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Now actively recruiting for the following positions

Senior Clinical Programmer

The Senior Clinical Programmer is responsible for programming and testing Electronic Data Capture system(s), data listings, and reports utilizing specialized software that supports data collection, cleaning and analysis for conducting clinical trials.  This is a customer facing role.  Medidata Rave experience is required. This position may be office based in Durham, NC or home-based anywhere in the US.

 

Clinical Trial Manager (CTM)

The Clinical Trial Manager is a Clinical Trial Management expert focused on the execution of clinical trials and brings that expertise to the design and conduct of clinical studies in alignment with Aperio’s corporate strategy. Responsible for operational leadership and expertise in the planning, implementation, and management of clinical studies through all periods of study conduct. In conjunction with the cross-functional project team, the Clinical Trial Manager is responsible for operational aspects of assigned clinical studies to ensure successful completion of projects on time, within budget, and in compliance with SOPs, Regulatory Authorities, ICH/GCP guidelines and ensure delivery of company goals.  Oncology experience is highly preferred.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

Associate Technology & Analytics Programmer

The Associate Technology & Analytics Programmer is responsible for providing programming support for data management, study monitoring, and company metrics.  The Associate Technology & Analytics Programmer will assist in developing programs to build study tools and monitor the quality of the data collected as well as to generate reports to inform the progress of the studies and to summarize the study data from a scientific and operational perspective.  This position will be office based in Durham, NC.

 

Aperio Clinical Outcomes provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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

Offering both full and part-time positions, we match clinical research 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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