Science Jobs in Durham, North Carolina

1000+ jobs

Data Science Program Manager ** NIH ** Research Triangle Park, NC Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Kelly Government Solutions offers administrative, IT, engineering, scientific, and healthcare professionals the opportunity to work with one of the ...

We are seeking an experienced Clinical Data Project Manager. This is a full time position available in our office in Research Triangle Park (NC).Primary Goals:? Responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality.? Responsible for the planning, organization, and coordination of Data Management & Systems, Statistics and Medi...

Planet Pharma is working with a client in Durham, NC to hire a Site ID Specialist. Please submit your resume or contact me directly at *****! Perform, manage and coordinate activities associated with identification of sites for projects or programs.RESPONSIBILITIESTake independent responsibility for assigned site identification projects.Assists Site ID lead on projects with inc...

Planet Pharma is working with a client to hire a Clinical Trial Associate for a 6 month contract that may extend. Please submit your resume here or contact me directly at *****. SUMMARY:May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.Primary Duties: The Clinical Trials Assistant (CTA) will sup...

• Develop, program, test and maintain clinical trial databases and data entry screens using SAS plus additional platforms. • Review computer validation/edit checks for in-house and outsourced studies• Develop, program, test and maintain computer validation/edit checks in SAS• Develop, program, test and maintain data review listings in SAS plus additional platforms. • Perform external data loads,...

Are you seeking a new medical writing job opportunity? Well look no further! We are looking for a Sr. Medical Writer with late phase experience to work from home. This is a contract to hire with good pay and benefits. Provides high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients. Provides...

Summary:Expedite contract negotiation and execution by acting as a resource and liaison for the Contracts and Grants group to streamline requests to law department and avoid duplication of efforts among Contract & Grants Analysts (CGAs) and CGA management.Act as main point of contact with legal department to resolve complex legal issues while ensuring compliance with company process and strategy a...

Position SummaryAssists in the management of the clinical monitoring process to ensure site adherence to applicable regulatory requirements, ICH/GCP Guidelines, company SOPs, and study protocols.Ensures coordination of an accelerated study start-up including pre-study visits, initiation, interim, and closeout activities associated with clinical trials to ensure timelines and metrics are met and ma...

Sr. Clinical SAS Programmer: Contribute to computer programming efforts for a clinical trial drug project and to provide programming support for clinical trial data reporting and regulatory submissions. Assumes protocol level and some project management responsibility while supporting the Programming and Statistics lead. Able to support multiple protocols independently and to contribute to integr...

We are seeking an experienced Clinical Data Project Manager. This is a full time position available in our office in Research Triangle Park (NC).Primary Goals:· Responsible for all data deliveries for assigned projects within time and budget with highest priority applied to data quality.· Responsible for the planning, organization, and coordination of Data Management & Systems, Statistics and Medi...

JOB DESCRIPTION:Responsible for the development and analysis of contractual relationships which includes but is not limited to drafting, negotiating, and finalizing contracts and grants related to clinical trials. Assists in and/or directs the development of scope of work and analysis of terms and conditions. Provides specialized support to trial managers and clinical group in the pricing, plannin...

Accountable to provide statistical input into the design of clinical studies, investigational plans, case report forms, database setup, edit checks, and clinical reports.Also responsible for providing consulting services to departments other than Clinical Affairs.Monitors own work performance and reports status to management.Coordinates technical decisions across organizational lines.Remains abrea...

Job Description: May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation. Primary Duties: The Clinical Trials Assistant (CTA) will support the clinical project team in the following areas: Accurately update and maintain clinical systems within project timelines. Prepare, handle, distribute, file, and archive clinica...

The Medical Science Liaison develops professional relationships with thought leaders and academic centers and translates those relationships into business and research opportunities, as well as providing timely, accurate, unbiased fair-and balanced product information to internal and external customers. The Medical Science Liaison disseminates technical and scientific presentations to critical sta...

PURPOSEIntegrated Processes and Technologies (IPT) provides cross-functional solutions integrating people, processes and technologies in order to make effective business decisions. Provide experienced, comprehensive and advanced technical expertise as part of a team to develop and maintain clinical systems to meet internal and external clients' needs.Plan and coordinate integrations and mapping of...

Job Title:Regulatory Project ManagerTo manage and maintain US applications (INDs, ODAs, and NDAs) for products in development and approved products according to ICH and FDA regulations Plans, coordinates and participates in writing, preparation, assembly, and maintenance of US applications to regulatory authorities Creates and manages submissions timelines and provides operational guidance and r...

Are you Nurse with a BSN looking for a new and exciting job opportunity? Well you should consider our Call Center Support Nurse job opportunity. Basic Qualifications: Bachelors degree with 3 years health sciences or related pharmaceutical experience. Must have demonstrated analytical, problem-solving, organizational, and interpersonal skills. Must have demonstrated oral/written communication skil...

*This position is work from home/remote.Clinical Programmer General Description: Plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provide technical expertise in conjunction with internal and external clients. Program, test, and document databases in accordance with programming standards and validation procedures. Program data...

Collaborates with various departments on the design, documentation and testing, and implementation of data associated with clinical studies. Develops systems for organizing data to analyze, identify, and report trends. Prepares reports of clinical trial studies for internal data validation and cross-study data validation. In some cases, evaluates and resolves issues regarding contents of reports. ...

OBJECTIVES: The Analytical Sciences Lead position within Vaccine Analytical Development will be responsible for: Establishing Takeda as a leader in vaccine analytical science through the application of processes, procedures and technologies in the development of best in class commercial laboratory testing strategies. Lead the validation and technical transfer of analytical techniques to externa...