ClinicalPractices (GCP), and relevant regulations for the conduct of clinicaltrials including Title 21 Code of Federal Regulations (CFR), International Conference of Harmonization (ICH) and Good...
trials experience within a ClinicalResearch Site, CRO or eClinical service provider in a project management role or other equivalent experience 2+ years project management experience required working...
Piper Companies is currently seeking a Project Manager based in Philadelphia, Pennsylvania or open to occasional travel for work at a leading consumer health company. The Project Manager will...
Assist with InstitutionalReviewBoard (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations....
Job Details ClinicalResearch Coordinator/Data Manager Job Description Works under limited supervision and oversees the day-to-day activities of a clinicaltrial in accordance with Good ClinicalResearch...
/research coordination experience RequiredAt least three (3) years of clinical/research coordination experience Preferred Skills and AbilitiesBasic knowledge of IRB and human subject protectionExcellent...
Prepare and submit InstitutionalReviewBoard (IRB) applications and amendments. Ensure adherence to GoodClinicalPractice (GCP) guidelines, FDA regulations, and local regulatory requirements....
Job Description POSITION SUMMARY: We have an exciting opportunity for a leader with a clinicaltrial background to help stand up a lab in collaboration with our client....
Assist with InstitutionalReviewBoard (IRB) filings and inquiries, and assist in the preparation of manuscripts, grant proposals, and research related presentations....
Prepare and process all InstitutionalReviewBoard (IRB) submissions through the IRB and other regulatory groups as appropriate, including initial submissions, amendments, continuing reviews, adverse...
Independently manage different phases of clinicaltrials. They may assist with InstitutionalReviewBoard (IRB) filings, sponsor and investigator filings and research related presentations....
Prepare and process all InstitutionalReviewBoard (IRB) submissions through the IRB and other regulatory groups as appropriate, including initial submissions, amendments, continuing reviews, adverse...
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Clinical Trial Manager Online Courses and Training Opportunities
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This four-week clinical trials course is designed to create awareness about the availability and use of digital tools for the recruitment and retention of participants within clinical trials....
Whatever your role in clinical research, this online course from the University of Birmingham will build your statistical knowledge and skills directly applicable to clinical trials. In just three...
This course seeks to fulfill the clinical communitys need to improve skills in the critical evaluation of clinical research papers. Competency in critical appraisal skills can have a significant...
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