Join Our Team

Now actively recruiting for the following positions

EDC Clinical Programmer
Seeking an EDC programmer with C# and/or VB Script experience. Medidata experience is a plus.
Core duties include: Managing EDC programming tasks including eCRFs, edit checks, custom functions, system/core configuration, rights and roles, and report development as required by project scope of work and Data Management Plan. The ideal candidate has experience: collaborating with clinical team (DMs, CRAs, Safety, Bios, etc.), liaising with internal, sponsor, and vendor team members, experience using Visual Basic/VB Script, SQL, HTML, and XML, and the ability to create detailed programming instructions and documents (technical guides, working practices, templates). This is a full-time, permanent role. This position may be office-based in Morrisville, NC or home-based in the U.S.

We’re always expanding our global network of qualified
clinical professionals.

Offering both full and part-time positions, we match clinical professionals with job opportunities, whether you are an independent contractor or prefer employee status.

We are always accepting resumes for the following roles in North America, Europe, and other targeted areas:

  • Senior CRA (Clinical Research Associate)
  • Senior Project Manager (PM)
  • CTM (Clinical Trial Manager)
  • Clinical Support Specialist
  • Proposal Analyst
  • Director, Business Development
  • Lead Clinical Data Manager
  • Clinical Data Specialist
  • Safety Specialist
  • Medical Writer
  • Medical Monitor
  • EDC Programmer

Current Job Openings


Contract CRA

INNO Clinical is always looking for experienced, regionally-based contract CRA’s to support our clinical projects.

RESPONSIBILITIES

  • Monitor Phase I-IV clinical studies in all types of therapeutic areas.

REQUIREMENTS

  • Minimum 7 years of monitoring experience preferably with at least 3 years as an independent contractor.
  • Ability to travel as needed.

Submit Your Resume


Project Manager/Sr. Project Manager – Full-Time

INNO is seeking an experienced Project Manager in our Morrisville office to manage the execution of small to large global clinical studies from initiation through close-out. This is a fast paced position working with a strong, collaborative team of professionals.

RESPONSIBILITIES

  • Serve as the primary interface with client representatives as well as vendors and INNO personnel to ensure the timely initiation and completion of clinical trials.
  • Lead problem solving and resolution efforts to include management of risk, contingencies and issues.
  • Manage and coordinate efforts of cross-functional project teams to support milestone achievements.
    • Manage budgets and contracts throughout the duration of the study.

REQUIREMENTS

  • Minimum 5  years clinical project management experience preferably with global clinical projects.
  • Prefer strong CNS study experience.
  • Excellent customer service and presentation skills.
  • Computer proficient.
  • Ability to manage competing priorities.
  • Working knowledge of GCP’s, ICH guidelines and FDA regulations.

Submit Your Resume


Submit Your Resume

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