Rho Inc

Project Associate

🇵🇱 Remoto, Polonia Remoto Salud y ciencia Jornada completa Junior Publicado May 19, 2026
Ubicación Remoto, Polonia
Modalidad Remoto
Contrato Jornada completa
Seniority Junior
Categoría Salud y ciencia
Idioma English
Publicado 19 de mayo de 2026
Última verificación 29 de mayo de 2026
Contexto de JobGrid

Resumen del puesto por JobGrid

Project Associate at Rho Inc: Remoto, Polonia; Jornada completa; Junior; Salud y ciencia. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Remoto, Polonia
  • Role classification: Salud y ciencia, Jornada completa, Junior
  • Source freshness: checked by JobGrid on 2026-05-29.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

Join us in redefining what it means to work for a CRO. Working at Rho, you’ll be joining a team who take healthcare and clinical research personally, with shared experiences that drive a passion to heal, cure and solve some of humanity’s biggest challenges.

At Rho, you’ll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career. With a collaborative team of smart, talented, and positive people, you’ll be celebrated and respected for your expertise and given the freedom to think creatively, challenge the norm, and problem-solve.

As a Project Associate, you will have the opportunity to gain the necessary experience and opportunities to grow your career in Clinical Research! You will assist project managers in day-to-day operations of commercial studies.  Please note that this is an entry-level position and it is not a laboratory research position.

Our Study Teams will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!

The position will offer the opportunity to participate in all aspects of clinical research support, including document preparation, maintenance, and filing; meeting coordination and support; and data management activities including data entry and review.  More specifically, the position may also include the following responsibilities:

  • Writing external correspondence, such as emails, memos, minutes and reports
  • Formatting documents and creating document templates
  • Support Study Team to track the study status, materials, system accesses and study team trainings
  • Creating and formatting Case Report Forms, manual of operations documents, and other study-related documentation
  • Maintaining project website
  • Communicating with internal and external project staff