We are currently looking to hire Permanent Regional CRAs
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, ...
$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 ...
Radiant Research (radiantresearch.com) is comprised of 20 wholly-owned premier clinical research centers nationwide. Our clinical research centers provides a critical service to biopharmaceutical companies by recruiting study participants into clinical research, conducting the clinical research protocol and collecting the data necessary to support the safety and efficacy of the drug company's product to the FDA. Our client list includes every major pharmaceutical company and contract research ...
Seeking strategic expert and savvy diplomat to work closely with global pharma CEO in the analysis, selection and internal promotion of drug development strategies from evidence-based medicine to sustainable therapeutic solutions.
*** Support the analysis and selection of targets and entities for investigation and translation of non-clinical research results into clinical applications based on risk assessment and therapeutic area mission congruency.
*** Evaluate strategic agendas, policy and risk ...
As a key scientific leader create early clinical research strategies to drive the development of novel oncology therapeutics. Work with our clinics and laboratories to develop novel biomarkers, research tools and study designs derived from the safety, pharmacokinetic and pharmacodynamic data obtain in the early phase trials.
*** Determine the most efficient study designs, patient population and biomarkers to ensure the success of early clinical research
*** Conceptualize and implement ...
Seeking expertise in the identification and evaluation of gene expressed proteins or peptides acting as renal biomarkers to act as the primary contact and principal scientist and lead a small team in the design and development of mechanism of action studies for clinical trials and analyze and interpret data generated from MOA studies.
Additionally, shall lead collaborative efforts for in vitro cell based assays, stem cell differention, and biochemical assays design, development and data ...
Lead the development, implementation, and management of the GCP Quality program compliant with federal regulations (IRB and IEC) and company standards.
Candidate must possess at least 5 years experience in the following:
*** Developing and executing comprehensive annual audit plans for Clinical Trials.
*** Planning, coordinating, and conducting internal and external audits.
*** Overseeing and conducting GCP Training
*** Writing, reviewing, and updating Standard Operating Procedures
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 ...
PRIMARY JOB FUNCTION:
Independently executes and effectively communicates Clinical PK/PD development plans and strategies that achieve commercial goals and regulatory requirements. Generates new PK/PD study proposals. Proposes/contributes to PK/PD or regulatory advances, strengths, weaknesses, opportunities and threats, and responds with appropriate new strategies.
Consistently demonstrates an excellent record of accomplishment of Clinical Pharmacology and business objectives.
Serves as a lead ...
Data Analysis: Write SAS code for common statistical analyses. Understands and correctly uses validated SAS macros in the data analysis programs. Conducts thorough and detailed reviews of project documentation, program algorithms and analysis outputs. Interprets the analysis output clearly and effectively.
Identifies data analysis related issues and resolves promptly Study Preparation: Meets with CRA, R&D, Instrumentation scientists, department data collection programmers, and data entry to find ...
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 ...
We are in need of strong writers for a large CRO in the East Coast!
Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms
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 ...
My name is Candace and I represent The Fountain Group. We are a national staffing firm and are currently seeking a Clinical Research Associate for a prominent client of ours. This position is located in North Chicago, IL. Details for the positions are as follows:
Seeking an in-house CRA. Responsible for setting up and managing Clinical Research Committees, including project Steering Committee, Event Adjudication Committee, and Independent Data Monitoring Committee for large global ...
Mar 27 -
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