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ICON plc
Overview
The Informed Consent Writer is responsible for creating health-literate informed consent documents for clinical trials across various therapeutic areas. This includes collaborating with protocol authors and managing the design and planning of documentation to ensure timely delivery and regulatory compliance.
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Compensation
Salary not listed
Posted
22 days ago
Arrowhead Pharmaceuticals
Provide clinical pharmacology and pharmacometrics leadership for assigned development programs, contributing to clinical trial design and performing hands-on PK/PD analyses. Oversee the preparation of PK analysis reports and clinical pharmacology components of global regulatory submissions.
$120,000 - $170,000 / YEAR
1 month ago
Premier Health
The Research Nurse provides expertise in reviewing and implementing clinical trials for eligible patients, which includes assessing eligibility, conferring with physicians, and educating patients and families. This role ensures treatment implementation aligns with the clinical trial design while performing quality data collection for research groups.
2 months ago
City of Hope
This role involves comprehensive project management, scientific writing, and clinical protocol development for the Thoracic Oncology Program, guiding projects from initial conception through grant submission, clinical execution, and final manuscript preparation. Responsibilities include supporting project design, managing grant logistics, coordinating regulatory applications (IRB/IACUC), and ensuring clarity in data presentations and publications.
3 months ago
