Clinical assistant rater training jobs in the Biotech, R&D, Science category in Arden, Delaware

Job Description – Associate Director – CNS Rater Reliability Services ePharmaSolutions (ePS) is an industry leading global clinical services and technology solutions provider that supports the top pharmaceutical, biopharmaceutical and clinical research companies in the world. Our core services focus on improving site selection, study training, rater reliability, and patient recruitment and retenti...
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Job Description – Clinician, Scientific Affairs and Clinical Assessment LOCATION: Philadelphia Area SUPERVISOR: Director, Scientific Affairs and Clinical Assessment SUMMARY: TheClinicianis responsible for all aspects of assigned projects that include clinical assessment, training development and data review for Worldwide Clinical Trials, Inc. (WCT). The Clinicianworks under the direction of the Di...
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Job Description – Clinical Manager, Scientific Affairs and Clinical Assessment LOCATION: Philadelphia Area SUPERVISOR: Director, Scientific Affairs and Clinical Assessment SUMMARY: TheClinical Manageris responsible for all aspects of assigned projects that include clinical assessment, training development and certification for Worldwide Clinical Trials, Inc. (WCT). The Clinical Managerworks under ...
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Drexel is ranked one of the best national universities in the category of Best National Universities in “America’s Best Colleges” for 2012 by U.S. News & World Report for the eighth consecutive year and in the top 100 for the fourth straight time. Drexel also ranked sixth among national universities in the U.S. News list of "Up-and-Comers," those schools most often cited by university administrato...
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Minimum Requirements • University Degree or equivalent • A specialist knowledge of contract and procurement management, with specific reference to the pharmaceutical/health care industry. • A demonstrated knowledge of contracting/commercial processes preferably from the CRO industry • A good understanding of procurement and project management tools and processes. • Comprehensive knowledge of clini...
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Responsibilities: § Lead and support the scope and commercial aspects of the external delivery solution (Procurement) for Drug Projects, managing a portfolio of external partners and providers. § Drive the contract management process as defined in the Clinical Procurement Process Framework and facilitate training to the project/delivery teams. § Lead regional cross-functional teams and participate...
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Johnson & Johnson companies are equal opportunity employers. Principal Clinical Research Scientist (West Chester, PA)-3377130307 Description DePuy Synthes, a member of the Johnson & Johnson Family of Companies is recruiting for a Principal Clinical Research Scientist. This position is located in West Chester, PA. DePuy Synthes Companies of Johnson & Johnson is the largest, most innovative and comp...
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If you’re interested in working for a Leading, Mid-Size Contract Research Organization (CRO) that has a massive global reach, then look no further, because Pharm-Olam International offers all of that and more! We are a company that strives to deliver cost-effective, quick-to-market clinical services in today’s emerging marketplace. Pharm-Olam International (POI) has one of the largest global footp...
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Solution Specialist, Clinical Informatics Our life sciences knowledge and information are essential for drug companies to discover new drugs and get them to market faster, for researchers to find relevant papers and know what’s newly published in their subject, and for businesses to optimize their intellectual property and find competitive intelligence. Main Purpose for a job: We are looking for a...
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ePharmaSolutions is an industry leading clinical trial technology & niche services provider to the life sciences industry. Our award winning eClinical solutions are used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies and CROs in the world. We are again expanding our clinical operations department to include several Clinical Project Coordinators w...
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ePharmaSolutions is an industry leading eClinical solutions & niche services provider to the pharmaceutical industry. Our award winning Clinical Trial Portal is used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies in the world. Our company is experiencing tremendous growth due to accelerated adoption of our eClinical solutions and niche clinical s...
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ePharmaSolutions is an industry leading clinical trial technology & niche services provider to the life sciences industry. Our award winning eClinical solutions are used by more than 300,000 clinical researchers in 130 countries for the top 20 pharmaceutical companies and CROs in the world. We are again expanding our clinical operations department to include several Senior Clinical Project Manager...
