Clinical Trials Jobs in Cincinnati, OH

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

The Lead Data Manager is responsible for all data management activities in assigned clinical trials under supervision.Acts as primary communication point for project teams and company departments regarding clinical data managementActs as primary communication point for clients/vendors More...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

Position: Data Entry Clerk Work From Home PartTime Focus Group Participants (Side Gig)We are seeking individuals to participate in National & Local Paid Focus Groups Clinical Trials Phone Interviews or Paid Surveys.With most of our paid surveys you have the option to participate remo More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

Industry: HealthcareClinical Nurse Specialist CVICULocation: Santa Clara CAResponsibilities:Clinical Expertise: Provide expert consultation and guidance to nurses and other healthcare providers in the CVICU.Education & Mentorship: Develop and implement educational programs for nu More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...

Provides indepth clinical expertise in a defined area of nursing practice (eg. pediatrics oncology adult medicine). Develops and ensures quality standards for nursing practice for a specific patient population. Provides advanced clinical practice education consultation research and ad More...

Korzen Health is working with one of the fastest growing wound care treatment companies in the nation. We are looking to hire a Clinical Specialist that will work within our team of providers. We specialize in the biological treatment and management of chronic wounds. The patented 3C More...

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications maintaining the highest quality standards in the industry.You will:Act as the main line of communication between the project team spon More...