Jobs with PRA International

Manages study procedures and operational activities of the Clinical Pharmacology Center (CPC) to ensure high quality client satisfaction and PRA profitability. ACCOUNTABILITIES Develops and manages

Due to our continued growth, we currently have a great opportunity for experienced Clinical Programmers (SAS). These positions can be located in our Raleigh, NC Lenexa, KS, or Horsham, PA offices. The

The Business Unit : Early Development Services PRA's Early Development Services (EDS) group, is one of the business units within PRA that provides comprehensive services such as Phase I and IIa clinic

Accountabilities: 1. Screens potential volunteers according to the protocol for each study. 2. Provides clinical care to volunteers in accordance with protocols including clinical assessment and foll

Conducts PK/PD analyses, interprets and reports results, and contributes to all phases of a clinical study involving PK/PD characterization. ACCOUNTABILITIES On the project level, assists in study

As a Clinical Data Coordinator joining our global team of more than 200 data management professionals, you will learn the basic principles of Data Management in Clinical Research. Performing a wide va

GENERAL SUMMARY Serves as principal investigator or sub-investigator for clinical studies conducted at the CPC. Manages the delivery of medical services to study subjects. ACCOUNTABILITIES Manages s

Manages clinical operations activities. Provides leadership in the implementation of PRA's quality initiatives and business processes, achievement of its management goals and objectives within the fra

The Business Unit : Early Development Services PRA's Early Development Services (EDS) group, is one of the business units within PRA that provides comprehensive services such as Phase I and IIa clinic

The Document Management Associate is responsible for: the preservation of original document integrity and security; the setup, maintenance, and delivery of the Trial Master File; the setup, maintenanc

Due to our continued growth, we currently have a great opportunity for experienced Clinical Programmers & These positions can be located in our Raleigh, NC, Lenexa, KS, or Horsham, PA offices. The c

Under close supervision, performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, and in-house site management activities to ensure thes

PRA International is hiring a Clinical Data Administrator in Lenexa, KS office. This is a dual role that combines the duties of a Clinical Data Processor with Client and Site Support tasks. Clinical D

The Document Management Associate is responsible for: the preservation of original document integrity and security; the setup, maintenance, and delivery of the Trial Master File; the setup, maintenanc

We currently have an excellent opportunity for a Project Director/ Senior Project Manager with a background leading clinical trials (Phase II and III) in Infectious Disease (HepB/ C). Neurology, Oncol

We currently have an excellent opportunity for a Project Director/ Senior Project Manager with a background leading clinical trials (Phase II and III) in Neurology, Oncology, Rheumatology, Immunology

PRA International is seeking an experienced Drug Safety Associate to manage individual case safety reports (SAEs, ADRs, AEs of special interest and other types), reconciliation of SAEs, coding and dat

Interprets regulations and guidance documents governing cGCP and applies the interpretation to daily work for the PRA staff and client representatives Researches the published information, i

We currently have an excellent opportunity for a Project Director/ Senior Project Manager with a background leading clinical trials (Phase II and III) Oncology, Rheumatology, Immunology, CNS or Infe