In this role, you will serve as an individual contributor within a team; upon the direction and guidance of leadership, you will be responsible for supporting the goal of meeting scope, schedule and delivery requirements. Primary expectations of a Researcher I include Responsible for outreach, recruiting, screening, scheduling, and tracking of research participants Plans

You are as unique as your background, experience and point of view. Here, you'll be encouraged, empowered and challenged to be your best self. You'll work with dynamic colleagues experts in their fields who are eager to share their knowledge with you. Your leaders will inspire and help you reach your potential and soar to new heights. Every day, you'll have new and exciti

Direct report (project manager) expected within 1 2 years PATIENT CONTACT None Qualifications Master's degree in cancer, genetics, genomics, or research required. Previous experience in the conduct of clinical trials and research operations required. 10 years of increasing expertise and responsibility in regulatory and specimen based research required. Experience in proje

Utilize MS Access, Excel and REDCap to assist in data collection efforts, database development, and descriptive data analysis. (In house REDCap and MS Access training is available.) Assist with preparation of Institutional Review Board(IRB) documentation and forms for study protocol approvals and amendments. Schedule conference calls; prepare agendas and pre meeting mater

Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation. 1. Coordinates the implementation, both internally and externally, of sponsored clinical research studies. 2. Initiates and maintains contact with study participant

Indicate key areas of responsibility, major job duties, special projects and key objectives for this position. These items should be evaluated throughout the year and included in the written annual evaluation. 1. Provides assistance on clinical research studies as per study guidelines and protocols. 2. Recruits and evaluates potential study patients. Per protocol instruct

The Clinical Research Specialist coordinates and oversees the implementation of recruitment and other operations activities for multiple, concurrent clinical research studies/trials, with responsibilities including Program Communication Strategize with staff when problems arise and offer potential solutions. Ensure uniform application of regulatory requirements across all

Identifying and recruiting patients to participate in research Attending patient appointments and procedures to collect research samples and data Processing, storage, and management of biospecimens from study participants Maintenance of regulatory documentation for all study participants Medical chart review and data abstraction Study and protocol coordination, revision,

Perform administrative support duties to assist the investigative team Attend individual and team meetings Conduct literature review and library searches Assist with developing and managing IRB protocols for the study Assist with recruiting patients for clinical trials Verify subject inclusion/exclusion criteria Provide basic explanation of study and obtains informed cons

At Boston Children's Hospital, the quality of our care and our inclusive hospital working environment lies in the diversity of our people. With patients from local communities and 160 countries around the world, we're committed to reflecting the spectrum of their cultures, while opening doors of opportunity for our team. Here, different talents pursue common goals. Voices

Mechanical Engineer Location US NJ Parsippany | US MA Boston | US NY Albany Job ID 6549 # Positions 1 Category Energy Management WHY CHA? Finding a better way. At CHA, we believe in the power of clean water, resilient energy, safer roads, and structures that harmoniously blend with their surroundings. We create solutions. We help People. We improve our world. At CHA, we e

Summary Under general supervision coordinates and/or initiates the identification recruitment and follow up of patients participating in one or more clinical research studies. Collaborates with physicians/investigators and other members of healthcare team to promote explain and assist in implementation of clinical investigation studies. Collects data and monitors patient

Summary Under supervision and following established policies and procedures conducts experiments using in vivo/or in vitro techniques. Performs minor surgery on animals. Operates monitoring equipment; collects and analyzes data using statistical methodology. Reviews literature in the field for informational purposes or to gather data. Responsibilities Calibrates and sets

Analytics Engineer 2 Job Location US MN Center City | Other Remote Office ID 2024 11230 Status Full Time Shift Day Schedule Mon Fri Hours of Work 8 00 4 00 Responsibilities The Analytics Engineer will ensure data is ingested, transformed, scheduled, and enabled to meet the analytics needs of the organization. They are responsible for designing, implementing, and maintaini

Parexel is seeking a Clinical Trial Oversight lead in the Mid West US! Position Purpose The Clinical Trial Oversight Lead (CTOL) is responsible for the following Oversight of outsourced monitoring activities to ensure adherence to the protocol, Good Clinical Practice (GCP), evolving regulatory requirements and assess monitoring effectiveness. The CTOL will ensure that the