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

Based at our Marlborough, MA site, as the Research Intern, you will serve as a critical contributor to a project focusing on the separation of subpopulations of nanoparticles using field flow fractionation technique. In this project, the candidate will perform fundamental studies on different nanoparticles, such as lipid nanoparticles, liposomes, extracellular vesicles, an

Based at our Marlborough, MA site, as the Research Intern, you will serve as a critical contributor to the development and integration of Sartorius' emerging technologies for characterization and purification of different types of nanoparticles such as extracellular vesicles and exosomes. These leading edge platforms will be utilized in basic research as well as the pharma

As the Research Intern, you will be expected to design and execute experiments systematically, analyze and report the results weekly. You willalso work closely with internal and external subject matter experts to identify and understand the nature of nascent technologies, including both characterization and purification systems. Based at our Marlborough, MA site, as the Re

1.Responsible for overall on site monitoring activities of assigned clinical sites. Includes but is not limited to a.Independently conduct all types of monitor visits, onsite qualifying site assessments, recruitment, initiation, for cause, interim and closeout, and/or remote visits as needed, in accordance with the Monitoring Plan. b.Perform source document verification/r

Reports to the Practice Manager and works under the direct super vision of the Physician(s), The Lead Clinical Office Coordinator assumes responsibility for a wide variety of administrative and supervisorial duties while supporting the Physician(s) clinical workflow and coordinating the administrative and clinical staff. Minimum Qualifications Education High School Diplom

Reports to the Practice Manager and works under the direct super vision of the Physician(s), The Lead Clinical Office Coordinator assumes responsibility for a wide variety of administrative and supervisorial duties while supporting the Physician(s) clinical workflow and coordinating the administrative and clinical staff. Minimum Qualifications Education High School Diplom

Basic Qualifications Bachelor's degree in Engineering, or a related Science, Engineering or Mathematics field, plus a minimum of 10 years of relevant experience; or Master's degree plus a minimum of 8 years of relevant experience. CLEARANCE REQUIREMENTS Department of Defense Secret security clearance is required at time of hire. Applicants selected will be subject to a U.

Coordinates the implementation, both internally and externally, of sponsored clinical research studies. Initiates and maintains recruitment contact with study participants. Responsible for screening applicants, ensuring they meet appropriate criteria, and makes independent judgement as to the suitability of their participation. May be required to perform clinical tests su

Spaulding Rehabilitation Hospital (SRH) is recruiting a Research Assistant to join the Cardiovascular Lab's Exercise for Persons with Disabilities (ExPD) Program. The ExPD Program is a one of a kind program that uses Functional Electrical Stimulation (FES) in conjunction with adaptive rowing ergometers to provide a unique opportunity for people with spinal cord injuries o

In order of importance, list essential 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. This section should be completed as a bulleted list and explain how the role is performed. Recruit, screen, schedule and conduct study vis

Completion of required personal certifications and renewals Training and overseeing new hires, including student externs, in informed consent procedures, structured interviews, and self report measures Community Relations Assist with preparation of newsletters Prepare recruitment materials Update lab website Participate in lab sponsored community events Scholarly activiti

The Clinical Research Coordinator (CRC) will perform research activities using approved techniques Procures, processes and ships research specimens and conducts patient recruitment, administers questionnaires, abstracts medical records, maintains patient databases, enters data into sponsor specific electronic data capture forms, performs administrative tasks, assists in g

of Role The Associate Director of Medical Affairs Field Excellence and Medical Operations is a key member of the Global Field Medical Affairs Team and will support the Senior Director of Medical Affairs Field Excellence and Medical Operations in the development, management, and execution of the Field Medical Affairs (FMA) operational plan and process improvement. The succe

In the Quality Control Lead role, you will assume responsibility for managing the QC activities that are pivotal in ensuring the quality and compliance of our new emerging therapy services. This includes the new GMP Phase 1 clinical production facility in Marlborough MA with the focus on novel modalities including allogenic stem cell, cell and gene therapy, extracellular v