Associate chapter administration program jobs in the Biotech, R&D, Science category and Healthcare Services industry

Job Description: The selected applicant will be responsible for clinical trial coordination and operation in the Community Clinical Oncology Program (CCOP) at Queens Hospital Center Cancer Center and Elmhurst Hospital Center. The selected applicant will manage a staff of researchers, initiating new multi-institutional protocols, encouraging patient participation in protocols and working with the o...
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Do you want to work in the fastest growing industry? Do you possess excellent interpersonal skills with the ability to multitask and service customers in an effective manner? [1]POSITION SUMMARY: [2]Monster has partnered with a leading pharmaceutical services company with a location in the Naperville, IL area on their search for Customer Service representatives for a new facility opening soon. The...
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Job Description: The Research Program Coordinator develops study protocols, designs management and statistical plans, analyzes data and prepares final reports from study. 1. Provides assistance and consultation on basic research or clinical trials methodologies and statistical analysis issues. 2. Participates in the primary analysis of evaluation datasets 3. Designs and implements research project...
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Description: Large, busy GI practice needs additional coordinator to support research program. Responsibilities: Coordinates and participates in clinical research studies conducted by principal investigator(s). Responsible for regulatory, budget and contracting for clinical trials, as well as organization of all study materials, subject recruiting and maintenance of subject study schedule and proc...
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Growing and well-respected biomedical (clinical, basic and applied) research firm has job opportunities at Wright Patterson Air Force Base. If you are passionate about research, and are looking for a firm that shares your passion, and provides competitive salaries with a strong benefits package, join the ClinicalRM team. We are currently seeking a Chief, Research Oversight & Compliance for the Day...
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Our hospital system is not just buildings, or remodeled nursing units, or the latest pieces of technology. Our hospital system is not defined by the awards we have earned or the number of patients we serve. What gives meaning to SCL Health System (SCLHS) is our people! It's our physicians, staff and volunteers who display their commitment to our mission and our values in exceptional ways every day...
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Job Description Our mission is to provide the highest quality health care. Be the leading source of research and discovery; educate the next generation of leaders in child health. So if improving a child's life, a care provider's expertise, a community's well-being and the world's knowledge sounds like a rewarding day's work to you, keep reading. Please apply to the link and mentioned how you foun...
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Subject Matter Expert (SME) for Blood Products and Regenerative Medicine this is a 5 year commitment, you may not need to relocate on a perm basis We have a long term contract opportunity available for one of our U.S. Federal Government clients located in Washington, DC. A Regulatory & Quality Affairs Analyst is needed to provide advice, program management (PM) support, and mentorship to a governm...
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A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewarding employers in our field. A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancemen...
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The Senior Clinical Research Specialist position is responsible for overseeing and managing the overall conduct and operational activities of one or more multi-center clinical research studies. Position is responsible for managing all aspects of the study including internal, site and data management. Qualified candidates should 5 years experience directly supporting clinical trial as a Clinical Re...
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Master's degree is preferred Certification Required 3-5 years experience is required Experience is required Supervisory experience is required Reporting to the Manager of Microbiology, this position is responsible for direct supervision of the staff within the Microbiology Section of the department. Keeps the Manager informed of all necessary information. In collaboration with the Manager, the Sup...
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Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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Catalent Pharma Solutions (a Blackstone Group company) is a leading Drug Development, Advanced Delivery Technology and Supply partner to the global pharmaceutical industry. A Fortune 1000 company, with over 20 locations on 5 continents, we partner with 90 out of the top 100 pharmaceutical companies and 44 of the top 50 biotech firms, as well as thousands of small innovator companies. The position ...
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Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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Description Description Assist physicians inpresenting, consenting, and managing the record of patients, consented and enrolled to clinical trials, assuring compliance with Federal regulations regarding the conduct of clinical trials. These services further the vision of Desert Regional Medical Center to create unique environments, where patients, their families, doctors and staffcome togheter to ...
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Clinical Research Associate This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Working within a highly qualified team our Clinical Research Associates (CRA’s) identify, select, initiate and close-out investigational sites for clinical studi...
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. Exciting direct hire opportunity for a Full Time Clinical Research Associate in Pleasanton, CA! Responsibilities include: Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects; May co-ordinate the activities of relevant colleagues within the Company and investigators to ensure compliance with the overall scie...
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CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Lab Associate Cerritos, CA; Irvine, CA Full-Time $35,000 - $45,000 Posted 5/24/2013 Anna Thomas is recruiting for this position. Email your resume to Anna Apply Job Details If you are a Lab Associate with experience, please read on! If you are a Lab Associate with strong cell culture experience, this is an excellen...
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Abbott & Associates Professional Placement A unique, quality driven organization specializing in delivering professional placement and in candidate diversity Abbott & Associates is looking for a Cancer Research Assistant for a client company who prides themselves on delivering quality health care. In this position as the Clinical Research Associate you will coordinate and maintain a diverse set of...
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There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we have an opportunity available for a Project Associate at our Valencia, CA office. Support Pr...
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JOB TITLE – Home-Based Clinical Research Associate GENERAL SUMMARY OF DUTIES – Perform routine site monitoring visits, participate in site selection, site initiation and study closure activities to ensure that the clinical trial is being conducted according to the approved protocol, amendments and in compliance with Good Clinical Practice (GCP), company SOPs, and all applicable regulatory requirem...
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Job Description: Under moderate supervision, conducts routine and standardized experiments using advanced techniques specific to the research project. Analyzes and assists in interpreting moderately complex results. Duties and Responsibilities: 1. Conducts routine and standardized experiments using advanced research techniques specific to subject matter of the research project. 2. Analyzes and ass...
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Description: Major Responsibilities: Plan, organize and manage data collection aspects of assigned chart abstraction or survey research activities Lead and manage the efforts and performance of all project consultants and vendors to execute project activities according to project milestones including contracting, invoicing and data management Act as a primary liaison for study team members and thi...
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Supports Study Managers and other appropriate staff in coordinating and overseeing all aspects necessary for clinical study progression according to the study protocol and Standard Operating Procedures (SOP’s). Responsibilities: · Support the Study Manager with completion and QC of subject charts, study documentation and tables. · Assist with study preparation by attending initiation meetings and ...
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Requirements: BS life sciences 4+ years of experience working in clinical operations in compliance with GCP Broad range of experience with various stages of clinical trials, from study start up through database lock Experience working on oncology trials or autoimmune trials required Experience being direct point of contact at sponsor for CRO for study required Appropriate experience to perform ong...
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