MedFocus - North Carolina
Responsible for monitoring all types of clinical trials; assures adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. Core Responsibilities 1. Communication • Maintains timely and effective communication among team members and si...
MedFocus - Huntsville, AL
Responsible for conducting routine and non-routine analysis of raw materials, in progress and finished formulations according to standard operating procedures. Analytical chemist skill A MUST! Compiles data for documentation of test procedures and prepares reports. Calibrates a...
MedFocus - Swiftwater, PA
Job Title: Statistical Programmer with SAS programming skills in Swiftwater, PA. Duties: - The Statistical Programmer is responsible for providing significant programming support to the statisticians as part of the contribution towards the completion of statistical analyses (tabl...
MedFocus - Pennsylvania
Qualifications: • Must understand scientific process and have familiarity with medical and statistical concepts. • Must have strong analytic skills and ability to make data driven decisions. • Desire to work independently and ability to seek guidance as needed. • Must have good c...
MedFocus - Montville, NJ
Pharmaceutical Company looking for a contract Study Data Manager in Montville, NJ. Requirements: BA or equivalent preferred in Natural Sciences, Informatics or Medical Documentation Experience: Minimum 3 years as a Study Data Manger or comparable in projects and study teams. • Go...
MedFocus - New Jersey
• Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. • Assumes protocol level and some project management responsibility while supporting the Programming and...
MedFocus - Pennsylvania
Qualifications: • Master's degree preferred in epidemiology (or closely related discipline, such as biostatistics, biometry, public health or biological sciences) or Bachelor's degree plus three years related job experience, or equivalent experience. • Exposure to statistics and ...
Medical Information Specialist
MedFocus - Bothell, WA
*Medical Information Specialist needed to work in call center environment *Addressing inquiries that come in via drug information line. *Candidate must possess a solid year of working in a Medical Information Call Center environment for a pharmaceutical company *Oncology experien...
MedFocus - Thousand Oaks, CA
Description • Individual will partner with individuals within Clinical Data Management to provide operational support. • Duties include entry of data into vendor work order system, coordination and distribution of information, partner with vendor or internal functions to address ...
MedFocus - Massachusetts
Description: • Answering incoming calls from healthcare professionals and consumers. • Provide in-depth information and specific product and/or corporate knowledge to customers. • Resolution of customer issues may involve extensive analysis, research, and problem-solving. • Charg...
MedFocus - Thousand Oaks, CA
Basic Qualifications: • MD, 2+ years experience • Drug safety/drug development experience • Adverse Event Management Competencies: • Understand post-marketing safety, clinical trials and drug development • Clinical knowledge of therapeutic area patient populations and drug class ...
MedFocus - New Jersey
Qualifications: • Minimum two years Pharmaceutical Industry Regulatory experience. • Experience supporting Product Registration Data Management activities for global data in the Pharmaceutical Industry, specifically in the area of Aggregate Reporting. • Proven ability for data an...
MedFocus - Florham Park, NJ
Job Title: Global Program Allocation & Recruitment Manager in Florham Park, NJ Duties: Act as a global liaison between the clinical teams, the Regions and the CPOs to ensure optimal allocation and recruitment of studies, and adherence to resources and study timelines. Act as an e...
MedFocus - Illinois
Title: Clinical Studies Specialist - A in Northern Suburb of Chicago, IL. Description: - Requires attention to detail. - Administration experience a plus. - Required to file in Trial Master File for a minimum of 2 hours a day. - Sitting at a desk for at least 2 hours a day. Addit...
MedFocus - Massachusetts
• Work collaboratively with SMEs, project managers, and other technical writers to write, maintain and modify corporate standards, GOPs, Practices. • Ability to draft SOPs and Manufacturing Procedures • Slide deck from the CD Document Rewrite team explaining the new philosophies ...
MedFocus - New York
Primary Responsibilities: • Execution of local activities relevant to the management of safety data • Maintain local documentation as required by legislation (including archiving/tracking/retrieval) • Support the submission and distribution of reports and relevant tracking • Supp...
MedFocus - San Francisco, CA
Job Title: Regulatory Assistant in South San Francisco, CA. Duties: - QA final labeling and promotional materials and create high-quality, accurate submissions to FDA - Supports Promotional Review Committee (PRC) Chairs and PRC team members by reviewing and ensuring that content,...
MedFocus - Weston, MA
Title: Clinical Trial Manager in Weston, MA Description: It is important that this individual have Clinical Trial Manager experience, and preferably global experience and has worked with Asia Pacific. As a key member of the clinical operations team at Hemophilia, this individual ...
MedFocus - New Jersey
• Participate in ongoing comprehensive product/disease area training to serve as Medical Information expert within area of responsibility • Ability to communicate on professional level with physicians, nurses, pharmacists, and other professional staff when discussing products. • ...
MedFocus - Minneapolis, MN
POSITION DESCRIPTION: • Evaluate adverse events involving Neuromodulation products to determine MDR/ADR eligibility. • Report MDR/ADR eligible events to the FDA within the MDR/ADR regulatory requirements. Identify and initiate product event investigations to satisfy MDR/ADR requi...