- University of Pennsylvania (Philadelphia, PA)
- …oversee all aspects of the clinical research portfolio. He/she will oversee the start -to-end processes for study start -up and ongoing study ... programs and resources, and much more. Posted Job Title Clinical Research Program Manager B (Abramson Cancer...transporting specimens, data entry, query resolution and working with study monitors). The Program Manager will work… more
- University of Pennsylvania (Philadelphia, PA)
- … will independently manage a portfolio of Phase I Penn-Sponsored clinical research studies . The Sr. Clinical Project Manager is responsible for the ... execution and management of their assigned projects, from initial study start -up to study close/database... clinical trial processes, and the conduct of clinical studies . Reference Information: The salary range… more
- University of Pennsylvania (Philadelphia, PA)
- …with all regulatory organizations. S/he will play a key role in study start -up, intake & feasibility for many studies . The Project Manager will ... in the study protocols. The Project Manager will manage/supervise the study teams assuring that each clinical trial meets expectations and that they are… more
- University of Pennsylvania (Philadelphia, PA)
- …in order to ensure execution of clinical research and oversee clinical studies from concept to final close, including study start -up activities, ... and resources, and much more. Posted Job Title Senior Clinical Trial Project Manager (Center for Cellular... clinical trial processes, and the conduct of clinical studies . Salary: The job pay range… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Operations Manager , Abramson Cancer Center Clinical Research ... Unit Job Profile Title Clinical Research Program Manager C Job Description Summary The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world… more
- University of Pennsylvania (Philadelphia, PA)
- …approved protocols, according to Good Clinical Practice. Obtain detailed knowledge start -up activities and of all components of study protocols by review ... Responsibilities + Assist in the initiation and conduct of clinical research studies performed by physicians using...of study protocol, related literature prior to study start date. Assure accurate and timely… more
- University of Pennsylvania (Philadelphia, PA)
- …B (CRC-B): Duties include, but are not limited to: + Assisting with study start -up activities: drafting initial IRB protocol(s), SOPs, recruitment fliers, case ... IND, and GCP guidelines by all personnel involved in clinical studies . + Assist in the preparation...relevant bodies, and may supervise other lab members in clinical study -related activities. Effective problem-solving abilities; effective… more
- Terumo Medical Corporation (Somerset, NJ)
- Sr. Manager , Clinical Advisors Date: Aug 27,...reports. Clinical operational activities: + Support trial study start -up phases (support in writing ... wherever we go next!** **_Advancing healthcare with heart_** **Job Summary** Senior Manager , Clinical Advisor is responsible for developing and implementing the… more
- University of Pennsylvania (Philadelphia, PA)
- …study protocols by review of study protocol, related literature prior to study start date. Schedule and conduct follow-up visits with patients and ensure ... manner. Monitor adherence to protocol throughout patient enrollment in study . Notify PI, project manager of any...changes in consent. + Assist in the conduct of clinical research studies performed by physicians using… more
- University of Pennsylvania (Philadelphia, PA)
- …compliance with standard processes, policies and procedures. + Play a key role in study start -up, intake and feasibility. + Facilitate and support audits and ... resources, and much more. Posted Job Title Expanded Grants Manager , Center for Clinical and Translational Research...compliance with other sponsor guidelines + Provide support to study team, present financial and compliance status with team… more
- University of Pennsylvania (Philadelphia, PA)
- …packages + Corresponding with sponsor & regulatory review boards + Assisting with study start up activities + Screening, recruiting, and consenting patients ... enrollment, study visits and regulatory compliance in one or more studies . POSITION CONTINGENT UPON FUNDING Job Description Clinical Research Coordinator B… more
- University of Pennsylvania (Philadelphia, PA)
- …Planning and implementation of study protocols. Manage regulatory aspects of clinical research studies (eg IRB submissions, CTSRMC submissions, study ... Summary This position will support the management of 8-10 clinical research studies (all phases) that involve...and communicating frequently with sponsors, CROs, and coordinating site study teams. He/she will oversee all start -up… more
- University of Pennsylvania (Philadelphia, PA)
- …with all regulatory organizations. S/he will play a key role in study start -up, intake & feasibility for many studies . The Project Manager will ... protocols. The Project Manager will manage/supervise the study teams assuring that each clinical trial...compliance checks and helping teams prepare for audits. Lead study intake and drive study start… more
- University of Pennsylvania (Philadelphia, PA)
- …and submission of regulatory documents to the Institutional Review Boards and will support the study team in new study start up activities. Qualifications + ... research studies . Coordinating duties will include screening and enrolling study participants, completing the informed consent process, administering study … more
- Bristol Myers Squibb (Princeton, NJ)
- …Internal: Global Trial Manager (GTM), Clinical Trial Managers (CTMs) Clinical Trial Monitors (CTMos), Study Start -up Specialists, Site Contract ... key internal matrix relationships and key external stakeholders/clients + External: Clinical Study Sites, Institutional Review Boards/Ethics Committees, Vendors,… more
- University of Pennsylvania (Philadelphia, PA)
- … study binders, regulatory binders (hard and electronic version), enrollment log for study start -up + Ensure preparation of all required study related ... patients, subject enrollment, collection and storage of biological samples and related study documents, and collection of clinical data. Assist with… more
- University of Pennsylvania (Philadelphia, PA)
- …and supplies, monitor project timelines and reporting. + Manage single and multi-site clinical trials (including study start -up, daily operations, and ... partners to effectively operationalize research studies and clinical trials. Job Description The LCNS lab manager...will ensure harmonization of study activities across studies . The lab manager will also serve… more
- University of Pennsylvania (Philadelphia, PA)
- …phases. The Research Manager will help develop, coordinate, and execute clinical studies aimed at improving screening for underdiagnosed diseases and ... Manager will help design, organize, and execute several clinical research studies aimed at improving screening...research, including ongoing investigator-initiated studies and new studies that are in development or start -up… more
- University of Pennsylvania (Philadelphia, PA)
- …is contingent upon favorable funding. Job Responsibilities + Manage single and multi-site clinical trials (including study start up, regulatory submissions, ... for day-to-day management of complex projects conducted by the study team. The Research Project Manager will...will ensure harmonization of study activities between studies . The Research Project Manager will be… more
- Merck (Trenton, NJ)
- …to IRB/ERC and Health Authorities. The role will collaborate at local level closely with Clinical Operation Manager COM , Clinical Research Manager CRM ... (eg Safety Reports) + Ensure collation and distribution of study tools and documents + Update clinical ...start -up and submissions + Obtain, track and update study insurance certificates + Support preparation of submission package… more