Employment Opportunities

Employment Opportunities at Promedica International

We look for individuals with the following credentials. The following listings show the types of opportunities we have from time to time:

Project Manager
This position functions as the primary client interface for assigned projects, and is responsible for project staff procurement, training and management and adherence to established project schedule and budget. In addition to interacting with clients, this position may interface with clinicians, allied healthcare personnel, vendors, and FDA inspectors. Travel may be required.

General requirements are:

  • Established project management skills
  • Proficiency with Microsoft Word®, Excel® & Project® software
  • Thorough understanding of FDA regulations regarding conduct of clinical studies
  • Previous clinical trial management experience
  • BS or BA Degree and 7 years minimum related experience
Data Manager
This position functions as an interface with Project Management for assigned data management projects and is responsible for data management plans, requirements and database implementation schedules. Participates in the data system design, utilization, and maintenance for conformance with FDA guidelines and standard operating procedures. Reviews database implementation schedules, database utilization training, and database utilization efficiency. This position may interface with Project managers, Director IT, Systems Analyst, Statisticians, clinicians, clients, FDA inspectors. Travel may be required.

General requirements are:

  • Established data management skills.
  • Proficiency with SAS, Microsoft SQL, Word Excel, Access, Powerpoint and Outlook as well as web-based software system.
  • Thorough understanding of FDA regulations regarding management of data for clinical studies.
  • Previous data management, preferable CRO, experience.
  • Well-organized, strong attention to detail, good communication, documentation, follow-through and multi-tasking.
  • BS or BA Degree and 3 years minimum related experience.
In-House CRA
This position is based in PMI’s corporate office. Responsibilities include secondary EDC/CRF review, query management and some site management.

General requirements are:

  • Thorough understanding of GCP and FDA regulations related to clinical study conduct
  • Good knowledge of general medical terminology
  • Strong written and verbal communication skills
  • Organized, with good attention to detail, documentation and follow-through
  • Able to independently complete assigned activities
  • Proficiency with Microsoft Word® & Excel® software
  • BS or BA degree with 2 years minimum related experience
Regional CRA
(Mid-West, Eastern Seaboard or West Coast,Southern Calif)
This position is home or PMI based, and is responsible for clinical study monitoring activities within the defined region of the US. For assigned projects, the regional CRA is responsible for monitoring the implementation and regulatory compliance of study protocol activities and confirming data captured by assigned study sites. The position may require 50-75% travel. Organized home office systems are necessary for maintenance of study-related documentation.

General requirements are:

  • Thorough understanding of GCP and FDA regulations as they relate to clinical study conduct
  • Good knowledge of general medical terminology
  • Strong written and verbal communication skills
  • Organized, with good attention to detail, documentation and follow-through
  • Able to independently complete assigned activities
  • Proficiency with Microsoft Word® & Excel® software
  • BS or BA degree with 2 years minimum related experience

Please send your resume via regular mail, fax, or email to hres@promedica-intl.com:

Attn: Human Resources
Promedica International
3100 Bristol Street, Suite 250
Costa Mesa, CA 92626
Fax: 714.460.7364

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