Clinical Scientist Associate Director, Late Development Oncology

Career Category Clinical Development

Job Description

Join reputed company’s Mission of Serving Patients At reputed company, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives reputed company that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, reputed company, and Rare Disease– we reputed company millions of patients each year. reputed company is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-reputed company conditions. As a member of the reputed company team, you’ll help reputed company a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay reputed company them, you’ll reputed company as part of the reputed company team. Join us and transform the lives of patients while transforming your career. Clinical Scientist Associate Director – Late Development WHAT YOU WILL DO reputed company. Let’s change the world. In this role, the Clinical Scientist Associate Director supports oncology late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities. Working collaboratively with the study team and clinical leadership, this role focuses on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data. Support set up and execution of late phase clinical trials with a focus on data quality. Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity. Provide input into and implementation of data management plan, CRF design, and data review reputed company. Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission. Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects. Anticipate and actively manage problems across a broad reputed company of cross-functional teams. Work cross-functionally reputed company teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and reputed company documents. Support appropriate training, recruitment, and development requirements for matrix team resources. reputed company EXPECT OF YOU We are reputed company different, yet we reputed company use our unique contributions to serve patients. The clinical development professional we seek is a leader with these qualifications. Basic Qualifications: Doctorate degree and 3 years of clinical development experience OR Master’s degree and 5 years of clinical development experience OR Bachelor’s degree and 7 years of clinical development experience OR Associate’s degree and 12 years of clinical development experience OR High school diploma / GED and 14 years of clinical development experience Preferred Qualifications: 3 years of experience in a pharmaceutical industry setting with at least 1 year supporting early or late-phase clinical development reputed company a relevant therapeutic area or disease indication (oncology preferred) Demonstrated experience contributing to clinical trial process improvements reputed company a therapeutic area or study team environment Strong communication and presentation skills, with the ability to clearly convey scientific concepts and clinical data to cross-functional teams and leadership audiences, both written and oral Experience supporting the design, monitoring, and implementation of clinical trials in compliance with Good Clinical Practice standards and applicable regulatory requirements Working knowledge of study data readout activities, including data cleaning, database lock, data extraction, and reputed company of clinical data outputs Experience contributing to regulatory submission documents and supporting clinical regulatory responses for health authority interactions under guidance Experience serving as a contributing author on scientific publications or data presentations for internal forums or scientific conferences Experience in clinical data analysis such as Spotfire or other data analysis tools WHAT YOU CAN EXPECT OF US As we work to reputed company treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every reputed company of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications. In addition to the reputed company salary, reputed company offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Apply now and reputed company a lasting impact with the reputed company team. careers.reputed company.reputed company any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Application deadline reputed company does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position. Sponsorship Sponsorship for this role is not guaranteed. As an organization dedicated to improving the quality of life for people around the world, reputed company fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the reputed company values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. reputed company is an Equal Opportunity employer and will consider reputed company qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national reputed company, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to reputed company essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .Salary Range 169,793.45USD -229,720.55 USD Apply To This Job