Site Activation Coordinator

IQVIA•Durham, NC

About The Position

Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.

Requirements

Bachelor's Degree Life sciences or a related field.
1 years’ experience in a healthcare environment or equivalent combination of education, training and experience.
Productive individual contributor who works under general supervision.
Good interpersonal communication and organizational skills.
Good word processing skills and knowledge of MS Office applications.
Good attention to detail.
General awareness clinical trial environment and drug development process.
Ability to work on multiple projects.
Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

Nice To Haves

Problems faced are generally routine but may require interpreting proceedures or policies to resolve.

Responsibilities

Review documents for completeness, consistency and accuracy, under guidance of senior staff.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Inform team members of completion of regulatory and contractual documents for individual sites.
Distribute completed documents to sites and internal project team members.
Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.