Remote

Reimagine the infrastructure of cancer care within a technology and science community that values integrity, inspires growth, and is uniquely positioned to create a more modern, connected oncology ecosystem. We’re looking for an oncology clinical research expert to help us accomplish our mission to improve and extend lives by learning from the experience of every person with cancer. Are you ready to be the next changemaker in cancer care?

What You'll Do

As a member of the Research Oncology team that supports our Clinical Research unit, you will help develop and oversee Flatiron-led, technology enabled, pragmatically designed clinical trials. You will provide clinical and research leadership to our multifunctional teams that are building transformational digital tools to streamline clinical trials operations and data collection, inform study design, help oncology teams identify patients for research studies, and make clinical trials more widely available wherever patients receive their care. Flatiron conducts clinical trials in a nationwide network of community-based and academic practices that implement Flatiron technologies. The Research Oncology team works to ensure research quality and provide a patient-focused lens to development of new studies and digital products that re-envision the clinical trial landscape. This includes:

Providing clinical and scientific leadership to teams developing innovative approaches to running clinical research studies, such as novel study design and endpoint development
Serving as clinical lead for Flatiron’s portfolio of technology-enabled clinical trials, including:
Scoping and concept formulation in collaboration with life science partners
Study design and protocol development
Data and clinical oversight
Analytic guidance and data interpretation
Manuscript planning and execution
Data synthesis and Regulatory interactions
Leading analyses to evaluate the efficiency of novel clinical trial technology, solutions and operations
Representing Flatiron at meetings with life science partners, regulators and clinical investigators, and participating in speaking engagements and national committees as a thought leader in pragmatic clinical research
Providing clinical expertise for new services and products in development that provide value to the clinical research ecosystem
Contributing to the Clinical Research unit’s strategic development and growth, inclusive of team building and management
Collaborating with key cross-functional internal and external stakeholders

You’ll work closely with our Research Oncology, Regulatory, Clinical Operations, Clinical Data Management, Pharmacovigilance, Product, Research Sciences, Partnerships and Engineering teams.

Who You Are

You're a kind, passionate, creative, and collaborative problem-solver who values the opportunity to think beyond the way things are. You're a Medical Oncologist with experience in clinical research, who has worked at a bio-pharmaceutical/pharmaceutical company and/or CRO in support of an Oncology therapeutic area. You're excited by the prospect of innovating new ways to conduct clinical trials and rolling up your sleeves to tackle meaningful problems each and every day. You thrive in a fast-paced, multifunctional, team-based work environment at the leading edge of technology and medicine.

You have the appropriate experience required:
You have a Medical Degree (MD) and Oncology subspecialty training
You have 5-7+ years experience working in clinical research/clinical care/drug development, at least 5 of which are in the industry setting (e.g. clinical development, medical affairs, medical monitor)
You embrace the potential of new healthcare technology, and enjoy thinking about out-of-the box solutions to current trial pain points
You have a passion for ideating and creating novel trial designs with multiple collaborators
You have outstanding communication, writing and presentation skills
You have the ability to manage multiple projects simultaneously in a fast-paced environment
You have empathy for the challenges that oncologists and research staff face in the pursuit of clinical research
You are effective at driving collaboration, achieving results, influencing, and resolving conflicts across internal and external project teams
You can easily explain scientific and clinical concepts to a non-medical, highly sophisticated audience, and have a willingness to teach and learn
You are self-motivated, autonomous, and are able to prioritize

Extra Credit

You have formal experience with the FDA or other regulatory bodies
You have experience as a site PI
You have experience with clinical research digital technologies
You have experience with Flatiron’s real-world data and/or clinical research solutions

Where you’ll work

In this remote position, you have the freedom to choose your preferred work location while aligning your working hours with your team's. For further details on our hybrid work approach and remote work type, please visit the how we work website.

Life at Flatiron

At Flatiron Health, we offer a full range of benefits to support you and your loved ones so you can focus your working hours on improving cancer care and accelerating cancer research, and your non-working hours on everything else life has to offer:

Work/life autonomy via flexible work hours and flexible paid time off
Comprehensive compensation package
401(k) contribution to help you reach your retirement planning goals
Financial health resources including 1:1 financial advice
Mental well-being tools and services
Parental benefits and policies including family-building care and generous leave
Path to parenthood programs supporting fertility, adoption and surrogacy
Travel support for safe healthcare services

In addition to our robust benefit offerings, visit our Life at Flatiron page to learn how we support continuous learning and celebrate inclusion and belonging in the workplace.

Flatiron Health is proud to be an Equal Employment Opportunity employer.

We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

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