Research Project Manager - Rollins School of Public Health

Emory University•Atlanta, GA

3d•Hybrid

About The Position

This position supports a clinical research study funded by the National Institute of Environmental Health Sciences (NIEHS) Superfund Research Program (SRP). The prospective study examines relationships between chemical exposures and health outcomes in adults residing in Glynn County, Georgia. The Research Project Manager will play a central role in the day-to-day operations of the cohort and will work as an integrated member of a multidisciplinary research team that includes exposure scientists, epidemiologists, community engagement specialists, and community partners. The role requires an exceptional level or organization and willingness to work independently and proactively.

Requirements

A master's degree in public health, epidemiology, biostatistics, sociology, and psychology or related discipline and two years of professional level research experience, OR an equivalent combination of experience, education, and training.
Excellent oral and written communication skills.

Nice To Haves

Experience working with epidemiology or environmental health research and/or community-engaged research is strongly preferred.
Familiarity with biospecimen handling, exposure data management, or epidemiological cohort methods is a plus.
Candidates with existing relationships with communities in the Glynn County, Georgia area are encouraged to apply.

Responsibilities

Responsible for managing complex research projects.
Using an advanced knowledge of research methodology and techniques, assists in the planning and development of survey instruments, guidelines and procedures to collect required data.
Coordinates various aspects of the study.
Drafts and may edit text for studies.
Analyzes data, identifies data discrepancies and researches and identifies causes.
May perform statistical analysis of numerical data.
Actively contributes to the development of research protocols.
Determines how research methodologies or tools must be modified.
Ensures that study data and systems are maintained and accurately documented.
Analyzes data and develops reports to assess or monitor study performance and treatment results; may develop associated operational and statistical reports for management and regulatory agencies.
May oversee regulatory compliance efforts.
May develop and submit grant proposals and advise principal investigator of changes in reporting or accounting requirements.
May monitor expenses and receipts for active protocols.
Coordinates and conducts special meetings and presentations.
Coordinates computer support for ancillary studies conducted at off-site locations.
Collaborates on reports and papers.
Assists in the preparation of tables and graphs for publication and presentation.
May design and develop databases related to specific programs at the request of supervisor and/or Principal Investigator.
Performs related responsibilities as required.
Coordinating and supporting study visits with research participants, including participant scheduling, informed consent processes, biological specimen collection logistics, and data quality monitoring across longitudinal time points.
Conducting regular travel to Glynn County, Georgia to support field operations, maintain relationships with community partners, and ensure smooth execution of study protocols at local clinical and community sites.
Managing data related to questionnaires and biomarkers; responsibilities include data cleaning, tracking, documentation, and coordination with laboratory partners.
Serving as a liaison between the research team at Emory and community stakeholders in Glynn County, supporting ongoing community engagement efforts and helping ensure that the study is conducted in a culturally responsive and community-centered manner.
Coordinating across projects within the larger research center to ensure alignment of protocols and shared data needs.
Assisting with IRB submissions and amendments, protocol documentation, and regulatory compliance activities specific to human subjects research.
Supervising and mentoring study staff, including the on-site Clinical Research Coordinator, to ensure consistent protocol implementation and professional development.
Tracking study expenditures and coordinating with grants administration to monitor budget against project milestones.
Preparing and coordinating progress reports and other required communications to the NIEHS and SRP program officers.
Developing and maintaining standard operating procedures (SOPs) for study protocols, data collection, and biospecimen handling across longitudinal time points.
Developing and implementing participant recruitment and retention strategies to meet enrollment targets and support long-term cohort follow-up.