Entry Clinical Trials Feasibility Specialist
Cincinnati, Ohio
Entry Clinical Trials Feasibility Specialist Job Locations United States-OH-Cincinnati Category Feasibility & Proposals Job Summary We are currently seeking an Entry Feasibility Coordinator, who will be a member of our global clinical opera...
22d
| Job Type | Full Time |
Cincinnati, Ohio
Feasibility Manager Job Locations United States-OH-Cincinnati Category Feasibility & Proposals Job Summary We are currently seeking a Feasibility Manager, who will be a member of our global clinical operations team. By working cross functio...
22d
| Job Type | Full Time |
CRA/CRC to Site Relationship Coordinator
Cincinnati, Ohio
CRA/CRC to Site Relationship Coordinator Job Locations United States-OH-Cincinnati Category Clinical Research Associate Job Summary The Site Relationship Coordinator is a new role within the Clinical Monitoring team at Medpace that offers t...
22d
| Job Type | Full Time |
Clinical Research Associate (Physical Therapist Candidates)
Cincinnati, Ohio
Clinical Research Associate (Physical Therapist Candidates) Job Locations United States-OH-Cincinnati Category Clinical Research Associate Job Summary We are hiring Physical Therapists at Medpace! The Clinical Research Associate position at...
22d
| Job Type | Full Time |
Fairfield, New Jersey
Consumer Product Testing Company
Job Type: Part Time. Monday through Friday, Flexible Hours 25 Hours per Week MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and expe...
22d
| Job Type | Part Time |
Fairfield, New Jersey
Consumer Product Testing Company
Job Type: Full Time. Base Hours: 9:30AM - 6:30PM Monday through Friday MINIMUM QUALIFICATION REQUIREMENTS To perform this job, an individual must be able to perform each essential duty satisfactorily, and meet the educational and experience...
22d
| Job Type | Full Time |
Cambridge, Massachusetts
The Principal Medical Writer represents medical writing on multi-disciplinary teams, collaborates on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Proced...
22d
| Job Type | Full Time |
Associate Director, Biostatistics
Cambridge, Massachusetts
The Associate Director, Biostatisticsis responsible for statistical activities in support ofclinical trials, including contributing to trial designs, authoring statistical sections of protocols,preparing statistical analysis plans, and revi...
22d
| Job Type | Full Time |
Associate Director, Case Management Vendor Oversight
Cambridge, Massachusetts
This role is considered Hybrid. Overview This position develops, implements, and oversees processes and procedures for clinical trial ICSR processing activities, including oversight of the case processing outsourced service provider(s). The...
22d
| Job Type | Full Time |
Cambridge, Massachusetts
Responsibilities: Responsible for all aspects of clinical study planning and execution within pre-specified clinical development program, timelines and budget and includes, but is not limited to, preparation of study related materials, rela...
22d
| Job Type | Full Time |