Join Our Team

Now actively recruiting for the following positions

 

Clinical Programmer (Senior or Principal)

The Clinical Programmer is responsible for all aspects of programming and testing Electronic Data Capture system(s).  This role is very interactive therefore must be experienced in conducting on-line screen review meetings or other discussions.  In addition to EDC development, the clinical programmer will also play a key role in development of data listings and reports utilizing specialized software that supports data cleaning for analysis of clinical trial data.   Medidata Rave experience is strongly preferred, certification a plus.  This position may be office based in Durham, NC or home-based anywhere in the US.

 

Clinical Data Specialist

The Clinical Data Specialist is responsible for providing a complete and clean database per industry standards and client specifications.  The Clinical Data Specialist 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.

 

Senior Safety Specialist – Device

The Senior Safety Specialist is responsible for processing adverse event information and ensuring Safety department activities are completed in accordance with all relevant regulations and guidelines.  Primary responsibilities include:  serving as the Safety Lead on device studies; processing and reporting incoming safety events; authoring adverse event narratives; query generation; reporting to regulatory authorities as required.  Must possess prior Safety experience supporting device studies. Preference for a professional from a health-related field.  This position may be office based in Durham, NC or home-based anywhere in the US.

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

Section

First Name
Last Name
Email Address
Position applying for:
Name of Referral
Name of Conference/Tradeshow
Comments

Section

Maximum upload size: 268.44MB