Rho Inc

Project Associate

🇺🇸 Durham, Vereinigte Staaten Hybrid Gesundheit & Wissenschaft Vollzeit Veröffentlicht Jun 4, 2026
Arbeitsort Hybrid
Anstellung Vollzeit
Sprache English
Veröffentlicht 4. Juni 2026
Zuletzt geprüft 10. Juni 2026
JobGrid-Kontext

Rollenübersicht von JobGrid

Project Associate at Rho Inc: Durham, Vereinigte Staaten; Hybrid; Vollzeit; Gesundheit & Wissenschaft. 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: Durham, Vereinigte Staaten, Hybrid
  • Role classification: Gesundheit & Wissenschaft, Vollzeit
  • Source freshness: checked by JobGrid on 2026-06-10.
  • 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 either federally-funded or 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
  • 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