
1 - 10 employees
Transcend Therapeutics, founded in 2021, is a clinical-stage, neuroscience-focused company developing rapid-acting treatments for neuropsychiatric diseases. Our mission is to develop new drugs for the millions of people for whom current psychiatric medicines have not worked. Our leadership team has made pivotal contributions to 13 FDA approvals (including recent MDD approval), $3.5B in M&A, and significant public company value creation.
🕒 March 19
Improve your chances of getting an interview by checking your resume score before you apply.

1 - 10 employees
Transcend Therapeutics, founded in 2021, is a clinical-stage, neuroscience-focused company developing rapid-acting treatments for neuropsychiatric diseases. Our mission is to develop new drugs for the millions of people for whom current psychiatric medicines have not worked. Our leadership team has made pivotal contributions to 13 FDA approvals (including recent MDD approval), $3.5B in M&A, and significant public company value creation.
• Perform on-site monitoring visits, such as evaluation visits, SIV, IMV, and COVs along with timely and comprehensive site visit reports. • Ensure site maintains an accurate inventory and accountability of investigational drug and clinical supplies. • Ensure sites are conducting the study according to the protocol with high-quality data collection processes and excellent attention to patient safety. • Coordinate with the in-house team to provide ongoing site support. • Coordinate with the in-house team to maintain site compliance with study timelines, metrics, and plans. • Identifies and communicates trends, risks, and deviations. Facilitate resolution of problems, queries and action items including identification of cause and actions to prevent recurrence. • Support and train other CRAs, as needed. • Support the in-house team as needed (eg, recruitment strategies, UAT of CRFs, remote data review). • All other duties as required.
• Bachelor’s degree, preferably in a life science • At least 4 years of clinical trial experience within a pharmaceutical company or CRO, including at least 2 years of on-site monitoring experience and experience with risk-based and hybrid monitoring models. • Strong understanding of clinical quality assurance principles and practices is preferred • Experience in conducting studies in psychiatry-related indications is preferred • Proficient knowledge of GCP/ICH, drug development process, clinical operations
• Competitive cash and equity compensation • Medical, dental, and vision insurance • 401k • Unlimited vacation and sick time • More
Apply Now🕒 March 5
Contract Clinical Research Associate overseeing clinical trial protocols and site management for Freenome. Managing compliance and monitoring while contributing to cancer diagnostics research.
🇺🇸 United States – Remote
💰 $290M Corporate Round on 2022-01
⏳ Contract/Temporary
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🦅 H1B Visa Sponsor