- Actalent (Bronx, NY)
- …grading scales. + Complete Serious/Unexpected Adverse Event forms as required by study sponsors, federal requirements, and institutional guidelines. + Provide ... Job Title: Sr. Clinical Research Coordinator Job Description We are seeking... trial protocols. This role involves developing and preparing study tools, collaborating with research professionals, and ensuring compliance… more
- University of Colorado (Aurora, CO)
- …management systems)._ **_Knowledge, Skills, and Abilities:_** + _Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)._ + _Ability ... ** Clinical Research Professional** **Description** **University of Colorado Anschutz...Responsibilities: + Act as a Primary Coordinator on multiple trials/ studies , managing the day-to-day operations. + Develop protocol-specific source… more
- Terumo Neuro (Aliso Viejo, CA)
- …direction to clinical study teams and cross-functional partners; ensuring clinical studies are conducted to the highest ethical and safety standards. Job ... and/or standards governing the conduct of clinical studies (eg, 21 Code of Federal Regulations...development, execution, and closure. 10. Ability to concisely interpret clinical study results, safety reporting, data integrity,… more
- Baystate Health (Springfield, MA)
- …visits. 15) Adheres to protocol, IRB, HIPAA, and regulatory requirements. **Required Work Experience:** **1)** 2 years of clinical research experience or ... **Summary:** **Job Responsibilities:** **1)** Assists with moderately complex study tasks in accordance with protocol guidelines. **2)**...HS/AD with 1+ years of clinical research experience **Preferred Work Experience:** **1)**… more
- Cedars-Sinai (Beverly Hills, CA)
- …per week. If hired you must reside in the commutable area.** The Clinical Research Coordinator II works independently providing study coordination including ... **Job Description** **This role follows a hybrid work schedule; however, we can only consider applicants...sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data,… more
- Merck (Upper Gwynedd, PA)
- …Director may: Supervise the activities of Clinical Scientists in the execution of clinical studies . Work closely with a cross-functional group of experts ... Director may be responsible for: Analyzing and summarizing the clinical findings from studies to support decisions...safety and efficacy as well as new drug applications, clinical study reports, or publication; and participating… more
- Arkansas Children's (Little Rock, AR)
- …The Clinical Research Professional I coordinates selected specific aspects of clinical research studies . This role serves as a resource for research ... the clinical research team regarding specified aspects of the study . **Additional Information:** **Required Education:** High school diploma or GED or equivalent… more
- Fresenius Medical Center (Mishawaka, IN)
- …profit and loss, subject enrollment strategy, and staffing, potentially at multiple clinical research site locations. Ensures research studies are conducted ... and procedures as well as all applicable State and Federal regulations under supervision of the Principal Investigator (PI)...date for all staff-research or facility support-as required per study protocols. * Assists with ensuring clinical … more
- University of Southern California (San Diego, CA)
- …to: + Oversees Clinical Monitors for sponsor and investigator initiated clinical research + Responsible for managing study site assignments, daily ... for clinical monitoring procedures + Serves as primary communications liaison for clinical monitoring and study teams + Develops and administers ongoing … more
- University of Michigan (Ann Arbor, MI)
- …2. Ethical Participant Safety Considerations 3. Investigational Products Development and Regulation 4. Clinical Study Operations (GCP's) 5. Study and Site ... We are looking for a personable, self-motivated, and organized Clinical Research Assistant to help with study ...+ At least six months of previous research experience, clinical /hospital work or volunteer experience, and/or knowledge… more