Senior Clinical Research Associate jobs in United States
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Clinovo · 3 hours ago

Senior Clinical Research Associate

positionRedwood City, CA
timeFull-time
remoteHybrid
senioritySenior Level
money$140K/yr - $160K/yr
date5+ years exp

Clinovo is a company focused on clinical research, and they are seeking a Senior Clinical Research Associate responsible for clinical site management and monitoring activities. The role involves ensuring adherence to study protocols and GCP guidelines, performing monitoring visits, and collaborating with the clinical study team.

BiotechnologyHealth CareHospitalPersonal Health
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H1B Sponsor Likelynote
Hiring Manager
Adam M.
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Responsibilities

Perform on-site and remote monitoring visits for assigned sites in accordance with the Clinical Monitoring Plan, ICH GCP guidelines, and applicable local regulations
Conduct source data verification to ensure Case Report Form (CRF) data is accurate, complete, and consistent with source documents and the protocol
Manage day-to-day communication with assigned sites, supporting enrollment, query resolution, and overall site performance
Proactively identify and document site-level risks and issues, respond to study-specific questions, and manage escalations through to resolution
Oversee the collection, review, and maintenance of essential regulatory and study documents to ensure inspection readiness
Collaborate closely with investigators and internal clinical teams to support effective study start-up, conduct, and close-out, and to ensure successful trial execution
Oversee the execution of clinical trial activities in accordance with Good Clinical Practices

Qualification

Clinical trial experienceFDA regulations knowledgeICH-GCP guidelines knowledgeCCRA/CCRP certificationClinical trial management systemsMicrosoft Office proficiencyMentoring skillsCommunication skills

Required

Travel required (up to 80%)
Bachelor's degree in a life sciences or health-related field
5+ years of clinical trial experience to include study monitoring; experience with LDTs or in vitro diagnostic devices strongly preferred. 3+ years experience with a master's degree
Strong knowledge of FDA regulations, ICH-GCP guidelines, and clinical trial operations
Ability to travel frequently, sometimes on short notice, and manage travel logistics effectively

Preferred

CCRA/CCRP certification is desired
Proficiency in Microsoft Office and clinical trial management systems (CTMS) preferred

Company

Clinovo

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Clinovo provides drug development and solutions.
dateFounded in 2003
location
Kendall Park, New Jersey, USA
people-size51-200 employees
web-link
http://www.clinovo.com/

H1B Sponsorship

Clinovo has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (1)
2024 (1)
2023 (2)
2022 (1)

Funding

Current Stage
Growth Stage
Total Funding
unknown
2015-12-28Angel
2014-01-01Series Unknown

Recent News

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2022-08-19
Company data provided by crunchbase