Clinical Research Associate (Level II) responsible for monitoring clinical trials, ensuring compliance with ICH-GCP and regulatory standards, conducting remote or on-site visits, and managing documentation and audit readiness.
Responsibilities
Monitors investigator sites with a risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Assesses investigational product through physical inventory and records review
Documents observations in reports and letters
Escalates deficiencies and issues to clinical management
Requirements
Bachelor's degree in a life sciences related field
Senior Clinical Research Associate (Senior CRA) at Magnus Medical, a medical device company focused on advancing treatments in mental health, responsible for overseeing the execution of clinical trials from site selection through close-out, ensuring adherence to study protocols, regulatory guidelines, and Good Clinical Practice (GCP).
Compensation
Salary Range: $140,000 - $165,000 Annually
The annual base salary range for this position based in the United States is noted. This range is an estimate, and actual salary may vary based on Magnus' compensation practices, job-related skills, depth of experience, relevant certifications and training, and geographic location. Magnus utilizes the full width of the range. Our compensation package also includes an annual bonus based on company goals and an equity grant.
Responsibilities
Independently manage clinical monitoring activities for assigned clinical trial sites including site selection/qualification, initiation, routine monitoring, and close-out visits.
Serve as a key liaison between Magnus and clinical trial sites, building strong site relationships and ensuring high engagement in trials involving sensitive patient populations.
Collaborate effectively with peers and leadership across departments and professionally interact/build relationships with investigators, key opinion leaders etc.
Ensure the accuracy and integrity of data by reviewing source documents and case report forms (CRFs), with attention to detail.
Monitor protocol compliance, subject safety, informed consent processes, and the proper administration of psychiatric scales.
Lead operational activities for clinical trials at a regional level, overseeing monitoring teams, site management, and ensuring timelines and quality standards are met.
Locations (2)
Rockville, Maryland, United States
United States
Responsibilities
Lead operational activities for a study or group of studies at a regional level
Oversee monitoring team and associated deliverables
Ensure clinical trial timelines are met and communicated
Manage site management and site monitoring activities
Provide forecast projections to GPM and track clinical team overburn/underburn
Requirements
Bachelor's Degree in Science related field
Master's Degree in Science related field
Nice to have: Master's Degree in Science related field
Nice to have: Experience as CRA or in a clinical operations coordinating role
Clinical Research Associate (CRA) responsible for monitoring and managing clinical trial sites, ensuring compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
Compensation
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
Responsibilities
Monitor investigator sites using risk-based monitoring.
Conduct on-site and remote visits to assess protocol compliance.
Review and verify data accuracy through SDR, SDV, and CRF.
Document observations and communicate findings.
Escalate deficiencies and follow up to resolution.
Requirements
Bachelor's degree in a life sciences related field or Registered Nursing certification
Clinical Research Associate (Level II) responsible for monitoring investigator sites, ensuring compliance with ICH-GCP, managing documentation, and coordinating remote or on-site visits.
Responsibilities
Monitors investigator sites with risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates deficiencies and follows issues to resolution
Maintains contact between monitoring visits and investigative sites
Requirements
Bachelor's degree in a life sciences related field
Clinical research associate responsible for monitoring investigator sites, ensuring compliance with ICH-GCP and regulatory requirements, conducting on‑site and remote visits, and managing documentation.
Compensation
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits.
Responsibilities
Monitor investigator sites using risk‑based monitoring
Conduct on‑site and remote visits to assess protocol compliance
Review data accuracy through SDR, SDV and CRF
Document observations and communicate findings
Escalate deficiencies and follow through to resolution
Requirements
Bachelor's degree in a life sciences related field
Senior Clinical Research AssociateNewMagnus Medical · US
Clinical Trial Manager INewEmmes Group · Remote, US+1 more
Licensed Practical Nurse (LPN) – Short-Term & Casual ContractsNewHealthOPM · Lethbridge, Canada+6 more