Clinical Trial Associate

Amsterdam, Amsterdam, Netherlands
Full Time
Clinical Operations
Experienced
Company Overview
Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage it takes for patients and their caregivers to begin their journey of advocacy to find the answers they need. Their courage inspires us to challenge convention, ask bold questions and seek answers for them. Every day, we strive for excellence through our willingness to adapt, learn, and our tenacity to overcome barriers, together.

Opportunity Overview
The Clinical Trial Associate position will be responsible for providing operational support to Phase 1 through Phase 3 studies in rare neuroendocrine disease.  This position will report into the individual study leads to ensure key deliverables are met for each of the studies.   This is an opportunity to work across multiple phases of development on global studies and have a direct impact in helping Rhythm achieve important corporate milestones.

Responsibilities and Duties
  • Monitor drug and ancillary supplies to maintain adequate stock at sites
  • Consolidate dosing data from electronic source to ensure patient dosing compliance
  • Track clinical trial insurance and licensing agreements across studies and coordinate with vendors to keep them current
  • Manage internal approval process for contracts, purchase orders, and change orders
  • Manage Clinicaltrials.gov postings
  • Coordinate translations of study documents
  • Develop and maintain internal and external tracking tools
  • Support the development and review of study documents
  • Perform TMF quality checks
  • Coordinate study-specific training
  • Organize meetings and prepare meeting minutes
  • Support the planning and organization of Investigator Meetings
  • Review site monitoring reports

Qualifications and Skills
  • BA/BS or local equivalent in life sciences or related area preferred
  • 1+ years clinical research experience in a CRO, hospital or industry
  • Knowledge and training on GCP
  • Ability to work in a fast paced, matrix environment
  • Outstanding organizational skills and detail oriented; ability to track detailed information

More about Rhythm
We are a dynamic and growing global team spanning more than a dozen countries. At Rhythm we are dedicated to transforming the lives of patients living with rare neuroendocrine diseases by rapidly advancing care and precision medicines that address the root cause. Our team is passionate about expanding access to reach more patients and developing novel therapies for other rare neuroendocrine diseases, including congenital hyperinsulinism.  


At Rhythm our core values are:
  • We are committed to advancing scientific understanding to improve patients’ lives
  • We are inspired to tackle tough challenges and have the courage to ask bold questions
  • We are eager to learn and adapt
  • We believe collaboration and ownership are foundational for our success
  • We value the unique contribution each individual brings to furthering our mission

 
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