SonicJobs Logo
Left arrow iconBack to search

Study Startup Specialist I

PSI CRO
Posted a month ago, valid for 12 days
Salary

Competitive

Contract type

Full Time

By applying, a PSI CRO account will be created for you. PSI CRO's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • PSI is a leading Contract Research Organization with over 30 years of experience in the industry, emphasizing quality and timely services.
  • The position involves supporting study startup processes in the US, ensuring smooth and timely project initiation.
  • Candidates should have at least 1 year of industry experience in clinical research or study startup.
  • The role includes maintaining project-specific tracking systems and providing administrative support for site agreements and budgets.
  • Salary information is not provided, and PSI is not hiring individuals requiring work visas for this position.

Company Description

PSI is a leading Contract Research Organization with more than 30 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

Take your career to the next level and be involved in study startup processes in the US. You will provide direct operational support to project teams and ensure that PSI clinical projects start smoothly and on time. 

You will:

  • Supports all processes critical for site activation.
  • Supports Feasibility department with feasibility research and site identification process.
  • Maintains project-specific tracking systems and electronic Trial Master File (eTMF) throughout study startup phase.
  • Provides administrative support with site agreement and budgets.
  • Assists with site documents collection for IRB/IEC submission and/or IP-RED process.
  • Provides progress updates to all concerned functions.
  • Identifies project-specific issues and escalates as outlined in the project specific Communication Plan.
  • Supports preparation of study dossiers to sites and competent authorities.
  • Supports preparation of IP-RED packages.
  • Ensures exchange of information and documentation with investigational sites, off -site facilities and vendors throughout study startup phase.
  • Additional responsibilities may include collecting documents in preparation for audits on a country-region level.

Qualifications

  • College/University degree or an equivalent combination of education, training and experience
  • At least 1 year industry experience in clinical research and/or a minimum 1 year of Study Startup experience​
  • Communication and organizational skills
  • Ability to negotiate and build relationships at all levels

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.

For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.




Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a PSI CRO account will be created for you. PSI CRO's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.