifies possible risks in processes, procedures, devices and communicates the same to those in charge.