Clinical Research Coordinator

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

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Salary

$87K-$109K not verified - source not recorded; timestamp not recorded

401(k) match

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Market context

U.S. role benchmark (BLS OEWS)

$111,944 U.S. median for this role

Projected growth (BLS Employment Projections)

+13.7% - Much faster than average

12% below the BLS role benchmark for data and ml aggregate.

Matched to SOC 15-1252 - Data and ML aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Schedule

Shift type

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Weekend work

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Application

Cover letter

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Assessment

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Deadline

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Where they hire

State eligibility is not yet verified.

About this role

Clinical Research Coordinator Remote, USA Omada Health is on a mission to bend the curve of chronic disease. Job overview: Omada is hiring a Research Coordinator to support the Clinical Research Team team. This role is responsible for coordinating activities for research studies, implementing clinical research protocols and maintaining quality and timeliness in the execution of projects. This is a full time position and is remote. Your Impact: - Support Omada's research program by coordinating day‑to‑day study operations for assigned protocols, including tracking enrollment targets, participant flow, and key milestones. - Contact study participants to facilitate timely, complete and accurate participation in study. - Respond to questions and requests from research participants, escalating complex or clinical issues to the appropriate team member per protocol. - Coordinate transfer of data between company and collaborating institutions, following data‑handling and privacy procedures. - Maintain accurate study documentation and trackers (e.g., enrollment logs, contact logs, data transfer records) so the team has a current view of study status. - Monitor day‑to‑day study progress, proactively flag risks to timelines or data quality, and recommend practical options to keep the work on track. - Participate in regular study team meetings and status reviews, providing clear updates on your assigned workstreams and dependencies. You will love this job if you have/are: - Motivated by contributing to evidence that improves care for people living with obesity‑related and cardiometabolic conditions. - A self-starter who can organize your work, ask clarifying questions, and follow through reliably on commitments. - Comfortable

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