Mid-Level Clinical Site Identification and Start-Up Manager

5 days ago

🌲 North Carolina – Remote

Although this job is listed in North Carolina, this company may be open to hiring remote in other states.

💵 $64k - $79k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

👔 Manager

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

• Oversee and manage the end-to-end process of site identification, selection, and start-up activities for clinical trials • Lead the site identification and feasibility process for clinical trials • Coordinate the feasibility assessment process • Build and maintain a network of potential sites • Oversee the site start-up activities • Work closely with the regulatory and clinical teams • Track and report on site start-up progress • Continuously identify opportunities for process improvements • Monitor site-specific performance • Maintain accurate and up-to-date records for the site start-up activities • Mentor and provide guidance to junior team members

🎯 Requirements

• Bachelor’s degree in Life Sciences, Clinical Research, or related field • Relevant clinical research certifications (e.g., CCRA, CCRP) preferred but not required • Minimum of 2 years of experience in clinical trials with a focus on site identification, start-up, or site management within a CRO, pharmaceutical, or biotechnology company • Experience with regulatory submissions, IRB/IEC submissions, and site initiation processes is essential • Familiarity with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms • Strong knowledge of clinical trial regulations, ICH-GCP guidelines, and regulatory requirements for site initiation and activation • Excellent project management skills, with the ability to prioritize and manage multiple tasks and deadlines • Strong communication and interpersonal skills, with the ability to work effectively with both internal and external stakeholders • Detail-oriented with the ability to resolve issues and troubleshoot challenges during site start-up

🏖️ Benefits

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