55 Opportunities

Sign in to chat with employers - save searches and jobs!  Sign up / Login

Posted 6 days ago

Work ActivitiesDocumenting/Recording InformationPerforming Administrative ActivitiesEstablishing and Maintaining Interpersonal RelationshipsInteracting With ComputersProcessing InformationTHE DUTIES ARE:* Keep records of materials filed or removed, using log-books or computers.* Add new material to file records, and create new records as necessary...

Posted 6 days ago

Work ActivitiesDocumenting/Recording InformationPerforming Administrative ActivitiesEstablishing and Maintaining Interpersonal RelationshipsInteracting With ComputersProcessing InformationTHE DUTIES ARE:* Keep records of materials filed or removed, using log-books or computers.* Add new material to file records, and create new records as necessary...

Posted 2 days ago

Seeking individual to manage bioanalytical projects for early phase clinical trials conducted on behalf of major pharmaceutical organizations in one of the industry's leading contract research organizations known for the quality of their work, technical ability . Shall: *** Participate in client meetings and act as liaison to project team inclu..

Posted 2 days ago

Seeking experienced immunoassay development scientist with direct experience in a CRO environment to join a talented team of experts working on protein, peptide, and antibody analysis supporting clinical trials. Requires: *** Experience in a CRO environment - or similar capacity with multiple concurrent projects and strict deadlines. *** Expe..

Posted 1 day ago

Join a leading organization with customers including the largest pharmaceutical companies with promising new drugs in preclinical research and early clinical trial phases. Seeking experienced project manager or project lead with specific background in bioanalytical method development who can: *** Oversee work of junior scientists and coordinate..

Posted 1 day ago

Seeking experienced scientist to develop, validate, and execute bioanalytical methods for the qualitative and quantitative analysis of new protein, peptide, and antibody (mAb) entities in biological matrices (tissues, plasma, etc.). Shall: *** Design and execute experiements to quantitatively measure molecular entities using ELISA, Gyros, Meso ..

Posted 1 day ago

Seeking experienced Bioanalytical Project Manager to develop and validate biomarker, cell-based, immunogenicity, immunoassays and enzymatic assays to support preclinical, clinical, and product release studies. Requires expertise in a CRO environment with multiple concurrent projects and non-flexible deadlines. Qualifications: *** Hands-on exp..

Posted 1 day ago

Seeking Senior Scientist with PhD and direct industry experience supporting clinical trials in a CRO environment, or similar, who has hands-on expertise with immunoassay method development, validation, and execution supporting PK-PD (pharmacokinetic-pharmacodynamic) modeling, immunogenicity studies, or similar for drug discovery. Shall: *** Lea..

Posted 9 days ago

Seeking expert Medical Writer with specific Regulatory expertise in Phase I and II clinical trials to join a growing team supporting new Phase II trials and closing Phase I trials for novel vaccines. Shall: *** Compile, write, edit, and review regulatory documents and responses to regulatory authorities (FDA, Notified Bodies, etc.), including C..

Posted 9 days ago

Seeking scientific Medical Writer with experience in drug, vaccine, or device clinical trials with a focus on Phase I and II studies. Required: *** 5 years medical writing experience with specific expertise developing, writing, editing, and updating documents including: Investigator's Brochures (IBs), Clinical Study Reports (CSRs), Nonclinical..

Posted 9 days ago

Seeking individual with experience in regulatory submission writing for closed and closing Phase I and II clinical trials; experience with clinical trials for therapeutic drugs, vaccines, medical devices considered. Requires knowledge of, and direct experience with: *** Regulations governing clinical trial documentation. *** CFR 21 parts 11, ..

Posted 9 days ago

Seeking experienced Medical Writer with three years of early phase I through II clinical trials experience in a pharmaceutical company, contract research organization, or vaccine development company. Shall develop, write, edit, format, and submit the following documents to the clinical and regulatory team: clinical study reports, manuscripts, eff..

Posted 9 days ago

Seeking experienced Medical Writer well versed in the regulatory requirements governing clinical trial documentation, reporting, and FDA submission. Shall: *** Draft, edit, and submit clinical and regulatory documents including clinical abstracts, posters, manuscripts, safety reports for closed and closing Phase I and II clinical trials. *** ..

Posted 9 days ago

Seeking experienced Medical Writer with specific expertise in writing clinical documentation required for Phase I through II vaccine trials including study protocols, informed consent forms, safety reports, abstracts, and other manuscripts. Why should you join a leading organization with multiple approved products and several promising vaccines i..

Posted 6 days ago

Its a powerful feeling, to belong. Its finishing each others thoughts. Laughing at the same jokes. Its that moment you feel truly and completely yourself. Its working with people who treat you like family. At Marriott we know that when you feel at home, youll make our guests feel at home. If this sounds like the place for you, join us. The Courtyar..

Posted 10 days ago

Position title: Claims Examiner Length of contract: Temp to HireLocation: Quincy, ILPay Rate: 11.77 to 12.77 depending on experienceJob Description:BASIC FUNCTION:Under supervision, this position is responsible for processing complex paper and electronically submitted claims requiring further investigation and coding; resolving pended claims and pr..

Posted 30 days ago

These are some of the top opportunities available with a variety of Contract Research Organizations, Biotech and Pharmaceutical companies in Massachusetts. Our clients are growing their assay development teams for the New Year and need individuals with industry experience in the following areas: Sr Scientist - In Vitro Diagnostic (IVD) Assay De..

Posted 30 days ago

Here are the top opportunities available for Regulatory Affairs and Regulatory Operations experts to interview for in the New Year. Our clients are looking to hire candidates to add to their teams in 2017. Regulatory Affairs eCTD Submissions Specialist - $120k - Mansfield, MA Requires experience leading submission of INDs, NDAs, ANDAs, BLAs..

Posted 30 days ago

Our Company specializes in placing scientists into positions with leading companies focused on vaccine discovery and development. Our Massachusetts based clients are looking to get a head start on 2017 and requested we begin interviewing candidates for the most critical positions. Sr Scientist - Downstream Process Development - to $95k - Cambri..

Posted 30 days ago

Our clients, ranging from Contract Research Organizations to Biotech and Pharmaceutical companies are growing their assay development teams for the New Year and need individuals with industry experience in the following areas: Assay Development and Validation Scientist - to $130,000 - San Diego, CA Requires 5 years industry experience deve..
Show more