670 data-"https:" "https:" "https:" "https:" "https:" "https:" "SciLifeLab" "IFM" "IFM" positions at University of Pennsylvania
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
for all aspects of study coordination including subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up and regulatory documentation. Job Description Job
-
enhances faculty support across divisions. The role drives operational excellence by integrating clinical research finance with departmental research administration, championing process redesign, data and
-
, participant recruitment and retention, data collection and management, coordination across interdisciplinary teams, and engagement with community and institutional partners. The role supports the efficient
-
manufacturing data:, and annual reporting to regulatory bodies, and any FDA requests for information. The Manager of the Regulatory and CMC unit is a supervisory role and will direct a team of 3-4 quality
-
benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Data Research
-
of Pennsylvania is a pioneering interdisciplinary research lab dedicated to applying computational methods and large-scale data to some of the most pressing challenges facing society. Founded and led by Duncan
-
for the Graduate Student Center first floor information desk and Family Center visitor desk. As the first point of contact for many visitors, the Administrative Coordinator sets the tone for a positive experience by
-
, collecting and reporting research data, accessing and reporting AE/SAEs per protocol, managing subject treatment per protocol, oversight and coordination of research testing, including labs, office visits and
-
deficiencies and design and implement changes to mitigate risks. Manage communication and information flow with departments and stakeholders; provide exceptional customer service by responding promptly
-
. Ensure study/trial data integrity and regulatory compliance with GCP guidelines, Federal/FDA regulations, and institutional/sponsor requirements. Supervise CRCs and CRNs as assigned. Supporting project