At RayzeBio, every day is an opportunity to ignite meaningful change. As a wholly‑owned subsidiary of Bristol Myers Squibb, RayzeBio blends the nimble, pioneering spirit of an emergent biotech with the global expertise and resources of a leading innovator in oncology. Our mission is to develop transformative radiopharmaceutical therapies that offer new hope for patients living with cancer. Here, you’ll join a multidisciplinary team where your ideas are valued, your expertise is amplified, and collaboration is at the heart of everything we do. Job Responsibilities Acquires and utilizes knowledge of clinical trial design to develop or oversee development of specific study concept synopses and protocols. Participates in protocol review discussions concerning scientific and procedural aspects of study design. In collaboration with Medical Writing and Clinical Operations, prepares study protocols, amendments, specific sections of study manuals and investigator meeting materials, and other documents as needed with appropriate guidance and supervision. Works with medical writing vendors to coordinate writing and reviewing of protocols, ICFs, IBs and other clinical trial documents as needed. Contributes to the design, development, and review of CRFs, Data Management Manuals, and Data Analysis Plans. Reviews ongoing clinical data and interacts with CROs to ensure data queries are addressed and data is clean for database locks. Organizes and oversees Data Review Committee meetings, including preparation of slides and other review and meeting materials. With MD supervision, addresses questions regarding scientific and related procedural issues from investigators. Participates in site initiation visits and study start‑up activities. Establishes and maintains positive relationships with clinical trial investigators and site staff. Contributes to interactions with key thought leaders in gaining input on protocols and study designs and strategic direction. Contributes to the preparation and/or review of data listings, summary tables, study results, manuscripts, and scientific presentations. Assists in the preparation/review of INDs, regulatory documents, IND annual report/DSURs, Investigator Brochures, and NDAs/MAAs. Supports priorities within functional area. Anticipates moderately complex obstacles within a clinical study and, with guidance, implements solutions. May be asked to coordinate teams and provide direction. May lead two or more specific components of departmental strategic initiatives. Able to enter a new therapeutic area and summarize scientific information that is available in published literature to integrate into new study development. Excellent verbal and written communication skills and interpersonal skills are required to maintain working relationship with team members to ensure scientific integrity of clinical studies. May be sought out for advice by others within the company to help make better decisions and resolve moderately complex problems. Education and Experience Bachelor’s degree in Biological Sciences, healthcare, or a related field, with 8+ years of relevant scientific and/or drug development experience OR an MS degree with 6+ years of relevant scientific and/or drug development experience. Or PharmD or PhD with 5+ years of experience in clinical research or clinical pharmacology in a biotech/pharmaceutical company, contract research organization, or academic institution. Demonstrated ability to be a fast learner. Demonstrated ability to be flexible and adaptable to change, to move between projects easily and provide support/expertise where needed. Experienced with Microsoft Office (Excel, PowerPoint, etc.) as well as job‑related programs such as SpotFire. Knowledge of FDA, EMA and ICH regulations and guidelines. Ability to effectively collaborate cross‑functionally, across all levels of the organization. Physical Demands While performing the duties of this job, the employee is regularly required to sit, reach with hands and arms, and talk or hear. The employee must occasionally lift and/or move up to 20 pounds. Specific vision abilities required by this job include close vision and distance vision. Work Environment The noise level in the work environment is usually moderate. Compensation Overview San Diego - RayzeBio - CA: $227,418 - $275,577. Additional incentive cash and stock opportunities (based on eligibility) may be available. Benefits Health Coverage: Medical, pharmacy, dental, and vision care. Well‑being Support: Programs such as BMS Well‑Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP). Financial Well‑being and Protection: 401(k) plan, short‑ and long‑term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Equal Opportunity Employer Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, pregnancy, citizenship, marital status, gender expression, genetic information, political affiliation, or any other characteristic protected by law. #J-18808-Ljbffr