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Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the care of people living with rare melanocortin-4 receptor (MC4R) pathway diseases. Working at Rhythm means that you are part of a team that’s passionate about transforming the lives of people living with hyperphagia (pathological, insatiable hunger) and severe obesity caused by rare MC4R pathway diseases.
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 and learn, and our tenacity to overcome barriers, together.
Opportunity Overview
As a Clinical Trial Associate, you will be responsible for providing operational support to Phase 1 through Phase 3 studies of setmelanotide in genetic obesity. This position will work closely with 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 and place orders with the central depot to ensure adequate stock at sites
- Consolidate dosing data from electronic sources to ensure patient dosing compliance
- Monitor clinical trial Insurance and license agreements across studies and work with vendors to ensure current agreements
- Manage internal process for approval of contracts, purchase orders, and invoices
- Facilitate shipment of various samples defined in the protocols to third-party labs
- Manage Clinicaltrials.gov postings
- Manage translations of study documents
- Develop and maintain internal and external trackers
- Assist in the development of study documents, including study and lab manuals
Qualifications and Skills
- BA/BS in life sciences or related area
- 1-2+ years of 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
