Senior Clinical Research Associate – CNS
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Senior Clinical Research Associate managing CNS clinical trial sites for Worldwide Clinical Trials, a global CRO. Overseeing study start-up, site maintenance, compliance, and closeout activities.
Responsibilities:
- Manage research activities at sites participating in Worldwide’s clinical research projects
- Identify potential sites to participate in research efforts
- Perform study start-up activities, including collecting regulatory documents
- Support negotiation of contracts and budgets
- Train sites to collect data properly and report potential safety-related events
- Manage site activities during study maintenance
- Close down research activities at sites after study conclusion
- Conduct study initiation visits (SIVs)
- Ensure compliance with informed-consent procedures, safety-event reporting, and applicable regulatory requirements
- Travel regionally as required
Requirements:
- Excellent interpersonal, oral, and written communication skills in English
- Superior organizational skills with attention to detail
- Ability to work with little or no supervision
- Proficiency in Microsoft Office, CTMS, and EDC Systems
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in CNS/Neurology is required
- Must reside in the Central United States
- Willingness to travel regionally required
Benefits:
- Extensive support through regulatory submissions, TMF management, and in-house CRAs
- Regular touchpoints and coaching conversations with the Line Manager
- Clear career path and professional development leading to Clinical Trial Manager roles
- Supportive, team-oriented environment
- Competitive benefits package depending on location
- Transparent compensation and pay equity
Similar Jobs
In-House Clinical Research Associate II
In-house Clinical Research Associate supporting site management and data-quality activities for Worldwide Clinical Trials, a global contract research organization. Coordinating clinical-study documentation, monitoring support, queries, recruitment, and site communications.
Clinical Research Associate 2
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study delivery.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate monitoring oncology trials for ICON, a global clinical research organisation. Conducting site visits, ensuring compliance, and overseeing patient safety, data quality, and site performance.
Clinical Research Associate – Oncology
Clinical Research Associate monitoring oncology and hematology trials for ICON, a global clinical research organization. Conducting site visits, ensuring compliance, and supporting patient safety and data quality.
Local Clinical Trial Manager – Single Sponsor
Clinical Trial Manager responsible for site management and monitoring in drug development at Syneos Health. Ensuring compliance and data integrity for clinical trial deliverables.
Senior Clinical Trial Manager
Senior Clinical Trial Manager overseeing and coordinating clinical trials at Sitero, ensuring compliance and project milestone achievements.
Senior Clinical Trial Manager
Senior Clinical Trial Manager at Sitero overseeing clinical trials and ensuring compliance with regulatory standards. Managing project plans, budgets, and cross-functional teams in clinical operations.
Clinical Trial Manager II
Clinical Trial Manager overseeing Phase 1 clinical research studies for Syneos Health. Collaborating with cross-functional teams to ensure patient safety and regulatory compliance.
Clinical Trial Manager
Clinical Trial Manager managing clinical trial operations within ICON to deliver high-quality outcomes across clinical programmes. Collaborating with cross-functional teams and ensuring compliance with ethical guidelines.
Application Scientist, Clinical Genomics
Join Saphetor as an Application Scientist in Clinical Genomics. Support customers through their journey with VarSome suite while collaborating globally.
Application Scientist – Clinical Genomics
Application Scientist supporting customers in Clinical Genomics with VarSome bioinformatic tools from pre-sales to post-sales. Collaborate on customer evaluations and onboarding for optimal use of the platform.
Clinical Trial Manager
Clinical Trial Manager managing clinical trial operations for ICON, a global healthcare research organization. Collaborating with teams to deliver high-quality outcomes across clinical programmes.
Principal Biostatistician, Sr Biostatistician – R/Rshiny
Principal Biostatistician role supporting drug development projects at Syneos Health. Involved in clinical data analysis, training, and statistical planning across EMEA.
Reporting Clinical Genomics Scientist – HCT
Entry level reporting position interpreting diagnostic test results for genetic counselors. Involves summary of clinical information and applying variant classification guidelines.
Clinical Trial Manager II
Clinical Trial Manager II overseeing clinical trials in dermatology and rheumatology at Indero. Managing clinical monitoring deliverables and ensuring quality in clinical research operations.
Clinical Trial Manager
Clinical Trial Manager overseeing studies for precision oncology company Guardant Health. Leading planning and execution of clinical trials from start to finish, ensuring compliance with GCP and regulatory requirements.
Trial Delivery Specialist – Clinical Trial Coordinator
Clinical Trial Coordinator delivering administrative and technical support in clinical trials globally, ensuring project activities progress efficiently within established timelines.
FSP Feasibility Manager
Feasibility Manager leading strategic and operational feasibility activities at Thermo Fisher Scientific. Driving country selection, recruitment planning, and enrollment forecasting for clinical trials.
Senior Clinical Trial Manager, Cardiac Catheter Products
Sr. Clinical Trial Manager managing global clinical trials for Catheter Ablation projects at Pulse Biosciences. Collaborating with teams to ensure data quality and compliance in a fast-paced environment.
Senior Clinical Research Counsel
Senior Clinical Research Counsel managing a wide range of contracts for clinical trials at ImmunityBio. Drafting, reviewing, and negotiating clinical trial agreements and ensuring compliance with regulations.