- AbbVie (North Chicago, IL)
- …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other ... reputation as an industry leader. + Responsible for having deep understanding the regulatory requirements related to the clinical studies and global drug… more
- AbbVie (North Chicago, IL)
- …are innovative and aligned with regional demands. + Ensure compliance with regulatory requirements and global standards in clinical development. This requires ... to direct reports, enhancing team capabilities and performance. + Engage with regulatory bodies and strategic partners to advance clinical development… more
- AbbVie (North Chicago, IL)
- …interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study reports, regulatory submissions and responses, and other ... May represent AbbVie at key external meetings. + Responsible for understanding the regulatory requirements related to the clinical studies and global drug… more
- Rush University Medical Center (Chicago, IL)
- …of each case. **Summary:** The position supports the Office of Research Affairs ' Clinical Research Administration Division, their clinical department ... are conducted in accordance with the principles of Good Clinical Practice (GCP) .S/he will coordinate and manage multiple...a timely manner. * Submits or partners with a regulatory coordinator to submit study related documents, study protocols… more
- Abbott (Abbott Park, IL)
- …limited supervision. Applies subject matter knowledge in the area of Medical Affairs . Requires capacity to apply skills/knowledge within the context of specific ... needs or requirements. + As the Experienced professional in the Medical Affairs Sub-Function, possesses well developed skills in overseeing the direction, planning,… more
- AbbVie (North Chicago, IL)
- …programs under consideration. + Reviews and provides clinical operations content to clinical and regulatory documents (eg, INDs, IB, NDAs, BLAs, MAA, ... YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Clinical Operations Program Director is responsible to connect science and… more
- Rush University Medical Center (Chicago, IL)
- …to accommodate study and patient schedules. * Demonstrated knowledge of clinical research principles, regulatory requirements, and ethical guidelines required. ... Offers may vary depending on the circumstances of each case. **Summary:** The Clinical Research Nurse Manager is a professional registered nurse who is responsible… more
- Rush University Medical Center (Chicago, IL)
- …to clinical research with probationary period. * Ability to communicate complex clinical and regulatory concepts in layperson language. * Ability to build ... who, as part of a research team, will provide clinical care within the context of a clinical...PI, sponsor, medical monitor, compliance, staff, Office of Research Affairs and manager to identify and improve routine processes… more
- Abbott (Abbott Park, IL)
- …products for treatment of vascular disease. As the Specialist in Global Clinical Affairs , considered as highly experienced and knowledgeable resource within ... colleagues serve people in more than 160 countries. **Job Title** **Principal Field Clinical Specialist** **Working at Abbott** At Abbott, you can do work that… more
- Sumitomo Pharma (Springfield, IL)
- …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. **Job ... as required. + Coordinate responses to ad hoc safety issues such as regulatory authority, site, or health care professional requests, along with PV physician,… more
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