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Now actively recruiting for the following positions

Lead Clinical Data Manager

The Lead Clinical Data Manager (LCDM) is responsible to manage all data management tasks from project start-up to database lock, and to produce a clean and analyzable database.  The LCDM serves as a technical leader and is the project and client liaison.  The LCDM provides management and provision of project specific data management status, cycle time, and productivity metrics.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

Clinical Data Specialist

The Clinical Data Specialist (CDS) is responsible for providing a complete and clean database per industry standards and client specifications.  The CDS will: issue queries and review query responses; support system development and validation; support the creation and maintenance of documentation for studies.  This is not a customer facing role.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

Manager, Clinical Study Support (CSS)

The Manager, CSS is responsible for the management and strategic leadership of clinical support services to include the planning, implementation and management of study start-up, maintenance, and closeout of project(s); ensures quality standards are maintained and Aperio SOPs and ICH GCP are followed across clinical research projects. This is a line management position and client facing. This position will be office based in Durham, NC, ideally coming into the office 1 – 2 times a week or as needed.

 

Clinical Trial Manager/Sr. Clinical Trial Manager

The Clinical Trial Manager (CTM)  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.

 

Medidata Rave Custom Function Programmer

The Custom Function 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.  Medidata Rave custom function programming (C#) experience is required. This position may be office based in Durham, NC or home-based anywhere in the US.

 

Medical Coder

The Medical Coder is responsible for providing medical coding and data management support to the study team and Lead Data Manager. The Medical Coder performs coding and other tasks as assigned from project start-up to database lock in order to produce a clean and analyzable database. 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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