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Investigator or Trial or FDA jobs in Columbus, OH, 43215

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Job alert Jobs 11 - 20 of 219

Medical Reviewer/Safety Reviewer - A

Experis  –  Columbus, OH, 43219
... with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and ... - May 04

Medical Safety Reviewer

DivIHN Integration Inc  –  Columbus, OH
... with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and ... - May 03

Research/Regulatory Nurse Practitioner - Gene Therapy

Nationwide Children's Hospital  –  Columbus, OH, 43215
... as directed by the Principal Investigator (PI), this position performs all research patient management activities, ... staff, assists in the writing of FDA Annual Reports, OBA reporting, preparation of DSMB reports, and Clinical Study Reports. ... - Apr 16

MSL Field Director, Immunology - Rheumatology (Northeast)

AbbVie  –  Columbus, OH
... Evaluate appropriate tools and analytics to ensure optimal trial performance through investigator engagement and excellence in collaboration and coordination with clinical operations within the geographic region. Regional Execution of Field-Medical ... - Apr 07

Medical Safety Reviewer

DivIHN Integration Inc  –  Columbus, OH, 43219
... with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and ... - May 04

Medical Safety Reviewer

DivIHN Integration Inc  –  Columbus, OH, 43219
... with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and ... - May 04

Medical Safety Reviewer

DivIHN Integration Inc  –  Columbus, OH, 43219
... with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... May provide training internally and at investigator meetings on safety issues, responsible for serious adverse events and ... - May 04

Scientific Writer Sr

Nationwide Children's Hospital  –  Columbus, OH
... CONNECT works alongside phase I consortia and large clinical trial groups to target high-risk pediatric and young adult ... written responses to queries from the IRB, scientific review committees, FDA, Data Safety Monitoring Committee etc. ... - Apr 27

Associate Director, Manufacturing (GMP)

Amplifybio, LLC  –  New Albany, OH, 43054
... GMP Compliance: Oversee all manufacturing activities to ensure compliance with GMP regulations, FDA guidelines, and industry ... Production Planning: Develop and execute production schedules to meet clinical trial and commercial supply requirements, ... - May 02

Associate Director, Manufacturing (GMP)

Amplifybio, LLC  –  New Albany, OH, 43054
... GMP Compliance: Oversee all manufacturing activities to ensure compliance with GMP regulations, FDA guidelines, and industry ... Production Planning: Develop and execute production schedules to meet clinical trial and commercial supply requirements, ... - May 02
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