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Now actively recruiting for the following positions

Clinical Programmer

The Clinical Programmer works closely with Data Managers to build and maintain Electronic Data Capture system(s) and related custom reports.  Medidata Rave experience is required. This position may be office based in Durham, NC or home-based anywhere in the US.

 

Contracts Specialist

The Contracts Specialist is responsible for managing contracts from creation to completion including analysis of contract templates; creating and maintaining files for each contract; prioritizing daily activities according to importance and urgency; adhering to department turnaround times; and managing the approval and signature process for each type of contract.  This position will be office based in Durham, NC.

 

Clinical Trial Manager

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.

 

Project Manager

The Project Manager is responsible for managing all aspects of successful planning, implementation and execution of clinical trials including: timelines, budgets, quality, risks and overall cross-functional leadership in compliance with ICH-GCP, regulatory authority regulations and applicable Aperio SOPs.  The Project Manager serves as the primary client contact and is responsible for building and maintaining productive relationships.  The Project Manager serves as a functional line manager and does not have direct reports.  Oncology experienced is highly preferred.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

Clinical Support Specialist

The Clinical Support Specialist is responsible for the quality, regulatory compliance, and filing of site essential documents in the Trial Master File (TMF) during start-up and the maintenance phases of the study. The Clinical Support Specialist will ensure that documents maintained for a study comply with International Congress on Harmonization-Good Clinical Practices (ICH-GCP), country regulatory requirements, and procedures set forth by Aperio and its sponsors.  The Clinical Support Specialist works with both internal and external teams to ensure good communication to maintain study goals and may provide cross-functional assistance to support study and organizational goals.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

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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