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The Wistar Institute, located adjacent to the University of Pennsylvania’s campus in Philadelphia, was founded in 1892 as the first institution of its kind devoted to medical research and training and is recognized today as an international leader in basic biomedical research, most especially in areas related to cancer. We currently have multiple openings for Research Assistants in the in both sci...
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Yoh has a contract opportunity for a Clinical Submissions Specialist to join our client in Wilmington, DE. Job Responsibilities: - Effectively communicate submission format requirements to the submission team. - Collect necessary information and requirements from the submission team. - Compile and publish regulatory submissions in accordance with current standards and processes using agreed upon t...
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Job description: Sr. Statistician to Sr. Manager, Biostatistics - This position is responsible for providing statistical support to drug development programs. Job Responsibilities: • Provide statistical input to study protocols • Develop statistical analysis plan • Monitor internal and CRO project activities including timelines, deliverables and availability of resources • Interpret study results ...
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Develop and enhance applications based on specifications. Codes and tests according to design specifications. Skilled in coding, testing, and implementing configuration changes to software applications to meet both functional and technical requirements. Unit test applications and develops system and user documentation.Some responsibility over other developers with less experience. Minimum of a Bac...
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MUST HAVE: 1.) Prior experience acting as a team lead/project lead within Clinical Data Management 2.) Inform 3.) Oncology 4.) RN, or BS 5.) 10+ years of CDM exp Description: -Assisting with clinical data management for clinical trials in a group that is very loosely structured; must be able to work independently, utilize critical thinking and judgement, and be able to work with little direction -...
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We are seeking a detail-oriented Contracts Specialist to negotiate and administer clinical research and related agreements such as confidentiality, data and vendor agreements. Main Job Tasks and Responsibilities Extensive interaction with internal and external legal counsel, contracts personnel, medical staff, project managers, and clinical research associates Job Qualifications Excellent organiza...
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Lab Assistant At NextGen, we don’t just hire people, we hire up, that is, the best and the brightest, matching talent with great companies across the United States. Ours is a process of discovery, learning everything we can about our candidates and our clients, in order to achieve the best possible match. We know that behind every placement, there are real people looking for an opportunity and the...
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The Senior Biostatistician / Therapeutic Area Lead will be responsible for coordinating with the project management in meeting the timeline and defining/ capturing the metrics for monitoring and maintaining the quality and productivity · Good verbal and written communication skills coupled with good organizational skills · Leadership skills, people management skills & ability to guide and motivate...
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Responsibilities: § Lead deliver committed components of clinical studies according to agreed resources, budget and timelines § Comply with Procedural Documents, international guidelines such as ICH-GCP as well as relevant local regulations § Ensure sites are identified, site qualifications performed, set up, initiated, monitored, closed and documentation archived Experience: § 5+ years pharmaceut...
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Senior Clinical Statistical Programmer Description: Minimum of a Bachelors degree, Masters Preferred Minimum 8 years SAS programming experience in the pharmaceutical, biotechnology, and/or contract research organization industries The Clinical SAS Programmer creates SAS programs in support of sponsors clinical trials according to SOPs and guidelines. This programmer will create, document, validate...
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Basic Qualifications: 1. Minimum 1 years in pharma working on clinical trials 2. Minimum of a Masters in statistics 3. Minimum 1 years experience using SAS The Statistician will be responsible for the following: " Participate in the design and review of clinical protocols and case report forms including preparation of statistical sections, sample size calculations, randomization, and study design ...
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Senior Manager Clinical Supplies - New Jersey My client is a well-funded global biotech company with multiple programs in late stage clinical trials. They were recently awarded over $50 Million in funding. They have retained Klein Hersh to bring on a Senior Manager Clinical Supplies. This is a key role within the organization, reporting into the Vice President. Additionally, the Senior Manager Cli...
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The Sr. Clinical Research Associate - Level I, Site Start-up performs and coordinates site evaluation visits in accordance with ICH Good Clinical Practices and FDA guidelines and global Standard Operating Procedures to ensure the selection of appropriately qualified sites of investigational products and/or medical devices. Works in conjunction with the Clinical Submissions Specialist(s) and Clinic...
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