9 jobs found

Medical Billing Specialist-Behavioral Health Billing Specialist for a Mental Health and Substance Abuse Treatment, non-profit Provider in the Cambridge-Somerville Area. Terrific opportunity for advancement in the Medical billing field for someone with some experience in the behavioral healthcare area. We will provide specific training. General responsibilities include interaction with patients, staff, and insurance companies and outside regulators as well as performing all billing functions. Candidate must be detailed oriented and be familiar with electronic billing systems. Interaction with accounting packages a plus. Other accounting responsibilities as needed. About North Charles Mental Health Research and Training Foundation, Inc. North Charles is a non-profit provider of mental health and addiction treatment services. For over 42 years, North Charles has provided accessible, high-quality, and affordable treatment services for thousands of individuals in the Cambridge,...

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference.If this is your profile, we want to hear from you. The Associate Director (AD), Alzheimer's disease MSLs is responsible for the leadership, direction and management of the MSLs within their region. This includes providing overall guidance and direction to the MSLs to gain an understanding of the scientific landscape from KOLs/HCPs and communicate the information to key...

The Role: The Associate Director of Medical Writing is an incredible opportunity to work under the direct mentorship of our Director or Senior Director of Medical Writing. The chosen candidate will not just be a part of Moderna's medical writing team but will lead the charge in delivering high-quality clinical and regulatory writing. From masterminding the planning and coordination to spearheading the delivery of final drafts, your role of Associate Director of Medical Writing will be pivotal. They will be the linchpin connecting the clinical development team, understanding and translating how their work shapes the broader objectives of Moderna's clinical development program. This is not just a job, it's an opportunity to drive change and make a difference in the world of biotechnology. Here's What You'll Do: Functional Knowledge: Possess specialized depth and breadth of knowledge for managing medical writing and regulatory writing within a clinical development program....

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Job Title: Associate Director, Global Medical Quality Location: Remote About the role: As Associate Director, Global Medical Quality, you will be empowered to lead Quality Assurance activities for assigned post-marketing research activities performed by Takeda including the management of audits, quality issues and their investigations, and inspections. We ask that you have an in-depth of understanding and experience in both GCP and GVP compliance to conduct responsibilities independently. You will report to the Head, Global Medical Quality Pharmacovigilance and Medical Quality. How you will contribute: * The research...

Job Details By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use . I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description About the role: At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on three therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Global Medical Communications, GMA Congress Excellence where you will be responsible to support the development, operationalization, and execution of Takeda GMA's scientific and medical congress strategy. This role will...

Associate Director, Medical Writing page is loaded Associate Director, Medical Writing Apply locations Cambridge, Massachusetts Clinical Development time type Full time posted on Posted 2 Days Ago job requisition id R14688 The Role: The Associate Director of Medical Writing is an incredible opportunity to work under the direct mentorship of our Director or Senior Director of Medical Writing. The chosen candidate will not just be a part of Moderna’s medical writing team but will lead the charge in delivering high-quality clinical and regulatory writing. From masterminding the planning and coordination to spearheading the delivery of final drafts, your role of Associate Director of Medical Writing will be pivotal. They will be the linchpin connecting the clinical development team, understanding and translating how their work shapes the broader objectives of Moderna’s clinical development program. This is not just a job, it's an...

Work_Category - hybrid Description The Associate Director, Statistical Programming Medical Affairs is responsible for statistical programming activities in support of Medical Affairs including technical and project leadership, overseeing the quality and timely delivery of all statistical programming.He/she ensures the team develops, maintains, validates and runs quality SAS programs that access, visualize, analyze, and report data in accordance with statistical analysis plans, ICH guidelines, and applicable regulatory requirements. Summary of Key Responsibilities * Provides technical and/or operational leadership in the delivery of high quality and timely statistical programming for publications, abstracts, and other Medical Affairs requests * Works closely with Biostatistics to implement statistical analysis of clinical trial data, working closely on the development and validation of analysis dataset specifications and datasets, and TLFs for analyses to support...

Janssen Research and Development, L.L.C., a member of Johnson and Johnson's Family of Companies, is recruiting for an Associate Director, Translational Clinical Medical Lead (TCML) , Immunology Translational Sciences and Medicine (TSM) to be located in Cambridge, MA, Spring House, PA or La Jolla, CA. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit http://www.JanssenRnD.com for more information. We are Janssen. Our mission drives us. Our patients inspire us. We...

At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Global Medical Communications, GMA Congress Excellence where you will be responsible to support the development, operationalization, and execution of Takeda GMA’s scientific and medical congress strategy. This role will serve as the champion to create a roadmap and process for Medical Congress presence and engagement and requires a person who can collaborate cross-functionally to create an industry-leading operational framework and work independently in a fast-paced environment. You will also be Accountable for supporting strategic plans with business partners, supplier management and assurance of legal,...