- University of Pennsylvania (Philadelphia, PA)
- …wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist A Job Profile Title Clinical ... in the regulatory compliance and coordination of early phase clinical trials through the University of Pennsylvania Frontotemporal Degeneration Center.… more
- University of Pennsylvania (Philadelphia, PA)
- …of unit research, including but not limited to Phase I-IV clinical trials . The Regulatory Affairs Specialist C will, independently prepare and ... documentation/ Trial Master files (TMF) as required. The Regulatory Affairs Specialist C is expected to...but not limited to Phase I-IV clinical trials . The Regulatory Affairs Specialist … more
- University of Pennsylvania (Philadelphia, PA)
- …Posted Job Title Regulatory Affairs Specialist -CC Job Profile Title Clinical Research Regulatory Specialist B Job Description Summary The Abramson ... OCCR Regulatory Affairs Office seeks a full-time Regulatory Affairs Specialist -CC to participate in the...-CC to participate in the coordination of Phase I-V clinical trials . Reporting to the Regulatory… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Regulatory Affairs Start-Up Specialist Senior-CC Job Profile Title Clinical Research Regulatory Specialist C Job Description Summary The ... Regulatory Affairs Office seeks a full-time Senior Regulatory Affairs Start-Up Specialist to independently prepare...regulatory aspects of the initiation of Phase I-V clinical trials with a focus on required… more
- Johns Hopkins University (Baltimore, MD)
- …role responsible for study startup activities in interventional clinical trials . Classified Title: Regulatory Specialist II Role/Level/Range: ACRP/03/MB ... will serve as a central resource for faculty conducting clinical research. The Regulatory Specialist ...to facilitate study startup and maintenance of commercially sponsored clinical trials . Startup activities include coordination of… more
- Stanford University (Stanford, CA)
- …107768 The Blood & Marrow Transplantation and Cellular Therapy (BMT-CT) Divisionis seeking a Clinical Trials Regulatory Specialist II position to support ... Regulatory Specialist (Hybrid Opportunity) **School of...a very active clinical trials faculty. The position will anticipate and generate reports… more
- Houston Methodist (Houston, TX)
- …event reports, safety reports, and notifies IRB of study closures. + Maintains the required regulatory files for all clinical trials to ensure regulatory ... and study specific protocols/plans and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case… more
- J&J Family of Companies (Jacksonville, FL)
- …We are searching for the best talent to join our Vision team as a **Staff Clinical Trial Specialist ** located in **Jacksonville, FL** Fueled by innovation at ... to wellness. Learn more at https://www.jnj.com/medtech **Purpose:** The Staff Clinical Trials Specialist manages study...operating procedures and company policies are followed. The Staff Clinical Trial Specialist develops and… more
- Hackensack Meridian Health (Hackensack, NJ)
- …Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the field ... and overseeing clinical operations of all assigned clinical trials and participates in assessing, planning,...general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Education,… more
- Sumitomo Pharma (St. Paul, MN)
- …International Council for Harmonization E6(R2). + Fundamental knowledge of the conduct of clinical trials is preferred. + Strong focus on teamwork, attention to ... our website https://www.us.sumitomo-pharma.com or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be...ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure… more
- Houston Methodist (Houston, TX)
- …accurate data collection, documentation organization, and safety of study volunteers. Ensures accurate regulatory filing. + Assists Clinical Trial Manager in ... is responsible for supporting multiple projects under supervision of Clinical Trial Manager which may include ...from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research… more
- Tufts Medicine (Boston, MA)
- …explanation of facts, policies and practices. **Job Overview** This position supports clinical investigators, research administrators, clinical trials , and ... or related field. 2. Three (3) years' experience in clinical trials research or research administration **Preferred...with research personnel to identify and quantify information impacting clinical trial finances. 6. Serves as one… more
- J&J Family of Companies (Irvine, CA)
- … Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while encouraging strong, ... R&D Department to support execution of company sponsored clinical trials , ensuring compliance with timelines and...feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in… more
- University of Utah (Salt Lake City, UT)
- …Quality Oversight** + Conduct routine internal audits and targeted reviews of clinical trial documentation including regulatory binders, subject binders ... research study teams, and clinical teams, the QA Specialist ensures regulatory compliance, operational efficiency, and consistently high standards… more
- J&J Family of Companies (Irvine, CA)
- …and reporting to ensure trial validity. The Medical Affairs Clinical Specialist collaborates closely with cross-functional teams to support successful ... and Johnson Neurovascular is recruiting for a **Medical Affairs Clinical Specialist ** located in Irvine, California, USA....the clinical , medical and scientific lead for clinical trials in the J&J MedTech Neurovascular… more
- Edwards Lifesciences (Kansas City, KS)
- …clinical trial /study safety, in keeping with protocols, GCP (Good Clinical Practices) and regulatory requirements + Develop and deliver technical training ... make an impact:** + Field monitoring of studies and data collection for clinical trials , assess all data documentation, reports, records, transcripts, exam… more
- Stony Brook University (Stony Brook, NY)
- Research Nurse - Cancer Clinical Trials **Position Summary** The **Research Nurse** for the Cancer Center Clinical Trials Department is responsible for ... AE logs, con meds, etc.) in source material, and enter necessary information into Clinical Trial Management System (CTMS). + Assist with organizing, and attend… more
- Insight Global (Irvine, CA)
- …timelines. Collaborate with cross-functional teams ( Regulatory , Data Management, Clinical Operations) to ensure smooth trial execution. Maintain accurate ... role is critical in ensuring high-quality site management and operational excellence across clinical trials . Key responsibilities include but are not limited to:… more
- University of Washington (Seattle, WA)
- …in compliance with evolving regulatory requirements. **Position Purpose** **:** Clinical Research Billing Specialist position will enable the Clinical ... and ranking among the top research universities internationally. The Clinical Trials Office (CTO) supports the ...global biotech and biopharma sponsors, the availability of funded clinical trial opportunities in UW pipeline, and… more
- AbbVie (North Chicago, IL)
- …the ACPRU clinical trial subject recruitment system in support of clinical trials conducted at the ACPRU. Ensure compliance with all applicable policies, ... trial timelines and organizational objectives. Responsibilities + Manages and optimizes clinical trial subject recruitment systems. + Drive initiatives to… more