Hands on team leadership opportunity to develop protein purification and characterization processes to support biologics manufacturing of Monoclonal Antibodies, Enzymes, Growth Factors, PEGylated Proteins and Cytokines derived from mammalian cell lines
*** Develop new purification procedures to be transferred and scale up to clinical and commercial manufacturing
*** Evaluate transferred processes, validate existing procedures, ensure viral validation, and train manufacturing team on new ...
Looking for a qualified SAS Programmer (home based)
Requirements include but are not limited to the following:
BA/BS degree in computer science, statistics, biostatistics, mathematics or related field. MA/MS degree is desirable
5+ years of programming and clinical research or related experience
Must have database management, SAS or PL/SQL programming experience
Or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills ...
$5000 Hiring Incentive for Qualified Candidates!
Covance is seeking Clinical Research Associates / CRA / Monitors with cardiovascular / coronary artery disease therapeutic experience for a special hypercholesterolaemia project.
Positions are home-based and urgently needed in the following locations: Raleigh, Dallas, Boston, Chicago, Minneapolis, NYC, Florida, and California.
Our Clinical Research Associates /CRAs / Monitors manage all aspects of site monitoring responsibilities for ...
This is a permanent position. Must have strong experience in Solid Tumor and/or Oncology.
Minimum of 2 years of Monitoring experience
Regional Travel: Regionalized, may on occassion be outside of region.
Job Key Duties and Responsibilities:
This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:
Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local ...
Lead teams focused on developing and optimizing the clinical development for novel oncology therapeutics through the use of predictive biomarkers and companion diagnostics.
*** Provide clinical and scientific input into Discovery Research and Early Development activities, including disease education, target identification, lead selection, preclinical pharmacology POC, nonclinical toxicology, biomarker strategy and IND enabling studies, to develop optimal translational medicine approaches ...
Title: Clinical Operations Lead--Work From Anywhere
Company: Pharmaceutical Company
Status: Full-time consulting engagement, 40 hours/week
Length: Long-term assignment: initial term 6 months
Our client is a multinational pharmaceutical company, headquartered in the US, whose goal is to ensure that people everywhere have access to innovative treatments and quality health care. Through working in partnership with everyone from patients to health care providers and managed care ...
Clinical Operations Leader
Responsible for coordinating the functional team members and their
activities across all geographies, liaising with project leadership and the sponsor to ensure that the Global Research Operations deliverables (timeline, quality, productivity) are met.
The ClinicalOperations Leader has overall accountability for the execution of the clinical operations strategy on the project. May act as Project Leader for projects involving a small number of services, where no Project ...
Seeking Medical Doctor with solid track record in clinical research and clinical trial design in person with: sound scientific and clinical judgment; knowledge of Good Clinical Practices (GCP), FDA regulations and guidelines; ability to effectively present ideas and document complex concepts in written and oral communication; experience providing expert support in a complex matrix environment; and ability to manage multiple projects.
*** Provide planning and oversight to clinical trials.
Job Title: Sr. Regulatory Medical Writer (Multiple Openings)
Location: East Coast Region – Home-based
Assignment Duration: Long-term W2 Contract
Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common ...
At Workforce Integration - Wi? - we know people are the key to successful organizations. So we have concentrated on getting people down to a Science. Ask us Wi?
Our client is seeking several Regional CRA’s to be based in the SouthEast, within 1 hour of a major airport. These are home based roles and critical to the company's continued success.
Role & Responsibility:
The selected incumbent will identify, select, initiate and close out appropriate investigational sites for ...
Mar 26 -
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