Description

About Ratio Therapeutics

Ratio Therapeutics is committed to improving and extending the lives of cancer patients without sacrificing their quality of life. We are a team of passionate scientists, engineers, and business professionals dedicated to advancing the field of targeted radioligand therapy to enable new therapies with higher cure rates and fewer side effects. To accomplish this, we utilize our proprietary TRILLIUM™ and MACROPA™ platforms:  TRILLIUM™ allows fine-tuning of radioligand pharmacokinetics thereby enhancing the therapeutic index, while MACROPA™ simplifies the manufacturing process for the alpha-emitting isotope, actinium-225. These enabling platform technologies have resulted in an emergent pipeline of novel therapeutic candidates. We are looking for talented, dedicated, and creative individuals eager to help us advance these technologies from discovery research through clinical development. Join us in our quest to become the leading innovator in radioligand therapy and improve the lives of cancer patients and their families.

About the Position

Ratio is seeking a Clinical Operations Lead to join a growing team of scientists responsible for overseeing the planning, execution, and tracking of clinical studies from start to finish. The ideal candidate will have a strong background in clinical research and project management and will be able to effectively lead cross-functional teams to ensure that all study-related activities are completed on time, within budget, and in accordance with regulatory requirements. The successful candidate will be a driven and highly motivated individual with a passion for clinical research and a commitment to excellence who enjoys working in a collaborative, fast-paced environment. This position holds significant growth potential, a successful candidate would have the opportunity to build the department with additional team members.

Key Responsibilities

• Develop and manage standard operating procedures, clinical study protocols, timelines, budgets, and resources
• Oversee the selection and management of clinical research sites, contract research organizations (CROs) and vendors, from study start-up to close out
• Ensure that all study-related activities are conducted in compliance with regulatory requirements and meet Good Clinical Practice (GCP) guidelines
• Collaborate with cross-functional teams, including clinical operations, data management, biostatistics, medical writing, and regulatory affairs, to ensure that studies are conducted effectively and efficiently
• Develop and implement risk mitigation strategies to minimize disruptions to study timelines and budgets
• Communicate study progress and results to senior management and key stakeholders

Requirements

Qualifications

• Bachelor's degree in a related field (e.g., life sciences, nursing, public health, etc.)
• Minimum of 5+ years of experience in clinical operations and project management or equivalent
• Strong knowledge of clinical research processes and regulatory requirements
• Excellent project management, organizational, and time-management skills
• Excellent verbal and written communication skills
• Ability to work independently and as part of a team
• Familiarity with clinical trial management systems and project management tools