Senior Study Startup Specialist

PSI CRO

$80K — $110K *
US-AnywhereRemote in Alabama, US
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • University/college degree or equivalent education and experience
  • At least 4 years experience in clinical research
  • Minimum 3 years of comprehensive Study Startup experience

Responsibilities

  • Coordinate study startup activities and support site activation processes
  • Lead feasibility research and site identification activities
  • Facilitate site agreement and budget negotiations
  • Manage site document collection for IRB/IEC submissions
  • Review study-specific translations
  • Identify and escalate project-specific issues as necessary
  • Prepare and submit study dossiers under supervision
  • Ensure quality of IP-RED packages
  • Distribute clinical study supplies and supervise initial product distribution
  • Develop site-specific startup timelines and enrollment projections
  • Provide startup-related training and support to operational staff
  • Coach department staff and prepare audits

Benefits

  • Focus on professional development and success
  • Balance between stability and innovation in the workplace
  • Engagement in diverse therapeutic indications
Full Job Description
Company Description

PSI is a leading Contract Research Organization with more than 28 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description
  • Coordinates study startup activities with the local project team and supports all processes critical for site activation.
  • In the absence of stand-alone feasibility function, leads activities in feasibility research and site identification process.
  • Facilitates site agreement and/or budget negotiations with sites to ensure alignment to the site activation plan.
  • Leads site document collection for IRB/IEC submission and/or IP-RED process.
  • Reviews study-specific translations.
  • Identifies project-specific issues and escalates to Regional (Startup) Lead/PM and operational Manager in the country.
  • Under supervision prepares and submits the study dossiers to investigators/institutions, competent authorities, IRBs/IECs.
  • Ensures quality of IP-REDs packages.
  • Ensures initial distribution of locally obtained clinical study supplies to sites and supervises initial distribution of Investigational Product(s) and centrally obtained clinical study supplies to sites.
  • Develops site-specific startup timelines and enrolment projections and is responsible for meeting the site activation targets under supervision.
  • Provides startup-related training and methodological support to operational staff within the country/region.
  • Provides on-the-job coaching of department staff.
  • Supports preparation for audits on a country /regional level.
  • Upon completion of the project startup phase, supports the preparation of a summary on operational challenges, best practices and lessons learned, and reports to Study Startup management and other functions concerned.


Qualifications
  • University/college degree, or an equivalent combination of education, training, and experience
  • At least 4 years' experience in clinical research.
  • At least 3 years of full-scope Study Startup experience


Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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