Senior Clinical Research Associate – Psychiatry

🔥 21 hours ago

🤠 Texas – Remote

infoinfo

💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

Apply Now
Find Similar Remote Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Manage clinical research activities at investigative sites participating in Worldwide clinical studies • Identify and assess potential research sites • Coordinate study start-up activities, including regulatory documentation and contract and budget processes • Conduct PSSVs, SIVs, IMVs, and COVs • Train site personnel on protocol requirements, data collection, and safety reporting • Monitor site performance and support study maintenance activities • Ensure informed consent, safety reporting, and regulatory compliance • Partner with sites and study teams to drive data quality, participant safety, and study success • Support site closeout activities and complete study requirements

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • Experience monitoring CNS and Alzheimer's clinical trials • Requires travel within the specified region; 8–10 DOS monthly • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements • Must reside in the Central of the United States territory

🏖️ Benefits

• Competitive benefits package depending on location • Transparent compensation and pay equity

Apply Now

Similar Jobs

🕒 Yesterday

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Senior Clinical Scientist leading infectious-disease HIV clinical trials for ICON Strategic Solutions. Guiding medical monitoring, protocol execution, data review, and clinical development deliverables.

🕒 3 days ago

BioCryst Pharmaceuticals, Inc.

501 - 1000

🏥 Healthcare

💼 Consulting

📦 Logistics

Sr. Clinical Data Manager overseeing global clinical trial data management for BioCryst. Coordinating CROs, vendors, data cleaning, database locks, and regulatory submission support.

🇺🇸 United States – Remote

💰 $450M Post-IPO Debt - BioCryst Pharmaceuticals on 2023-04

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🕒 4 days ago

Regeneron

10,000+ employees

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

Senior Manager overseeing U.S. field-based Clinical Trial Liaison teams for Regeneron’s biotechnology programs. Managing trial operations, investigator relationships, performance, and site execution.

🕒 4 days ago

MSD

10,000+ employees

🏥 Healthcare

📦 Logistics

🧬 Biotechnology

Senior Clinical Research Associate monitoring cardiovascular clinical trials for Merck, a pharmaceutical company. Managing sites, compliance, regulatory documentation, and investigator relationships across assigned protocols.

🗣️🇪🇸 Spanish Required

🕒 5 days ago

ICON plc

10,000+ employees

💼 Consulting

🏥 Healthcare

📦 Logistics

Senior Clinical Research Associate monitoring medical-device clinical trials for ICON across the Central U.S. Ensuring GCP compliance, site performance, data quality, and trial execution.