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Sponsorship verdict
Sponsorship possible
One solid signal, not two. Worth applying, and worth asking about sponsorship early.
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✓
Employer is on a government sponsor recordUSCIS Data Hub records 1 H-1B approvals for this employer in FY2023 — older 2023 data; no recent Department of Labor filings (Oct 2025 – Jun 2026) were found for it.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area.
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✓
Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Employer is on a government sponsor record
- USCIS Data Hub records 1 H-1B approvals for this employer in FY2023 — older 2023 data; no recent Department of Labor filings (Oct 2025 – Jun 2026) were found for it. Source: US Department of Labor visa filings (LCA) (US Department of Labor (OFLC), plus USCIS H-1B Employer Data Hub).
- No salary bar for this route
- H-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
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About the role
The Opportunity:
As Senior Clinical Project Associate, you will be accountable for providing clinical trial coordination
support, along with implementing operational plans in accordance with regulatory guidelines and
ICH/GCP standards. You will be an integrated member of the Relay Tx Clinical Development Operations
team making key contributions to the execution of clinical trials that will translate Relay’s innovative
science into impactful medicines for patients.
Your Role:
• You will support the day-to-day operations of clinical trial execution, with a focus on site start-up,
study participant enrollment, clinical monitoring, drug supply planning, defining clinical supply
logistics, GCP and protocol compliance, from the clinical sites, CROs and vendors.
• You will coordinate with the CRO and the Relay Tx Clinical Operations Lead to support planning from
study initiation through study closure.
• You will maintain study trackers and provide metrics as needed.
• You will review and contribute to key study documents including, but not limited to, informed
consent forms, case report forms, and study plans.
• You will assist with the preparation and distribution of meeting agendas and minutes as well as
actively participate in team meetings providing updates on your key responsibilities.
• You will help to ensure the Trial Master File is up-to-date and inspection ready.
• You will support inspection readiness by collaborating with CROs and providing support to clinical
sites to prepare for and respond to audit/inspection findings conducted by internal QA and external
regulatory agencies.
• You will actively participate in the development of department initiatives; contribute ideas to
department initiatives that will make a difference to the efficiency and effectiveness of Clinical
Operations.
Your Background:
• You have 2-3 years of experience in clinical trial experience. CRO or Sponsor experience is strongly
preferred.
• You are familiar with GCP and ICH Guidelines and the application to the conduct of clinical trials
• You are a motivated self-starter who is capable of flourishing in a fast-paced small company
environment.
• You are a creative problem-solver with excellent communication and public speaking skills.
• You are familiar with MS Office products (MS Project, Excel and Power Point)
• You have strong interpersonal and organizational skills, with a high degree of attention to detail.
• You are pragmatic and able to manage multiple projects and needs effectively
Estimated Salary Range : [ $69,000 - $99,000 ].
The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate’s education, experience, skills and location.
#BP1
About Relay Therapeutics
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.
Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in
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