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The Professional Healthcare Representative may have a variety of responsibilities, such as the responsibility for sales targets and physician relationships within a specific geography. The Professional Healthcare Representative must demonstrate a strong understanding of necessary disease states and possess a solid ability to communicate necessary technical, scientific, and product and disease mana
Full Time / Bachelor's Degree Required
Posted Today
Develop and Lead PHT strategy for PBM program development (20%) Identify and define viable PHT/MSH roles that are marketable and profitable for PHT/MSH in the areas of PBM and UHC. Identify and evaluate partnering options and negotiate agreements with selected partners. Work with PHT Senior Director for New Business to develop a written 2 3 year business strategy with measurable indicators and gai
Full Time
Posted 1 day ago
Assists pharmacist(s) in all areas of pharmacy operations, including prescription preparation, sales transactions, customer service, and purchasing and inventory maintenance. Qualifications EDUCATION High school graduation or equivalent. EXPERIENCE 6 months pharmacy technician experience in a retail setting or equivalent training. LICENSE/CERT/REG Must have successfully completed the pharmacy tech
Full Time / High School or Equivalent Required
Posted Today
scientific and clinical data collection and analysis
Responsibilities Primary responsibilities include scientific and clinical data collection and analysis (predictive and prescriptive); planning and support of scientific meetings/teleconferences; stakeholder/client communication management with various collaborative groups. Perfect opportunity for a recent college grad. Requirements Qualifications include a BS degree; life science degree would be a
Full Time / Bachelor's Degree Required
Posted 4 days ago
Knowledge of GCP and ICH guidelines preferred
Perform various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation, preparation of IND safety reports for submission to the FDA, safety document or data analysis, and clinical trial site support. Collecting accurate information from the site as required per the project and also responding to site queries. Review IND Annual Re
Full Time / Doctorate Required
Posted 4 days ago
U.S. medical license required/Infectious disease and/or oncology subspecialty highly preferred
Responsibilities The Safety and Pharmacovigilance Specialist will perform various tasks in support of clinical research including adverse event analysis and processing, serious adverse event reconciliation, preparation of IND safety reports for submission to the FDA, safety document or data analysis, and clinical trial site support. Requirements M.D. from a U.S. accredited institution with active
Full Time / Doctorate Required
Posted 4 days ago
Posting Title Sr. BioAnalytical Research Associate Trainer Requisition ID 67596BR Job Category Biotechnology/Pharmaceutical Locations United States Chantilly, VA Shift 1 Job Posting Covance is seeking a Senior Research Associate Trainer to join their large molecule BioAnalysis team in Chantilly, VA. This is an excellent opportunity for someone with a strong analytical background with experience tr
Full Time / Bachelor's Degree Required
Posted 4 days ago
pharmaceutical, biologics, and/or diagnostic experience
Responsibilities This position will manage and process SAEs; assist in the preparation of reports; generate specified data reports from the database; process and review investigator safety reports and notifications for non IND adverse event reports; process and review safety narratives for IND and non IND Adverse Event cases as required; maintain electronic files for the department; and query SAE
Full Time / Bachelor's Degree Required
Posted 4 days ago
Pfizer - 
Silver Spring, MD / Peapack, NJ / Collegeville, PA / 4 more...
The GCMC Manager is responsible for the development of regulatory strategies, submissions and compliance activities for medical device related development programs and commercial products supporting Pfizer's Consumer Health Business Unit. The manager will Generate and drive strategic and operational global regulatory CMC direction and documentation for assigned projects/products covering initial r
Full Time / Bachelor's Degree Required
Posted Today
Participate in the review, planning and implementation of clinical trials. This will include the evaluation of study design, feasibility, pharmaceutical regulatory requirements, and identifying solutions for pharmaceutical and logistical problems that may impede the conduct of a study. Develop the text for the study product section of the protocols in cooperation with members of the protocol team
Full Time / Bachelor's Degree Required
Posted Today
Field Support Technician Baltimore/DC United States, Maryland, Baltimore As a Field Support Technician you will serve as a resource for the technical maintenance and installation of Roche products for assigned product lines. You will perform on site preventative maintenance, installation, and technical updates (TSB's) on company product(s). You will diagnose mechanical, hardware, software and sy
Full Time / High School or Equivalent Required
Posted 2 days ago
Level Undisclosed Salary Range Undisclosed Job Location USA VA Travel Percentage Undisclosed Position Type Internship Job Shift Undisclosed Education Level Undisclosed Job Category Undisclosed Description CRDF Global's biosecurity practice area is seeking an intern to sup
Full Time / Bachelor's Degree Required
Posted 4 days ago
Good Clinical Practices and/or experience working in an FDA-regulated environment is desirable
Responsibilities This position is part of a team supporting government sponsored clinical trials. The key responsibilities include Draft pre IND packages, FDA correspondence, and other regulatory submissions in support of active and planned investigational applications (INDs, NDAs, BLAs, IDEs, etc.) Prepare regulatory submissions using electronic submission publishing software, to be submitted to
Full Time / Bachelor's Degree Required
Posted 4 days ago
Job Description Title Regulatory Affairs Specialist Department Regulatory Location Columbia, MD (potential for Lafayette, IN) Type Full time Job Summary The Regulatory Affairs Specialist assists the Head of Regulatory Affairs with U.S. and international activities relating to strategies for regulatory submissions, clearances, approvals, licenses, and registrations. Principal Responsibilities Assi
Full Time / Bachelor's Degree Required
Posted 5 days ago
The key focus of the Professional Healthcare Representative (PHR) is to increase the level of Pfizer Vaccines product sales within assigned portfolio and geography. This is accomplished through regular on going contact with providers and by building solid working relationships with providers that ensure continuing access that enables the use of effective direct selling techniques. The PHR is respo
Full Time / Bachelor's Degree Required
Posted Today
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