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Study Startup Specialist II - Remote

Posted 2 days ago
All others
Full Time
Worldwide

Overview

The Study Startup Specialist II coordinates critical activities for site activation in clinical research, ensuring timely and effective startup processes.

In Short

  • Coordinates study startup activities critical for site activation.
  • Supports Feasibility department.
  • Facilitates site agreement and/or budget negotiations.
  • Collects site documents for IRB/IEC submission and/or IP-RED process.
  • Coordinates translation and reviews.
  • Supports initial distribution of Investigational Product(s) and clinical study supplies to sites.
  • Prepares and submits study dossiers to sites and competent authorities.
  • Supports study supplies distribution to sites.

Requirements

  • College/University degree in Life Sciences or equivalent.
  • At least 2 years of full-scope Study Startup experience.
  • Well-developed communication and organizational skills.
  • Ability to negotiate and build relationships at all levels.

Benefits

  • Excellent working conditions.
  • Extensive training and friendly team.
  • Competitive salary and benefits package.
  • Opportunities for personal and professional growth.
PSI CRO logo

PSI CRO

PSI CRO is a prominent Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Founded in Switzerland, PSI is a privately owned, full-service CRO that operates globally, supporting clinical trials across various countries and continents. The company is known for its selective approach to project engagement, emphasizing high-quality and timely services across a wide range of therapeutic areas. PSI values diversity and inclusivity within its workforce, fostering an environment where all colleagues feel welcomed and valued. The organization is dedicated to not only conducting clinical trials but also building a community that empowers team members to thrive and contribute to significant advancements in the pharmaceutical sector.

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