in research studies or clinical trials to ensure compliance with protocols and meet clinical objectives.
Plan, develop, administer, and coordinate new or revised
project goals, objectives, work flows and policies through the
duration of the research study or clinical trial. Implement
approved study or trial policies and procedures.
Assist Principal Investigators and regulatory staff in the
preparation of new protocol submissions, protocol amendments, and
renewals of ongoing research studies or clinical trials. Support
and conduct data science activities across the IMPROVE 12 Maternal
Health Centers of Excellence in the U.S.
Ensure that goals and objectives specified for the research
project are accomplished in accordance within priorities, time and
funding limitations, or other specifications.
Evaluate project effectiveness in order to develop and
implement new or improved methods. Devise and implement evaluation
methodologies.
Oversee subject enrollment to ensure that informed consent is
properly secured and documented. Assess eligibility of potential
subjects through methods such as screening interviews, reviews of
medical records, and discussions with research personnel. Oversee
the development and dissemination of internal and external Data Hub
communications (eg., meetings, reports, newsletters,
webinars).
Coordinate research project activities through delegation of
assignments to staff.
Monitor activities to ensure compliance with protocols and all
relevant local, federal, and state regulatory and institutional
policies. Continuously educates and trains personnel on compliance
and protocol. Identify protocol problems, informs investigators,
and assist in problem resolution efforts.
Manage complex study or trial data. Develop methods for
collection, database storage, tracking, analysis, and
interpretation of data.
Develop and prepare project or research related documentation
such as protocol worksheets, procedural manuals, adverse event
reports, case report forms, and institutional review board
documents. Responsible for developing and producing custom and
routine reports.
Coordinate budget development, expenditure adherence, grant
applications, and maintenance of inventory on equipment and
supplies.
Recommend additional equipment and resources for the program.
Review proposed study protocols to evaluate factors such as sample
collection process, data management plans, and potential subject
risks. Conducts quality assurance audits on data and regulatory
documentation.
Provide training and guidance to less experienced
personnel.
Attend research study or clinical trial related meetings,
conferences and teleconferences, as well as participating in any
additional planning and development related activities.
Perform other related duties as assigned.
Qualifications :
MINIMUM QUALIFICATIONS
Education: Bachelor's degree in nursing, emergency services,
chemistry, biology, public health, psychology or another scientific
discipline appropriate to position required. Preferred applicants
with advance graduate degrees in public health, epidemiology,
maternal health, public administration, or public
administration.
Experience: Three (3) years of research coordination
experience with at least two (2) years in research specialization.
Experience working in a public health setting or conducting public
health research is preferred.
Other: Except for qualifications established by law,
additional related experience and formal education in which one has
gained the knowledge, skills, and abilities required for full
performance of the work of the job class may be substituted for the
education or experience requirement on a year-for-year basis with
30 undergraduate college credits being equivalent to one year of
related experience. In instances where specific education and/or
experience is required only directly related education and/or
experience may be substituted.
KNOWLEDGE, SKILLS, ABILITIES
- Knowledge of position requirements, related regulations and
laws.
- Skill in effective use of applicable technology/systems.
- Able to exercise initiative and resourcefulness to prioritize
multiple ongoing and competing projects.
- Ability to effectively communicate both verbal and written
thoughts, ideas, and facts.
- Ability to work cooperatively with others and
independently.
- Ability to accept feedback gracefully, be personable and
maintain a professional attitude.
Hiring range : $70,500.00 - $80,000, Commensurate with
education and experience
UMB is committed to cultivating a diverse and inclusive workforce
and is proud to be an equal employment opportunity employer. All
qualified applicants will receive consideration for employment
without regard to race, color, religion, age, ancestry or national
origin, sex, pregnancy or related conditions, sexual orientation,
gender identity or expression, genetic information, physical or
mental disability, marital status, protected veteran's status, or
any other legally protected classification.
If you anticipate needing a reasonable accommodation for a
disability under the Americans With Disabilities Act (ADA), during
any part of the employment process, please submit a
UMB Job Applicant Accommodation Request . You may also contact
leave_and_accom@umaryland.edu
. Please note that only inquiries concerning an ADA request for
reasonable accommodation will be responded to from this email
address.
The University of Maryland, Baltimore prohibits sex discrimination
in any education program or activity that it operates. Individuals
may report concerns or questions to the Title IX Coordinator. Read
the
UMB Notice of Non-Discrimination for more information.