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Criterion Edge is hiring a Junior Regulatory Consultant to provide hands-on support for established regulatory processes. The role focuses on standards management, documentation updates, submission preparation, compliance records, and regulatory research and coordination. Responsibilities Support ongoing standards management activities, including monitoring, tracking, and maintaining applicable regulatory and consens

Responsibilities Design, execute, and interpret experiments on antigen expression, purification, characterization, adjuvant selection, and formulation (independence increases with level) Perform core molecular biology, microbiology, and cell culture techniques (PCR, cloning, Western blot, ELISA) Run and, at senior levels, develop immunological assays (SNT, VN, HI, ELISA, ELISpot, multiplex cytokine, FACS) Support or

Parexel is actively hiring multiple Clinical Research Associates and Senior Clinical Research Associates to join their growing team. The CRA is responsible for the delivery of studies at allocated sites, ensuring compliance with international guidelines and local regulations while managing site performance and study conduct. Responsibilities Contributes to the selection of potential investigators In some countries, a

Responsibilities Act as the main line of communication between the project team, sponsor, and the site Build and maintain a good relationship with the site staff involved in the study conduct Prepare, conduct, and report site selection, initiation, routine monitoring and close-out visits Ensure that subject recruitment targets are timely defined, communicated, recorded and met, and project timelines are followed at s

Clinical Project Manager I/Clinical Project Manager II/Senior Clinical Project Manager Tags 81 GOOD MATCH Experience Level 100 Skill 76 Industry Exp. 75 Clinical Trials Pharmaceutical Biotechnology Healthcare Responsibilities Lead planning and execution of clinical trial projects from proposal through closeout Act as primary sponsor liaison, ensuring alignment on scope, timelines, and deliverables Develop and maintai

Penn State University is hiring a full-time Clinical Research Coordinator to support the INSPIRE team within the Department of Pediatrics, Division of Hematology and Oncology. The role oversees pediatric oncology research projects, including participant recruitment, data collection and management, regulatory and IRB compliance, project coordination, documentation, and collaboration with investigators and stakeholders

Parexel is seeking a Clinical Research Associate to serve as the primary site contact and site manager throughout all phases of clinical research studies. The role manages site relationships, monitoring activities, regulatory documentation, compliance, and collaboration with investigators and study teams across multiple protocols and therapy areas. Responsibilities Act as the primary site contact and site manager thr

ICON Strategic Solutions is a sponsor-dedicated clinical research organization that provides global expertise and supports the development of treatments benefiting patients worldwide. The Clinical Research Associate will conduct and monitor clinical trials in multiple therapeutic areas, including oncology, while ensuring protocol compliance, data integrity, and patient safety. The role also involves collaborating wit

Responsibilities Conducting laboratory, field, or computational research activities Collecting, managing, and analyzing research data Assisting with experimental design and protocol implementation Maintaining laboratory equipment, materials, and documentation Contributing to manuscripts, reports, and presentations Collaborating with faculty, staff, graduate students, and other research personnel Preferred Ability to