Coordinates the implementation, both internally and externally, of sponsored clinical research studies. Initiates and maintains contact with study participants. Help screen applicants, ensuring they meet appropriate criteria, and makes independent judgment as to the suitability of their participation. May be required to perform clinical tests such as phlebotomy, EKGs, etc

Provides assistance on clinical research studies as per study guidelines and protocols. Recruits and evaluates potential study patients. Per protocol instruction, conducts telephone interviews or schedules patient for study visit and screening. May be required to perform clinical tests such as questionnaires, phlebotomy, EKGs, etc. if certified and as needed. Will work in

Please note, the functions below are representative of major duties that are typically associated with these positions. Specific responsibilities may vary based upon departmental needs. Similarly, not all duties that have been outlined will be assigned to each position. Assists with screening across multiple ICUs and procedural/operating room areas, maintaining a screenin

The following job duties will be performed under general supervision by the Clinical Research Manager Assist clinical team in screening potential patients for study participation Schedule all protocol required tests and procedures Coordinate patient appointments with physicians, nurses, and all test areas Coordinate and schedule clinical safety laboratory specimen draws a

Site Name USA Pennsylvania Upper Providence, Durham Blackwell Street, UK Hertfordshire Stevenage, Waltham Posted Date May 3 2024 The Strategic External Development (SED) team is an empowered, innovative, and agile CMC development organization within MDS that will unlock the potential to rapidly deliver an increased number of transformative medicines to patients through ex

ImmunityBio, Inc. is a late stage immunotherapy company developing a broad pipeline of next generation therapies that drive immunogenic mechanisms for defeating cancer and infectious disease. The company's immunotherapy platform is designed to activate both the innate (natural killer cell and macrophage) and adaptive (T cell) immune systems to create long term "immunologi

Conduct high quality research in kinesiology or related fields. Seek and secure external funding for research activities. Publish research findings in peer reviewed journals and present at national and international conferences. In instances where research findings are deemed proprietary by study sponsors, generate appropriate reports Collaborate with other faculty member

Under the supervision of the Principal Investigator (PI), the candidate will perform activities on multiple research projects. The candidate will be expected to work with a high level of independence, prioritize all aspects of research activities with minimal supervision, and self initiate suggestions and approaches to research efforts. Research populations will include t

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator I is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary

Principal duties may vary over time with grant funding and project demands, and with skill level of other staff assigned to projects. Evaluates and recruits potential study participants. Interacts with potential study participants, educating them about the studies including the possible risks/benefits, procedural details, and significance of the studies. Obtains informed

1. Oversee three to four active clinical studies; tasks include the planning, development, and implementation of clinical protocols. 2. Manage recruitment, screening, enrollment, consenting and conducting study visits of clinical research subjects. 3. Collect and enter data and manage study databases. 4. Preparation and submission of research protocol to the IRB. 5. Ensur

None EEO Statement BWH is an Affirmative Action Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other s

Use bioinformatics platforms to support clinical research in virology Perform statistical analysis and interpretation of the data. Contributes to scientific literature, reports, journals and presentations. Qualifications QUALIFICATIONS MS degree or equivalent education in scientific field of research required. M.D. preferred Five to seven years of direct research experien

The CRC will work on a variety of projects to support the CVE. The CRC reports jointly to the SCRPM and the Director of the CVE. Subject Screening / Enrollment Develops and implements recruitment strategies Assists with screening, informed consent, and enrollment of patients Verifies subject inclusion/exclusion criteria Obtains informed consent from subjects Conducts subj

Convene and provide overall direction to project teams, which may consist of data staff, research associates, research coordinators and faculty, for the development of project statements, work plans, study designs, grant applications, literature reviews, analysis plans, and project deliverables. Identify necessary resources to perform project work, monitor work progress i