- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO ... data collection and entry into paper and electronic databases, maintenance of clinical research supply inventory, processing clinical trial billing… more
- IQVIA (Overland Park, KS)
- …customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.You should have: + A Bachelor's degree in ... As you develop your career as a CRA , this role offers you the opportunity to...\#C1920 \#CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- Touro University (Hawthorne, NY)
- …adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Responsibilities ... with clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research . + Monitor study patients for adverse events in… more
- Abbott (Alameda, CA)
- …in life sciences preferred or equivalent with minimum one (1) year of clinical research experience, or combination of appropriate education and experience. + ... working mothers, female executives, and scientists. **The Opportunity** The CRA will ensure quality, accuracy, and integrity of ...CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple… more
- IQVIA (Carlsbad, CA)
- IQVIA is seeking Study Start-Up Clinical Research Associates to join our Sponsor Dedicated teams. Ideal candidates will have experience in Study Start-Up and at ... travel up to 70-80%. Job Overview The Study Start-Up CRA is accountable for site selections as well as...sponsor strategy IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
- BeOne Medicines (Emeryville, CA)
- …follow-through with audit/inspection findings to resolution as it related to involved CRA staff. * Assist with other assigned clinical responsibilities within ... site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with… more
- SUNY Upstate Medical University (Syracuse, NY)
- …of education and experience. SoCRA certified or ACRP certified Experience with clinical research protocols, knowledge of medical terminology, computer skills, ... Job Summary: Position is Project Manager for a large multi-site clinical trial. Train and oversee CRA 's on the project. Clinical Site is also Coordination… more
- SUNY Upstate Medical University (Syracuse, NY)
- …experience or equivalent combination of education and experience, experience with clinical research protocols, knowledge of medical terminology, computer skills, ... written/oral communication and organizational skills required. Preferred Qualifications: Previous clinical research experience with cardiology patients and SOCRA… more
- SUNY Upstate Medical University (Syracuse, NY)
- …Institutional Review Board and regulatory agencies. Enroll, register and screen patients for clinical research trials; collect and submit clinical trial ... proper collection and shipment of lab samples; billing support; maintenance of clinical research study supplies and drug accountability. Minimum Qualifications:… more
- Queen's Health System (Honolulu, HI)
- RESPONSIBILITIES I. JOB SUMMARY/RESPONSIBILITIES: * Conducts clinical research studies under the immediate direction of assigned Principal Investigator. * ... Assists researchers, clinical and administrative personnel in performing a variety of...personnel in performing a variety of duties on a research project. II. TYPICAL PHYSICAL DEMANDS: * Essential: standing,… more