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Technical Writer level II
This is a 6 month renewable contract. Responsibilities: Will be required to perform statistical analysis of trending data. Must be able to summarize technical data for formal protocols. Candidate will write and review regulatory compliance related documentation. Will be required to perform data entry in global software systems. Will require excellent written and oral communication skills. Skills Must have excellent writing, mathematical and analytical skills. Must be proficient with Excel, Word, PowerPoint. Must be familiar...
Tags for this job: Pharmaceutical, Writer, Analysis, Data, Protocol, Technical, GMP, GLP
View Technical Writer level II Job - Fort Worth, TX 76134
Puerto Rico - Product Development Director
Our client is a leading technology company providing Electronic Health Records Management and claims processing solutions to the healthcare industry in Puerto Rico. The Product Development Director will be responsible to establish and lead the overall product strategy for company product suite to maximize revenue and profitability. Currently these provider-payer collaboration products consist of all tools to maximize financial efficiency and improve patient and member care for both payers and providers. Responsible for matrix-managing the product development process a...
Tags for this job: electronic, health, records, marketing, business development, EDI claims, electronic medical records
View Puerto Rico - Product Development Director Job - San Juan, PA 00918
Data Manager
Part time Data Manager position available with a pharmaceutical company available in Woburn, MA: 6 month contract that could be come full time after 6 months. Primary responsibility : Is to manage clinical trials through review, computerization, cleaning and auditing of clinical data and data bases in compliance with SOPS EDC and understanding of statistical concepts is a must •This position requires an individual with background in clinical data management, experience working with Electronic Data Capture (EDC) and database systems, and an understanding of Good C...
Tags for this job: data, EDC, CRO, pharamaceutical, statistical,
View Data Manager Job - Woburn, MA 01801
Clinical Trial Assistant
1 year contract for a Clinical Trial Assistant in Fort Worth, TX with a pharmaceutical company. Responsibilities: Daily tasks include coordinating printing and shipping of study documents, coordination and shipment of study supplies, entering information into clinical trial information systems, reviewing documents against archives. Skills Our ideal candidates have a background in clinical research, nursing, clinical study coordinator, or as an administrative assistant used to multi-tasking with good computer and oral and written communication skill...
Tags for this job: clinical, trials, coordinator, study documents, study supplies
View Clinical Trial Assistant Job - Fort Worth, TX 76134
Senior Clinical Project Manager
4 Senior Clinical Project Manager positions available in Cambridge, MA with a pharmaceutical company. These are 6 month renewable contracts starting ASAP. Experience - Demonstrated success being accountable for timelines and budget without direct authority over the people doing the work: ideally this would like like a project that was clearly successful in an organization that is not primarily project-based (so your resources are operational) - Clinical Development experience (either in operations or projects, at a sponsor or CRO) a big plus but not required So...
Tags for this job: project manager, trial manager, clinical trials, planning, MS Project, clinical development, sponsor, CRO, pharmaceutical, operations, pmp certification, sharepoint
View Senior Clinical Project Manager Job - Cambridge, MA 02139