Post Doctoral.Post Doctoral.Associate

University of Pittsburgh • Pittsburgh, PA

3d

About The Position

Lead and contribute to data analysis across the CREATE clinical dataset, including biopsychosocial phenotyping and quantitative sensory testing (QST), while coordinating scientific activities across the five-site consortium, including data harmonization, protocol fidelity, and cross-site working groups. Prepare first-author and co-author manuscripts for peer-reviewed publication and contribute to grant development, including aims, preliminary data, and analytic plans for follow-on funding. Support patient engagement activities and participate in consortium-wide governance and steering committee meetings. Mentor graduate and undergraduate trainees within the research team and present findings at national and international scientific meetings (e.g., USASP, IASP, AAPM).

Requirements

• PhD, MD, or equivalent doctoral degree in neuroscience, clinical psychology, biostatistics, public health, rehabilitation science, or a related field.
• Strong quantitative skills.
• Experience with R, Python, MATLAB, or comparable platforms.
• Demonstrated record of peer-reviewed publication appropriate to career stage.
• Excellent written and oral communication skills.
• Ability to work effectively in a collaborative, multi-site team environment.

Nice To Haves

• Experience with chronic pain research, TMD, or musculoskeletal/orofacial pain populations.
• Familiarity with QST methodology and biopsychosocial assessment frameworks.
• Background in multi-site clinical trial coordination.
• Experience with IRB processes.
• Experience with Common Data Elements (NIH HEAL / NIDCR).
• Track record of patient engagement or community-engaged research.

Responsibilities

• Lead and contribute to data analysis across the CREATE clinical dataset, including biopsychosocial phenotyping and quantitative sensory testing (QST).
• Coordinate scientific activities across the five-site consortium, including data harmonization, protocol fidelity, and cross-site working groups.
• Prepare first-author and co-author manuscripts for peer-reviewed publication.
• Contribute to grant development, including aims, preliminary data, and analytic plans for follow-on funding.
• Support patient engagement activities.
• Participate in consortium-wide governance and steering committee meetings.
• Mentor graduate and undergraduate trainees within the research team.
• Present findings at national and international scientific meetings (e.g., USASP, IASP, AAPM).

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Ph.D. or professional degree