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SCOPE Under general supervision of a physician and nurse (if applicable), is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials. Collaborates with physician in determining eligibility of patients for clinical trials. Provides education to staff and patients. Ensures site research quality by practicing in compliance with US Oncology Research
Posted Today
Pfizer
- Cumberland, RI / Washington, DC / Pearl River, NY / 55 more...
The Medical Outcomes Specialist (MOS) Special Projects will provide both consultative and direct customer and Field Based Medical (FBM) support and leadership to assess, develop, and implement complex, collaborative projects across the US. Examples include creating new paths within Pfizer to manage complex projects, leading complex studies and providing hands on market and customer consultation an
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of Position The Project Manager, GLP Lab is responsible for the effective management (planning, budgeting, forecasting, and scheduling) of all aspects of bioanalytical testing programs that supports MacroGenics' preclinical and clinical drug development studies. He/she will ensure adherence to GLP compliance and regulations, accurate budget management and resource forecasting, timely and flawless
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Covance
- Philadelphia, PA / Princeton, NJ / Washington, DC / 3 more...
Business Development Director Job Location(s) US PA Philadelphia | US NJ Princeton | US DC Washington | US NY New York | US CT Hartford | US MA Boston Job Number 2018 19525 Job Category Business Development/Sales Position Type Full Time Job Overview Responsible for selling highly scientific Translational Biomarker and Diagnostic Services to targeted accounts. Engages external and internal stakehol
Posted 1 day ago
Pfizer
- Pearl River, NY / Washington, DC / Las Vegas, NV / 54 more...
Leads a high performing team of specialized and experienced Oncology National Account Directors in a dynamic and evolving marketplace. National Accounts impact anywhere from 25% to 50% of the $5 billion and growing Oncology portfolio. Leads efforts to expertly engage national stakeholders in the marketplace and preserve Pfizer's position as the premier oral oncolytics manufacturer in the US Unders
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Sartorius Corporation
- Baltimore, MD / Raleigh, NC / Washington, DC / 1 more...
As one of the world's leading laboratory and pharmaceutical equipment providers, Sartorius is actively shaping dynamic, innovative and high growth markets. Founded in 1870, the company earned sales revenue of more than 1.4 billion euros in 2017. More than 7,500 people work at the Group's approximately 50 manufacturing and sales sites, serving customers around the globe. What you can look forward
Posted 2 days ago
Interfaces with various clinic providers to track patient appointments and verify eligibility. Reviews patient medical records; assists with patient identification, tracking, and enrollment. Obtains informed consent and provides education about the research study and procedures. Interviews patients regarding medical history and collects questionnaire data based on self report and medical record re
Posted 2 days ago
Pfizer
- Washington, DC / Pittsburgh, PA / New York, NY
The Oncology Field Medical Director (Onc FMD) is a field based medical colleague responsible for providing medical support in the assigned region focusing on the inline and peri launch oncology portfolio. The OncFMD role is to enhance medical communication between Pfizer and national, regional and local health care providers to support the safe and appropriate use of Pfizer Oncology medicines. The
Posted Today
Incumbent will serve in myriad capacities as a senior scientist/engineer, subject matter expert, principal investigator, system architect, technical lead, task lead or program manager focused on the research, development, and fielding of CBRNE signature collection, analysis or exploitation sensor or forensic science technologies, methods and services. Incumbent must work collaboratively with colle
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Faegre Baker Daniels' Health and Bioscience Consulting team, based in Washington, is seeking an advisor level consultant to join our nationally recognized Health Care and FDA practice. The ideal professional will support work across the team, including regulatory science work on patient focused drug development. He/she should also possess 3 plus years of experience in science and regulatory policy
Posted 1 day ago
Eastern Research Group, Inc. (ERG) seeks an entry level junior analyst to collect and analyze data on drug development programs for an analysis we are conducting for the Food and Drug Administration (FDA). Analyst will work with an experienced ERG project team onsite at FDA’s White Oak campus in Silver Spring, MD. Required Bachelor’s degree in the biological or physical sciences Excell
Posted 7 days ago
This position is responsible for internal execution of project work in the Drug Development Division under the direction of an assigned Project Manager and/or Study Director. Individuals in this role will work on studies that are complex and standalone or larger programs. A Senior Project Leader (SPL) will work closely with assigned project team members and related management for studies. SPL will
Posted 9 days ago
A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversityand where all colleagues are energized and engaged; and the abilit
Posted Today
By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that I agree with Takeda's Privacy Notice , Privacy Policy and Terms of Use. Job Description Are you looking for a patient focused, innovation driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as a Sales R
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Description of Responsibilities The primary responsibility of this individual is to review and inspect US and international clinical research and clinical trial sites engaged by USAMRIID, Division of Medicine. The secondary responsibility of this individual will be to assist with clinical research efforts at USAMRIID, including, but not limited to, management of a clinical sample repository. Tasks
Posted 6 days ago
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