Senior Clinical Research Associate
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Senior CRA overseeing oncology clinical trials for Worldwide Clinical Trials, a global contract research organization. Managing investigative sites, monitoring visits, compliance, and study delivery across the Midwest.
Responsibilities:
- 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 provide ongoing support during study maintenance
- Ensure informed consent, safety reporting, and regulatory compliance
- Partner with sites and study teams to support data quality, participant safety, and study success
- Support site closeout and completion of study requirements
- Travel to investigative sites and collaborate with sites, sponsors, and global study teams
Requirements:
- Bachelor's Degree or a Nursing Degree
- 5+ years as a regional, traveling Clinical Research Associate
- 2 years of required experience monitoring Oncology clinical trials
- Requires travel within the specified region; 8–10 days of service monthly
- Experience in full-service monitoring preferred
- Strong knowledge of clinical trial processes, site management, and regulatory requirements
- Candidates must reside within the Midwest territory
- Ability to travel to investigative sites approximately 8–10 days per month
Benefits:
- Competitive benefits package depending on location
- Inclusive and equitable workplace
- Equal employment opportunities
- Transparent compensation and pay equity
Similar Jobs
Clinical Research Team Lead, Regulatory
Clinical research regulatory lead overseeing oncology trial compliance at University of Cincinnati Cancer Center. Guiding regulatory teams, protocol activation, IRB coordination, and CTMS documentation.
Principal Clinical Data Manager
Principal Clinical Data Manager leading clinical data management for Worldwide Clinical Trials, a global CRO. Overseeing complex trials, data quality, database lock readiness, and sponsor collaboration.
Freelance Senior Clinical Research Associate
Senior Clinical Research Associate conducting site monitoring and ensuring ICH-GCP compliance for PSI’s global clinical trials. Supporting investigators, trial documentation, audits, and participant safety.
Senior Clinical Research Associate – Oncology
Senior CRA conducting oncology clinical trials for Worldwide Clinical Trials, a global CRO. Managing site monitoring, regulatory compliance, and study delivery across the Western United States.
Senior Clinical Research Associate – Oncology
Senior CRA overseeing oncology clinical trials for Worldwide Clinical Trials, a global contract research organization. Monitoring sites, ensuring compliance, and supporting study delivery across the Central U.S.
Senior Clinical Research Associate – Oncology
Remote oncology Clinical Research Associate managing site operations, regulatory compliance, and study initiation for Worldwide Clinical Trials, a global clinical research organization.
Senior Clinical Research Associate – Oncology
Senior CRA overseeing oncology clinical trials for Worldwide Clinical Trials, a global contract research organization. Managing site monitoring, compliance, data quality, and regional investigative-site relationships.
Senior Clinical Research Associate – Oncology
Senior CRA monitoring oncology clinical trials for Worldwide Clinical Trials, a global CRO. Managing investigative sites, regulatory compliance, data quality, and safety across the Northeast.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring UK oncology clinical-trial sites for global CRO Worldwide Clinical Trials. Leading site activities, CRA coordination, compliance, and study delivery.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring oncology clinical trials for global CRO Worldwide Clinical Trials in Germany. Leading site activities, mentoring CRAs, and ensuring GCP-compliant study delivery.
In-house CRA I / In-house CRA II
In-house CRA supporting Precision for Medicine’s oncology and rare disease clinical trials. Managing centralized documentation, eTMF/CTMS data, reconciliations and study metrics remotely from Poland.
Senior Clinical Trial Manager
Clinical trial manager leading global Phase 0–4 studies for AbbVie, a pharmaceutical company developing innovative medicines. Overseeing vendors, recruitment, risks, systems, and study execution.
CRA 2
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and research organization. Ensuring compliance, data integrity, patient safety, and quality study documentation.
Junior Clinical Research Associate
Clinical Research Associate conducting site monitoring and clinical data review across China. Supporting ICON’s sponsor-dedicated clinical research programs and treatment development.
Clinical Research Associate II
Clinical Research Associate monitoring clinical sites and patient safety for BeOne, a company developing cancer medicines. Managing compliance, data quality, training, and study milestones.
Senior Clinical Research Associate
Senior Clinical Research Associate overseeing clinical trial sites for AbbVie, an innovative medicines company. Managing monitoring, compliance, recruitment, risk assessment and site partnerships.
Risk Manager – Clinical Research
Risk Manager developing risk-based monitoring strategies for Indero, a dermatology and rheumatology clinical research CRO. Supporting data integrity, regulatory compliance, and cross-functional trial delivery.
Clinical Trial Manager
Clinical Trial Manager overseeing clinical trial planning, execution, compliance, and delivery for ICON’s global healthcare intelligence and research organization.
Senior Clinical Research Associate
Senior Clinical Research Associate advancing Novartis Phase I–IV clinical trials through site monitoring. Managing investigator relationships, compliance, patient safety, and reliable trial data across the U.S.
Hungarian to English Translator, Pharmacovigilance, Serious Adverse Event Form (SAE)
Freelance translator converting Hungarian pharmacovigilance and SAE documents into English for TransPerfect. Certification may lead to upcoming translation projects.