Clinical Site Activation Specialist

IQVIA

Durham (NC)

On-site

USD 36,000 - 91,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

IQVIA, a leading global provider of clinical research services, is seeking a Site Activation Associate in Durham, NC to perform country-level activation tasks in accordance with regulations, SOPs, project requirements and budgets.

You will review regulatory documents, prepare site materials, and coordinate with the Site Activation Manager, Project Management team, and other departments to ensure timely completion and accurate records.

Qualifications

  • Bachelor's Degree Life sciences or related field.
  • 1 year experience in a healthcare environment or equivalent.
  • Good interpersonal communication and organizational skills.
  • Good MS Office knowledge.
  • General awareness of clinical trial environment and drug development process.

Responsibilities

  • Perform site activation activities in assigned studies for investigative sites, following regulations and SOPs.
  • Prepare site regulatory documents and review for completeness and accuracy.
  • Inform team of completion of regulatory and contractual documents for individual sites.
  • Distribute completed documents to sites and internal project team members.
  • Support updating and maintenance of internal systems, databases, timelines and project plans with accurate information.
  • Review, track and follow up progress, approvals and execution of documents and regulatory materials.

Skills

Interpersonal communication
Organizational skills
MS Office
Attention to detail
Multitasking
Team collaboration

Education

Bachelor's Degree Life sciences

Tools

MS Office

Job description

IQVIA, a leading global provider of clinical research services, is seeking a Site Activation Associate in Durham, NC to perform country-level activation tasks in accordance with regulations, SOPs, project requirements and budgets.

You will review regulatory documents, prepare site materials, and coordinate with the Site Activation Manager, Project Management team, and other departments to ensure timely completion and accurate records.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Site Activation Lead (Clinical Trials)
Senior Site Activation Lead (Clinical Trials)

IQVIA Inc • Durham (NC)

On-site
USD 63,000 - 157,000
Site Activation & Contracts Specialist
Site Activation & Contracts Specialist

IQVIA • Durham (NC)

On-site
USD 49,000 - 123,000
Senior Site Activation Lead
Senior Site Activation Lead

IQVIA • Durham (NC)

On-site
USD 63,000 - 157,000
Site Activation Lead — Clinical Trials
Site Activation Lead — Clinical Trials

NCBioImpact • Durham (NC)

On-site
USD 63,000 - 157,000
Site Activation & Contract Negotiation Specialist
Site Activation & Contract Negotiation Specialist

IQVIA • Lexington (KY)

On-site
USD 49,000 - 123,000
Global Site Activation Lead
Global Site Activation Lead

IQVIA Inc • Durham (NC)

On-site
USD 87,000 - 216,000
Site Activation Specialist: Start-Up & Feasibility
Site Activation Specialist: Start-Up & Feasibility

IQVIA • United States

Remote
USD 55,000 - 75,000
Site Activation & Contracts Specialist
Site Activation & Contracts Specialist

IQVIA • Indianapolis (IN)

On-site
USD 49,000 - 123,000
Global Site Activation Lead
Global Site Activation Lead

IQVIA • Durham (NC)

On-site
USD 87,000 - 216,000
Remote Site Activation Specialist for Clinical Trials
Remote Site Activation Specialist for Clinical Trials

IQVIA • United States

Remote
USD 22,000 - 36,000