- Trinity Health (Fort Lauderdale, FL)
- …**Description:** Summary This person will be responsible for the conduct of multiple clinical research activities. Ideal candidate will have industry sponsored ... Person is able to work with minimal supervision and within the scope of clinical research protocols, participates in research activities which may include:… more
- Abbott (Alameda, CA)
- …+ BS degree in life sciences or equivalent with minimum 5 years of clinical research experience + Must have 2+ years of relevant experience in ... and to be flexible when priorities change. + Working knowledge of GCP, Clinical and Regulatory Affairs. + Proficient with Microsoft Suite. **Travel… more
- AbbVie (Dayton, OH)
- …Description The CRA II advances AbbVie's pipeline by striving for excellence in clinical research , turning science into medicine for our patients and leveraging ... trials. Lastly, the CRA II focuses on site clinical research that ensures appropriate conduct of...all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site… 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 ... pre- clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment,...clinical team. + Ensure compliance with the Good Clinical Practice guidelines in clinical research… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I (CRA I) will join a team of experienced associates and manage various research trials, including first in ... all managed studies. The CRA I will interact daily with clinicians, sponsors, IRB, regulatory agencies and other research professionals. This is a subject /… more
- IQVIA (Parsippany, NJ)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have: + A Bachelor's ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- ICON Clinical Research (NC)
- As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... work in United States without visa sponsorship + A clinical research professional with 2+ years of...Lung Cancer) and Hematology + Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS… more
- ManpowerGroup (Lake Forest, IL)
- **Title:** Clinical Research Associate (CRA) **Location:** Lake forest, IL **Duration:** 12 Months **Remote role (occasional travel)** **Pay Range :** $25/hr ... $29/hr (On W2) We are looking for a " ** Clinical Research Associate (CRA)"** to...close-out visits + Ensure compliance with protocols, GCP, and regulatory requirements + Perform source document verification and data… more
- IQVIA (Overland Park, KS)
- …and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.You should have: + A Bachelor's ... our team** . \#C1920 \#CRAFSAJD IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… 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
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