- Merck & Co. (Rahway, NJ)
- … Manager on study deliverables.Participates in the set up and design during study start up (eg, database set up)Lead medical monitoring team in review and ... Job DescriptionPosition Description: Associate Director, Clinical Scientist This position drives scientific...scientific planning, strategy and execution of Phase 1-4 clinical studies . Under the direction of the Program Lead, you… more
- Edward Jones (Kalaheo, HI)
- …streamlined client experience consistent with firm policies and procedures, regulatory requirements, and ethical guidelines.Engage the branch team to create, ... registrations may be obtained at Edward Jones during the assigned paid study period.FINRA registrations required within three months. State insurance licenses will… more
- ICON Clinical Research (Brentwood, TN)
- …to the Central CDP Review Team (CDPRT) and Sponsor. **What you need for Study Start Up Associate I - Regulatory Submissions** * A high school diploma or ... Study Start Up Associate ... Study Start Up Associate II - US,...regulatory and site level critical documents required for study site activation in accordance with ICON SOPs/WPs, Sponsor… more
- Dana-Farber Cancer Institute (Boston, MA)
- …reporting for the DFCI. The CRM will be supervised and supported by the Associate Director of Cohort Studies to develop and implement strategies that will ... Studies program. + Initiates, plans, facilitates and oversees the research project start -up, active and close out phases; for studies and activities within… more
- Colorado State University (Fort Collins, CO)
- … studies are conducted according to protocol and meet regulatory requirements. Percentage Of Time20 Job Duty CategoryStudy Conduct Procedures Duty/Responsibility ... Posting Detail Information Working TitleRA II - Study Lead, ARPA H Position LocationFort Collins, CO...studies are conducted according to protocol and meet regulatory requirements Percentage Of Time10 Application Details Special Instructions… more
- Actalent (Basking Ridge, NJ)
- …for Operational Study Strategy. Responsibilities + Develop project cross-functional, integrated study plans to study start -up (in-house) and validate and ... Study team. This role is primarily a tactical study delivery role, reporting into an Associate ...documents are created in a timely manner ahead of study start . + Coordinate with the CRO… more
- Battelle Memorial Institute (Columbus, OH)
- …quality control (QC) in electronic data acquisition systems + Assist with study start preparation activities including requests for equipment, ordering ... critical services for our clients-whether they are a multi-national corporation, a small start -up or a government agency. We recognize and appreciate the value and… more
- Cargill (Wichita, KS)
- …around the world and connect with something greater. **Food Safety, Quality, and Regulatory Associate Position:** The purpose of this position is to develop ... if your ideas could nourish the world? As an associate , we transfer your knowledge and skills into profound...of increased complexity across the Food Safety, Quality, and Regulatory (FSQR) job family at various locations across Cargill.… more
- Penn Medicine (Plainsboro, NJ)
- …regarding process. Ensure process moves steadily to completion, clear roadblocks to study start up.COMPLIANCE: Perform group-specific regulatory activities, ... research portfolio. This employee will oversee the processes for study start -up and on-going study ...start to finish working closely with the CRU Regulatory coordinators to manage, review, and initiate trials to… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …Gilead's products. You will support other Clinical Operations team members in the start -up, maintenance and close-out of clinical studies . You may manage certain ... studies and act as a member of the study team. You may also lead clinical studies...optimize project efficiencies and effectiveness. + Provides oversight of study sites and reviews routine regulatory documents… more
- Abbott (Alameda, CA)
- …generating monitoring trip reports, and track resolution of action items. + Participate in study start up activities. + Responsible for ensuring shipment of ... but not limited to planning and implementation of clinical studies from concept to clinical study report...+ Participate in the interim and final reviews of study data in preparation of regulatory submissions.… more
- University of Michigan (Ann Arbor, MI)
- …space in person + Design work flow and develop quality assurance processes for study start up, execution and conduct. Maintain accurate research records and ... Now **Job Summary** This clinical research coordinator (CRC) position may provide study coordination for multiple clinical research studies depending on… more
- BeiGene (San Mateo, CA)
- …, Global Study Management Associate , Clinical Research Associates and Study Start -up Specialists). + As required, supports CRAs with various activities ... and budget. + Supports the Clinical Research Associates and/or Study Start -up Specialists in country study...Regional Clinical Study Manager and the Global Study Management Associate . + Supports the TMF… more
- Hartford HealthCare (Bridgeport, CT)
- …efforts to initiate new studies , attending IRB meetings to expedite the start -up process. The SrCRA supervises all study activity and may delegate ... analysis and development of protocols. * Enrolls patients in studies by screening for eligibility criteria, consulting with physicians...study activity as required of a Clinical Research Associate This is an onsite position** * Bachelor degree… more
- Amgen (Thousand Oaks, CA)
- …and Supply Planning processes. The GSP Ensures Finished Drug Product supplies from study start throughout last patient dosed and is involved throughout the ... the lives of patients while transforming your career. **Senior Associate Supply Chain** **What you will do** Let's do...durations of the clinical studies and programs until … more
- Stanford University (Stanford, CA)
- …include*: + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Cancer Clinical Research Coordinator Associate - Sarcoma (Hybrid) **School of Medicine, Stanford,...enroll and follow patients on trial and assist with regulatory and financial requirements of the trials. We are… more
- Abbott (Philadelphia, PA)
- … study team, Site Contracts Associate ), as needed. **Manage all aspects of study lifecycle to include site regulatory and quality:** + ** Start Up** + ... all aspects of the start -up process and site initiation visits + Understand regulatory and legal requirements for study participation at a level that allows… more
- Stanford University (Stanford, CA)
- …contact with research participants, sponsors, and regulatory agencies. + Coordinate studies from start -up through close-out. + Determine eligibility of and ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...gather consent from study participants according to protocol. Assist in developing recruitment… more
- Stanford University (Stanford, CA)
- …include:** + Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start -up through close-out. ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States**...+ Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment… more
- IQVIA (Durham, NC)
- …Escalate quality issues as appropriate. + Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, ... IQVIA MedTech is seeking a Clinical Research Associate II with Medical Device monitoring experience! Central...management work to ensure that sites are conducting the study (ies) and reporting study data as required… more
