Research Project Coordinator

University of MarylandBaltimore, MD
$48,000 - $53,000Hybrid

About The Position

The University of Maryland School of Medicine has two (2) exciting opportunities for full-time, regular Research Project Coordinators in the Marlene and Stewart Greenebaum Comprehensive Cancer Center (UMGCCC). These positions are responsible for coordinating the day-to-day operations of one or more research protocols. They serve as points of contact for study participants and office or clinical support personnel. Responsibilities include maintaining databases used to collect, analyze data, and track protocols and monitors and evaluates entries to maintain compliance with Federal and State regulations, policies, and procedures. The UMGCCC is a National Cancer Institute (NCI)-designated comprehensive cancer center which conducts innovative basic and clinical research that will impact the understanding and treatment of cancer around the world and seeks to provide state-of-the-art clinical care to cancer patients in Maryland and beyond. Private, foundation, and government sponsors provide funding to the Cancer Center to provide medical research treatment to cancer patients.

Requirements

  • Bachelor's degree in nursing, emergency services, chemistry, biology, public health, psychology or another scientific discipline appropriate to position required.
  • Prior experience in research, e.g., clinical research setting preferred.
  • Knowledge of position requirements.
  • Knowledge of all applicable requirements, regulations, and laws.
  • Skill in effective use of applicable technology/systems.
  • Ability to effectively communicate both verbal and written thoughts, ideas, and facts.
  • Ability to work cooperatively with others and independently.
  • Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Respect and Integrity, Well-being and Sustainability, Equity and Justice, and Innovation and Discovery.

Nice To Haves

  • Prior experience in research, e.g., clinical research setting

Responsibilities

  • Coordinating the day-to-day operations of research studies in the department such as data maintenance, grant expenditure adherence, project evaluation, meeting scheduling, and research subject interfacing.
  • Adhering to good clinical practices, study protocols, and applicable regulations.
  • Independently coordinating and communicating directly with the Principle Investigator, study participants, and sponsors to manage the operation and evaluation activities of the research studies.
  • Ensuring optimum efficiency and compliance with appropriate policies, procedures, and specifications.
  • Using evaluation techniques, originality, and ingenuity to resolve non routine issues.
  • Serving as a point of contact for study participants, research personnel and support staff.
  • Screening subjects for research studies by reviewing and obtaining source documents for potential participants.
  • Developing recruitment streams and advising participants of study objective, requirements, risks, benefits and obtaining their consent and enrollment.
  • Collecting baseline and follow-up data from subjects including verification of eligibility.
  • Obtaining demographic information.
  • Assessing for adverse events, obtaining concomitant medications, and interviewing subjects for follow-up.
  • Making recommendations concerning time-saving methods in data collection.
  • Coding adverse events in accordance with National Cancer Institute (NCI) common toxicity criteria.
  • Checking validity and accuracy of data ensuring compliance with quality control requirements.
  • Generating standard computer reports on patient demographics, and other pertinent data as requested.
  • Preparing reports on specific patient populations for investigators requesting data for research papers.
  • Monitoring activities to ensure compliance with protocols and all relevant local, federal, and state regulatory and institutional policies.
  • Assisting in budget development, expenditure adherence, and maintenance of inventory on equipment and supplies.
  • Determining reliability of data sources by evaluating information, determining errors and notifying responsible parties.
  • Performing other duties as assigned.

Benefits

  • Retirement program (pension or optional retirement plan/ORP)
  • Generous PAID leave package
  • Over 4 weeks of vacation accrued each year
  • 16 paid holidays
  • 3 personal leave days
  • Unlimited accrual of sick time
  • Comprehensive health insurance
  • Professional learning and development programs
  • Tuition remission for employees and their dependents at any University System of Maryland school
  • Flexible work schedules
  • Teleworking options (if applicable per job)
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