Senior Clinical Research Associate (CRA) - Texas or Arizona

MapLight Therapeutics•Texas, TX

7d•$145,000 - $160,000•Remote

About The Position

MapLight Therapeutics is a clinical stage biotech company focused on drug discovery for central nervous system disorders. We utilize cutting-edge technologies such as optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies for psychiatric symptoms. This is a remote role based in the Texas or Arizona region, requiring up to 75% travel, with potential for higher travel during peak activity. Travel will primarily be regional but may occasionally extend beyond the region. Periodic travel for meetings is also expected.

Requirements

Approximately 5 plus years in the clinical trial industry with at least 4 years of clinical monitoring experience including complex therapeutic areas, in-patient trials, and blinded trials.
Experience managing multiple Investigator sites and multiple studies simultaneously.
Willingness to travel nationally to assigned Investigator sites as needed for required visits.
Ability to build relationships between Investigator sites and MapLight to foster strong collaboration, trust, and positive working relationships.
Strong working knowledge of Good Clinical Practices (GCPs), ALCOA+, and pertinent regulations.
Ability to engage collaboratively with internal and external stakeholders in a professional manner.
Strong interpersonal, oral, and written communication skills.
A self-starter with the ability to work independently and proactively.
Willingness to be a “team player” and take on additional responsibilities as requested.
Demonstrates core understanding of medical terminology and clinical trial activities in relation to execution of a clinical development plan.
High attention to detail and focus on quality and compliance in all aspects of assigned work.
Experience working in various clinical software systems (EDC, CTMS, eTMF, eCOA, EMR).
Proficiency with Microsoft Office applications (Word, Excel, PowerPoint, Outlook).
Ability to travel independently by air, car and/or train.
Location near a major airport preferred.

Nice To Haves

CNS and/or neuropsychiatry, specifically in-patient schizophrenia and/or Alzheimer’s disease psychosis or Alzheimer's disease agitation experience strongly preferred.
Experience working in small/emerging biotech is ideal.

Responsibilities

Perform quality and compliant Investigator site monitoring and relationship-driven Investigator site management in line with MapLight’s SOPs, Mission, Vision, and Values, and industry quality and regulatory best practices (ICH GCP).
Conduct on-site monitoring and centralized monitoring to ensure subject safety, data integrity, and contribute to proactive risk management and inspection readiness.
Collaborate with key cross-functional internal stakeholders (Clinical Operations, Medical Monitoring, Data Management, Supply Chain, Clinical Compliance and Quality) and external CRO and vendor partners to ensure quality study oversight from study start-up through close-out.
Effectively manage assigned Investigator sites and maintain positive relationships with site personnel.
Prepare for and conduct Pre-Study, Initiation, Interim, and Closeout monitoring visits in accordance with MapLight SOPs, regulatory requirements, and industry guidelines (ICH GCP).
Support the study team in meeting study milestones (site activation, DSMB meetings, database lock, etc.).
Perform centralized monitoring activities between on-site visits to ensure timely resolution of action items, oversight of study data quality and flow, and proactively identify and mitigate/manage study risks and issues.
Maintain quality and compliant documentation related to site management, including monitoring visit reports, centralized monitoring reports, site contact reports, and Trial Master File/Investigator Site File.
Serve as the main MapLight point of contact for Investigator sites to support protocol compliance, communications, responses to site staff needs, and training.
Support the study team and Investigator sites during inspections or audits.
Perform other assigned tasks as requested.
Support the study team(s) in development of study documents and procedures.
Support the development and maintenance of the study monitoring plan, templates, and tools.
Support the set-up, testing, and maintenance of study systems (EDC, eCOA, IRT, etc.) and related supporting documents.
Continually review and reconcile the Trial Master File and Investigator Site File for assigned sites to ensure inspection readiness.
Maintain current knowledge of regulatory requirements and industry best practices related to monitoring, including centralized and risk-based monitoring.
Support development and process improvement for the MapLight monitoring function.
Support development and revision of SOPs, processes, templates, tools, and plans for continual improvement and streamlining.
Contribute to the maintenance and improvement of clinical systems to drive process improvement and efficiency.
Embody and demonstrate MapLight’s core values of Integrity, Collaboration, Bravery, and Dedication.