Site Identification Associate (Office-Based) - IQVIA Biotech

IQVIA Biotech, a global full service CRO providing flexible, tailored, integrated clinical solutions to smaller biotech companies, is seeking candidates with a strong interest in joining the clinical research industry for a Site Identification Associate. An ideal candidate would have some type of knowledge of clinical research from an internship, university clinical setting or completed research classes with a focus on the industry. The drive to learn, adapt and take initiative are all qualities that would fit well with this role. This position will be required to work onsite in the RTP area as circumstances move in that direction.

BASIC FUNCTIONS:

The basic function of the Site Identification Associate is to assist the Site ID Specialists in the resolution of requests associated with InfoStart, the PI Database, site metrics, pre-award outreach and site list creations.  The associate will work directly with more senior colleagues to ensure an understanding of the process and tools required to complete each deliverable.

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILIITIES:

• Become familiar with IQVIA Biotech tools such as InfoStart, IL2 and the PI Database
• Become familiar with IQVIA tools such as ISLA and SSI Macro
• Become familiar with external Site ID tools, such as Citeline
• Assist the Site ID department with the completion of infoStart request
• Assist the Site ID department with resolving site metric requests
• Support the Site ID Specialists with pre-award outreaches and site list requests
• Conduct all activities according to appropriate Biotech and/or sponsor SOPs.
• Performs other duties as required.

KNOWLEDGE, SKILLS & ABILITIES:

• Strong written and verbal communication skills to express complex ideas to team members.
• Excellent organizational and interpersonal skills.
• Positive attitude and ability to interact with all levels of staff.
• Strong technical skills for working in databases.
• Ability to manage multiple priorities.
• Demonstrated ability to use sound judgment and assess and recommend specific solutions.
• Preferred basic knowledge of the drug development process and ICH/GCP
• Ability to work independently on tasks with regular oversight and to prioritize effectively and work within a matrix team environment.
• Working knowledge of CTMS preferable.
• Working knowledge of Word, Excel and Power Point

PHYSICAL REQUIREMENTS:

• Limited travel may be required.

• Very limited physical effort required to perform normal job duties.

MINIMUM RECRUITMENT STANDARDS:

• Bachelor’s degree preferably in the field of science or clinical research, or equivalent combination of education, training and experience

CLASSIFICATION (US):

This position is classified as non-exempt under the Fair Labor Standards Act; employees are eligible for overtime compensation subject to prior approval.

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At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

IQVIA is an EEO Employer - Minorities/Females/Protected Veterans/Disabled

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.