Assistant Clinical Study Manager

March 21

Apply Now

Receive Emails with Similar Jobs

RTI International

WebsiteLinkedInAll Job Openings

RTI International is an independent scientific research institute dedicated to improving the human condition through diverse services and capabilities, including public health, education, and environmental sciences. They partner with the U. S. government, universities, and various organizations to conduct research and provide solutions in areas such as health care quality, economic development, energy efficiency, and innovation in multiple sectors. RTI focuses on evidence-based strategies and data-driven solutions to address critical global challenges.

health research • drug discovery and development • education research • social and economic policy research • surveys and statistics

5001 - 10000 employees

Founded 1958

⚕️ Healthcare Insurance

📚 Education

🔬 Science

📋 Description

• Assist and support in the planning and execution of complex clinical trials. • Manage components of projects under the direction of the Lead CSM. • Assist in preparation and oversee distribution of study documents and materials. • Assemble and distribute study supplies and data collection forms to clinical sites. • Coordinate and schedule conference calls; write and distribute meeting minutes. • Manage correspondence and project communications. • Assist in preparation and updating of progress reports and client/study/network meeting materials. • Assist with preparation of site or investigator training materials; participate and assist with trainings for clinical study staff. • Collaborate with data management team to develop data collection/management strategies. • Participate in quality control activities. • Monitor risks and implement mitigation strategies. • Gather background data to support proposal and project efforts.

🎯 Requirements

• Bachelor's Degree and 3 years of experience, Master's degree and 1 year of experience, or equivalent combination of education and experience. • Strong knowledge of clinical trial drug development processes. • Experience supporting clinical trial operations. • Previous clinical site level trial management experience is a plus. • Proficiency with MS Word, Outlook, PowerPoint, Excel. • Demonstrated interest in health or clinical research. • Ability to work in a highly collaborative environment. • Ability to listen and communicate well both verbally and in writing. • Ability to synthesize and summarize complex information. • Ability to work independently. • Attention to detail and accuracy. • Ability to handle regular changes to priorities and multiple tasks ongoing simultaneously. • Reliable and predictable attendance.

🏖️ Benefits

• Competitive base salary. • Generous paid time off policy. • Merit-based annual increases. • Bonus opportunities. • Robust recognition program. • Competitive insurance plans (health, dental, life). • Access to retirement savings program (401(k)). • Paid parental leave for all parents. • Financial assistance with adoption expenses or infertility treatments. • Financial reimbursement for education and developmental opportunities. • Employee assistance program. • Other offerings to support a healthy work-life balance.