Associate Medical Science Director – Late Development, Oncology
Join to apply for the Associate Medical Science Director – Late Development, Oncology role at BioSpace .
What You Will Do
In this vital role you will contribute to late phase clinical development of oncology compounds from first‑in‑human studies through proof of concept, collaborating with teams to support the definition, design, and delivery of late phase clinical and translational projects. The Associate Medical Scientific Director will support protocol development, study start‑up, data review and monitoring, and analysis activities.
Responsibilities
- 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 the data management plan, CRF design, and data review oversight
- Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
- Assist Development Lead and Medical Sciences Director in medical monitoring and management of oncology phase 3 collaborators, consultants, and / or Clinical Research Organizations in completion of key projects
- Anticipate and actively manage problems across a broad spectrum of cross‑functional teams
- Work cross‑functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol, and related documents
- Support appropriate training, recruitment, and development requirements for matrix team resources
What We Expect Of You
The dynamic professional we seek is a leader with the following qualifications.
Basic Qualifications
Doctorate degree and 3 years of clinical research experienceMasters degree and 5 years of clinical research experienceBachelors degree and 7 years of clinical research experienceAssociates degree and 12 years of clinical research experienceHigh school diploma / GED and 14 years of clinical research experiencePreferred Qualifications
3 years of pharmaceutical clinical drug development experienceIndustry or academic experience in late‑phase oncology drug developmentExperience cleaning or managing data for a Phase 3 clinical study or regulatory filingProven ability to think creatively and develop innovative strategies beyond standard clinical scientist approachesDemonstrated initiative and problem‑solving skills in dynamic, cross‑functional team environmentsExtensive experience monitoring, cleaning, reviewing clinical trial data and developing medical data review plansExperience serving on cross‑functional teams and demonstrated ability to collaborate with clinical ops through the conduct of a studyExperience in clinical data analysis such as Spotfire or other data analysis toolsBenefits
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 accountsA discretionary annual bonus program, or for field sales representatives, a sales‑based incentive planStock‑based long‑term incentivesAward‑winning time‑off plansFlexible work models, including remote and hybrid work arrangements where possibleApplication
Apply now and make a lasting impact with the Amgen team. In 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 : Amgen 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.
Equal Opportunity Employer
Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, 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 perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
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