Medical Records Manager jobs in Delaware

Location: MA, RI, USA

Do you have expertise in, and passion for Medical Affairs in Oncology? AstraZeneca’s vision in Oncology is to help patients by redefining the cancer-treatment paradigm with the bold ambition to eliminate cancer as a cause of death. We are proud to work on ground breaking science with one of the broadest and deepest Oncology pipelines in the business. Help to advance our pipeline by applying expertise and accelerating our pathway to finding a cure.

We are seeking a Medical Science Liaison (MSL) to join us in our GI division! This role serves as the local medical voice of AZ in the disease area of interest and builds a local medical strategy to improve patient care and outcomes in their territory. The MSL is an established field-based professional with extensive scientific, clinical and therapeutic area expertise responsible for providing medical and scientific support for AstraZeneca's oncology marketed products, new indications for current products, and compounds in development.

***Territory is MA and RI ***

What you’ll do

• Act as the local medical leader responsible for developing a tailored strategy to meet the AZ USMA priorities in the disease area, as well as the local specificities and patient needs.
• Develop strong working relationships in different external business settings (e.g. academia, hospitals, managed markets, private practices)
• Lead scientific exchanges with oncologists and key members of the MDT
• Lead peer to peer scientific/medical interactions
• Gather insights on the treatment landscape, evolving healthcare environment and practice, barrier to optimal treatment and patient care or opportunities to improve outcomes of patients with cancer
• Discuss with KOLs data and educational gaps to ensure adequate use of our medicines and to inform our R&D strategy to address patient needs
• Stay current with scientific knowledge and attend relevant scientific meetings and conferences.
• Collaborate with Clin ops on Ph3 trials from feasibility to execution of trials

Minimum Qualifications

• Advanced degree required
• 2 years of MSL experience or relevant therapeutic area experience
• Demonstrated expertise in discussing scientific content and context to multiple audiences
• Strong understanding of clinical study design and protocols
• Basic understanding of the Healthcare system, clinical trial methodology, statistics and regulatory environment
• Excellent project management ability
• Ability to travel (40-60% by car and plane domestic)

Preferred Qualifications

• Doctorate strongly preferred in a health science or clinical field
• Advanced degree (i.e. Pharm D, MD/DO, PhD, PA or NP) in a relevant health science or clinical subject area

Why AstraZeneca?

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering ground breaking methods, and bringing unexpected teams together. Interested? Come and join our journey.

Are you ready to bring new insights and fresh thinking to the table? Brilliant! We have one seat available, and we hope it’s yours. Apply today.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.