Clinical/Medical Scientist (Medical Monitoring) - Oncology - Breast

## Join Syneos Health as a Clinical/Medical Scientist in Oncology

At Syneos Health, we are a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a functional service provider partnership or a full-service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need. This is a fully remote position.

### What You’ll Do

You will work closely with our Medical Director to develop medical plans including the Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan. This involves engaging with outside experts, consultants, and advisors to coordinate the medical and scientific input needed to prepare those plans. You’ll perform regular and ad-hoc medical review of data listings and data visualization, analyzing the data to identify risks and patterns, and supporting documentation of medical reviews. Proactively identifying and resolving medical data review issues as they arise is key. You will author medical data queries, review responses, and approve query closure in collaboration with the Medical Director. You may also assist the Medical Director in patient profiles review, scientific review of other study-level data, protocol deviation review, and creation of Medical Review Summary reports as needed. Partnering with Medical Directors for medical data review and safety review meetings, including slide preparation, is also part of the role.

You’ll manage project scope of work, objectives, and quality of deliverables to ensure project milestones and timelines are met, serving as the primary interface between internal teams, customers, and vendors in the areas of medical data review and eligibility review. Working with study team members across Clinical Operations, Data Management, Drug Safety and Pharmacovigilance, and Project Management, you’ll set up and lead meetings as appropriate to identify risks related to data integrity and subject safety. Escalating ongoing and newly developed study concerns—such as at-risk deliverables and out-of-scope tasks—to project leads in a timely manner is expected. You’ll attend and present at Trusted Process meetings and may participate in internal and external audits. This role requires you to acquire a basic understanding of ongoing protocol designs, disease-related terminology, and pathology. Adherence to all data privacy guidelines, ICH, GCPs, enterprise policies, SOPs, work instructions, and project plans is mandatory, and you’ll adhere to customer policies as required in project plans. You may also manage a limited number of direct reports and participate in interviews.

### Our Culture & Benefits

We believe in providing an environment where our people can thrive, develop, and advance. We reward and recognize our people with valuable benefits and a quality-of-life balance. Benefits for this position may include a company car or car allowance, health benefits (Medical, Dental, Vision), a company match 401k, eligibility to participate in an Employee Stock Purchase Plan, eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary. Syneos complies with all applicable federal, state, and municipal paid sick time requirements. The base salary range for this role is $67,700.00 - $115,100.00, and actual salary will vary based on factors such as qualifications, skills, competencies, and proficiency. Over the past 5 years, we have worked with 94% of all novel FDA approved drugs, 95% of EMA authorized products, and over 200 studies across 73,000 sites and over 675,000 trial patients. You’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment.

---

_This job was found on [bandana.com](https://www.bandana.com/?utm_source=jd_attribution&utm_medium=repost)_