Provide front line medical support to subjects. Intervene and document when adverse events occur and verify follow up of adverse events on study, including following up by phone, if required. Communicate relevant information to the physicians and medical staff in order to ensure the overall safety of subjects. Administer appropriate treatment as necessary. Maintain all me

#LI RB1 Qualifications #LI RB1

Provides application administration and technical support as the subject matter expert on all core business packages, including but not limited to Medidata, Rave, Oracle OC/RDC, Oracle Inform, SAS, and supplemental packages such as migration mentoring/review, reporting tools, custom functions, etc. Utilizes primary development tools and other supporting tools to design, w

#LI RB1 Qualifications #LI RB1

You're driven, resourceful, and above all else remarkably smart. This position serves as the day to day point of contact for multi project accounts (external and internal contact lead). The account executive oversees project and financial management functions for projects with limited management supervision, and assists manager with organic new business growth within exis

You are an expert facilitator you open doors, foster communication, and bridge the gap. In this role, you will be responsible for the management of defined accounts in a specified geographic region within the cardiac therapeutic area, specifically supporting our customers products. The FRS will execute the collaborative territory strategic plan through partnership with in

Performs other work related duties as assigned. Moderate travel may be required (up to 50%). Qualifications What we're looking for Bachelor's degree required; graduate degree preferred. Minimum of ten (10) years of experience in the healthcare industry in a sale, marketing, commercial operations and/or BD capacity. Experience in a selling capacity to pharmaceutical indust

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specifi

Oversees and ensures the completion of tasks required to support end users with the selection, onboarding, oversight and offboarding of Vendors/Vendor services used in support of clinical trial delivery Contributes details of Vendor capabilities and/or expertise in support of proposals and other Business Development initiatives. Supports customers with Vendor sourcing str

Maintains ownership of and manages contract process to ensure timely delivery and execution consistent with standard cycle times, including but not limited to, the coordination and finalization of the contractual instrument and budget to align with defined scope of work. Negotiates and prepares contracts, budgets and related documents for participation in complex clinical

Participates in regular reviews of assumptions and algorithms and identifies and implements required changes by collaborating with Proposals, Contracts, Change Orders, and Functional Group leaders. Collaborates with internal and external customers to understand their pricing related needs, and implements customized solutions. In the majority of cases, this involves workin

Act as central point of contact for all modules for end users for resolution of operational, process and advanced questions about system navigation and functionality (example data setup, site management, site monitoring, templates, filing, reporting, etc.). Provide business process and system expertise to support clinical project teams and functional teams regarding prope

Performs site qualification, site initiation, interim monitoring, site management and close out visits (performed on site or remotely) ensuring regulatory, ICH GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site specif

Development of protocols for clinical studies. Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Clinical Study Reports, Annual Reports and other Health Authority

Develop, validate and optimize bioanalytical methods by using analytical techniques. Process, analyze and interpret bioanalytical data. Responsible for finding solutions to problems related to the application of bioanalytical methods. Assist in improving laboratory activity processes (method development, validation and sample analysis). Write and review bioanalytical meth