• Chile

"Monitor onsite and remotely, verify consent procedures, maintain data integrity, write reports, prepare for audits, provide training, handle clinical tasks. Bachelor's degree required, travel necessary."

• Sao Paulo, Brazil

Perform essential document collection, review, and negotiation for site activation and maintenance. Recruit study sites and accurately track and document clinical data. Complete submissions to regulatory authorities. Maintain study documentation in a..

• US National

Support program management tasks including pharmacovigilance compliance, drug supply management, document maintenance, and due diligence. Learn to use systems for communication and planning. Adhere to processes, trainings, and SOPs for consistency an..

• Paris, France

Manage assigned clinical studies, conduct site visits, develop relationships with site staff, ensure data integrity, and attend investigator meetings. Requires 3+ years of CRA experience, organizational skills, and fluency in French and English.

• NY, NJ, PA, VA, Washington, DC

Completes monitoring activities, verifies informed consent procedures, ensures data integrity, manages site staff, writes reports, manages essential documents, performs risk assessment, participates in audits, assists with ad hoc assignments, and pro..

• IL, IN, WI, MN

Completes onsite and remote monitoring activities, verifies study participant protection, ensures data integrity, manages investigative site staff, writes reports, manages essential documents, performs risk assessment, participates in audit preparati..

• US National

Responsible for executing clinical trial contracts, negotiating scope of work and budgets with vendors, maintaining contracts database, and collaborating with cross-functional teams. Minimum 5 years of outsourcing experience required.

• Munich, Germany

Manage site payments for clinical trials, including budget management, participant travel policies, data transfer agreements, and milestone payments. Attend study program calls and provide routine updates and reports to management. Minimum 5 years of..

• ME, NH, MA, RI, CT, NY, NJ, DE, MD, VA, NC, SC, GA, FL, NB, Canada, NL, Canada, NS, Canada, PE, Canada, QC, Canada, ON, Canada

Lead and coordinate phase 1-4 clinical trials globally, manage study metrics, budgets, and vendors. Ensure compliance with regulations, train study teams, and liaise with Quality Management. 6-8 years of experience required.

• US National

Monitor study finances, lead financial review meetings, drive close-out process, provide analysis and metrics to improve financial management. BA/BS in Finance preferred, 5+ years of clinical trial budget experience required.

• Brazil

Line manage CRAs and/or CTAs, oversee site management activities, create a culture of process improvement, comply with relevant procedures and processes.

• Sydney, Australia, Melbourne, Australia

Manage study startup activities including contract and budget negotiation, ethics submissions, site monitoring, and timeline management. Provide support to a client team and contribute to the growth of the organization.

• United Kingdom, Bulgaria, Czechia, Ireland, Poland, Romania, South Africa, Spain, Slovakia

Serve as the responsible biostatistician on clinical trials. Contribute to clinical study protocols. Develops Statistical Analysis Plans and/or performs senior quality review of statistical analysis plans. Review and interpret results from simple to ..

• Belgium

Operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Ensure quality data and trial documents/records. Partner with the Study team for overall study delivery.

• Hong Kong

Monitor and manage clinical research sites, act as the main contact point for site staff, and have solid experience in site monitoring with global studies. Must be fluent in Cantonese and English with a Bachelor's Degree.

• Auckland, New Zealand

Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits and database lock. Embed in client's study team with dedicated line manager support. Ensure high quality dat..

• Argentina

Completes onsite and remote monitoring activities in accordance with guidelines and regulations. Verifies informed consent procedures and ensures data integrity. Writes reports and participates in audit preparation. Provides training and may be assig..

• Argentina

Perform feasibility, site identification, and other study start-up activities. Prepare, review, and submit submissions to ethics and regulatory authorities. Develop and finalize country-specific documents. Perform quality review of submission packages.

• US National

"Monitor clinical trial data, evaluate supplier compliance and quality, track corrective actions, develop stakeholder relationships. Requires Doctorate/Masters/Bachelor's/Associate's degree with relevant experience. Benefits offered. Emphasis on dive..

• Canada, or US National

Manage and coordinate global clinical trials, ensuring adherence to timelines, budgetary requirements, and regulatory standards. Lead the study management team, track study metrics, and ensure accurate budget management. Provide training and act as a..

• Belgium, France, Denmark, United Kingdom, Germany, Spain, Switzerland

Deliver various clinical, regulatory, and submission documents. Advise and guide clinical teams on content and processes. Drive consistency of documentation and provide recommendations for process improvements.

• Argentina

Clinical Operations Manager responsible for overseeing CRA oversight and career development, ensuring high performance and adherence to quality and performance metrics. Verify CRAs are performing to company standards and contribute to overall success..