Lead a large clinical study or a series of related studies with minimum guidance.
Provide mentoring and training to lower-level Data Management staff assigned to your studies.
Develop or lead the development of the Data Management Plan for a clinical study.
Parexel provides Clinical and Consulting solutions to the world’s life sciences industry. They have a global breadth of clinical, regulatory and therapeutic expertise, and a proven track record spanning 40+ years.
Accountable for leading assigned clinical research activities and partnering with stakeholders on study design.
Conducts on-site and remote site visits, including qualification, initiation, monitoring, and close-out.
Tracks study progress, manages budgets, and mentors junior clinical study managers.
Intuitive is a pioneer and market leader in robotic-assisted surgery, dedicated to minimally invasive care. With over 25 years of experience, the company fosters an inclusive and diverse team culture where employees are empowered to do their best work.
Perform ongoing clinical data review to ensure data quality, consistency, and completeness.
Identify discrepancies and raise/resolve queries in EDC systems.
Review patient data including eligibility, medical history, treatment, safety data, and outcomes.
Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. They partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity and anticipate change.
Ensure accuracy, consistency, and integrity of critical clinical trial data supporting life sciences and patient care.
Design, validate, and maintain project-specific clinical databases and data transfer processes.
Collaborate with clinical project teams and external partners to manage the full lifecycle of clinical data systems.
The company connects candidates with job opportunities using AI-powered matching. They process applications and share shortlisted candidates with hiring companies.
US Eastern Time ZoneUS Central Time Zone
Unlimited PTO
Conduct qualification, initiation, interim, and close-out monitoring visits (on-site and remote) in compliance with GCP, ICH, and SOPs.
Build and maintain strong relationships with investigator sites, providing training and guidance to ensure study quality.
Support IRB submissions, regulatory documentation, and trial master file quality across clinical programs.
CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. The company is a cutting-edge startup focused on improving diagnosis and treatment of brain disorders, with a culture that embraces AI in daily work.
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.