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Team Lead Clinical Operations

Raleigh
Permanent
Reference: JR071710
Description

Team Lead, Clinical Operations

The Role

Fantastic opportunity to join ICON and in particular Accellacare Site Networks as a Team Lead, Clinical Operations at ICON. This permanent opportunity, reports directly to the Clinical Operations Manager, with the primary aim of Coordinating clinical trials and/or providing coordinator support as directed by Manager. This position may involve travel between sites.

Our mission is to function as an Integrated Site Network, the role of our Team Leads are paramount to achieving our mission.

As a Team Lead, Clinical Operations you will be responsible for the following tasks:

* Assisting Site Manager with organizing, preparing for and conducting staff
meetings.
* Proactively overseeing recruitment needs and initiatives as needed.
* In the absence of the Manager, overseeing daily site activity.
* Independently managing projects and/or relationships at the direction of the Manager.
* Assisting with staff resource identification, development and utilization, ensuring optimal site performance.
* Serving as a marketing representative of the organization with regard to recruitment and retention of studies and development of contacts within the pharmaceutical industry.
* Advocates and contributes to the customer service performance of the sites to ensure optimal relationships with volunteers and industry clients.
* Promotes business growth through collaborating with Manager for trial feasibility completion, including but not limited to the assessment of trials, investigator and staff involvement and related correspondence with industry.
* Establishes and cultivates productive relationships with monitors and industry personnel to enhance business opportunities for the site and organization.
* Provide training and mentoring for the development of site personnel and investigators to facilitate the business development process.
* Oversee the process by which we obtain and include investigators in the clinical trial process, including investigator related documents (i.e., research agreement, malpractice coverage, W9, etc.) and internal communications to ensure all necessary personnel are able to perform to PMG standards.
* Assisting with the evaluation of employees through performance assessments.
* Reporting to management in regards to operational issues.

What you will have:

  • Required Education and Experience: 4 year degree or equivalent preferably within Biology, Pharmacology, or a health-related field of study.
  • Minimum of 3 years of experience in a clinical research environment. Previous supervisory/management experience strongly preferred.

#LI-Accellacare

 

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