PRA (Pharmaceutical Research Associates) Health Sciences provides clinical development services. Some of its services include drug development and regulatory strategy plans, phase I clinical trials, phase II through IV multi-center clinical trials, development and analysis of integrated global clinical databases, and preparation and submission of regulatory filings in North America and Europe. PRA has more than 11,000 employees operating in 80 countries, and has the following career openings at its Blue Bell location:

Operations Program Specialist

This position will assist in the creation of and maintenance of project management, program management, and or functional operational management templates, documents, tracking tools, and databases. He/she will run reports from PRAHS or client systems as needed to compile, provide first level review, and monitor performance metrics. The person will support collection and monitoring of project and/or program performance utilizing metrics data, and support collection and presentation of information for routine project and/or program review, functional operational review, and quarterly executive review.

The ideal candidate will possess a Bachelor’s Degree, and have at least three years of experience in clinical research in a similar position. He/she must have Pharma and/or CRO experience. The person must also have the ability to create complex Excel workbooks and utilize pivot tables and macros.

Click here to read more about the Operations Program Specialist position at PRA Health Sciences.

Senior Global Data Manager

This position takes a leadership role with the CRO, the trial customer(s), and other internal and external partners to establish, align, and confirm data management expectations for assigned trial(s). He/she gathers content and integration requirements for eCRF and other data collection tools. The person establishes conventions and quality expectations for clinical data, and establishes expectations for dataset content and structure. This position will also set timelines and follow-up regularly to ensure delivery of all Data Management milestones.

The ideal candidate will possess a Bachelor’s Degree, and have data management experience. He/she should have experience in clinical drug development within the pharmaceutical industry or related industry. Vendor oversight experience and team leadership experience is also required.

Click here to read more about the Senior Global Data Manager position at PRA Health Sciences.

Site Management Associate 2

This position performs investigative site recruitment/feasibility, essential document collection and review, clinical status tracking, in-house site management, and data review activities in accordance with the study protocol. He/she ensures sponsor and investigator obligations are met in compliance with applicable guidelines and local regulatory requirements. The person will also participate in sponsor and project-related meetings and appropriately interact with client and team.

The ideal candidate will possess a Bachelor’s Degree in a clinical, science, or health-related field. Prior experience using computerized information systems is required, as is at least one year of experience with clinical trials support, Data Coordination, or in the pharmaceutical industry.

Click here to read more about the Site Management Associate 2 position at PRA Health Sciences.