- IQVIA (Durham, NC)
- …prior monitoring experience. * Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements (ie, Good Clinical Practice ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… 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 degree ... or at least three months of on-site monitoring experience. 2 years of clinical research coordinator experience strongly preferred. + Alternatively, you should… more
- IQVIA (Philadelphia, PA)
- …and owning local trial activites at the regional level._** **Additional Information** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an ... - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws,… more
- Parexel (Austin, TX)
- **Job Purpose:** The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned ... study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The...Data Scientist) + May act as a Mentor for Clinical Research Associates **Skills:** + Monitoring Experience:… more
- Cedars-Sinai (Los Angeles, CA)
- …successful implementation of ASPIRE's goals through culturally responsive outreach and collaboration. The Clinical Research Associate I works directly with a ... assist in designing data collection/abstraction tools. Enters and processes clinical research data into sponsor -provided...experience preferred. **Req ID** : 13883 **Working Title** : Clinical Research Associate I (Hybrid,… more
- Hartford HealthCare (Hartford, CT)
- …turn to us. *Job Summary:* As a specialized research professional the Clinical Research Associate (CRA) collaborates with the Principal Investigator (PI) ... these duties, the CRA works with the PI, department, sponsor , IRB and institution to support and provide guidance...all aspects of study activity as required of a Clinical Research Associate * *… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 12/01/2025 **Requisition Number** PRN43704B **Job Title** Clinical Research Management **Working Title** Associate Director, ... contracts to align with department and institutional goals and sponsor expectations. + Represent the department and research...hire employee at one of the following job levels:** ** Associate Director, Clinical Research :** Requires… more
- Cedars-Sinai (Los Angeles, CA)
- …pulses through Cedars-Sinai. **We invite you to consider this phenomenal opportunity!** As a Clinical Research Associate I, you will work under the direction ... external sponsors for select trials. + May respond to sponsor inquiries and attend meetings regarding study activity under...the most. **Req ID** : 13223 **Working Title** : Clinical Research Associate I -… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** **Come join our team!** The Clinical Research Associate II works independently but in close collaboration with a Clinical Research ... contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities. +...the most. **Req ID** : 13839 **Working Title** : Clinical Research Associate II -… more
- Cedars-Sinai (Los Angeles, CA)
- …| Cedars-Sinai **Are you ready to be a part of breakthrough research ?** The Clinical Research Associate I will work directly with a Clinical ... trials. + Assists with preparing manuscripts, letters, and other research documents as needed. + Responds to sponsor...the most. **Req ID** : 12957 **Working Title** : Clinical Research Associate I -… more
- Parexel (Boston, MA)
- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... local country regulations + Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) +… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: The Clinical Research Associate I will be responsible for the coordination of clinical research studies within the Department of ... data collection and entry into paper and electronic databases. Maintenance of clinical research supply inventory, processing clinical trial billing… more
- Vitalief (Phoenix, AZ)
- …achieve sustainable growth. THE ROLE We are seeking a highly skilled and motivated Clinical Research Associate (CRA) to support our pharmaceutical client, ... costs, and accelerate breakthroughs that improve patient care. We bring deep clinical research expertise together with practical, results-driven consulting to… more
- Kelly Services (Jacksonville, FL)
- **In-House Clinical Research Associate I** Hybrid: Onsite Monday - Wednesday **Top Required Skills:** + Medical Device experience or Ophthalmology + 1-3 ... demonstrate professional conduct when interacting with investigational site personnel and sponsor representatives. + Monitor Clinical Research Organizations… more
- Parexel (Baltimore, MD)
- **Job Title:** Entry level Research Associate (per diem) ** Clinical /Data Entry** **Work Location:** onsite in Baltimore, MD (some of the data entry work can ... is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of… more
- Ochsner Health (Covington, LA)
- …bachelor's degree. Preferred - 2 years of experience in area of assigned clinical specialty, managing clinical research and patient databases. ... all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, research ...Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Ability… more
- Actalent (Gaithersburg, MD)
- Job Title: In-House Clinical Research Associate Job Description We are seeking a skilled Clinical Research Associate to join our dynamic ... by the supervisor. Essential Skills + Experience in vendor management and clinical research . + Proven monitoring oversight experience, including co-monitoring or… more
- Ochsner Health (New Orleans, LA)
- …status. **Knowledge Skills and Abilities (KSAs)** + Knowledge of medical and clinical research terminology and processes. + Familiarity with ICH guidelines ... High school diploma or equivalent. **Work Experience** Required - 1 year of relevant research or clinical experience, OR Bachelor's degree in life science or… more
- Parexel (Richmond, VA)
- …Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility for the delivery ... associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). + Ensures timely collection/uploading of… more
- IQVIA (Overland Park, KS)
- Job Overview: Join our dynamic team as a Clinical Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ... ensure compliance with study protocols, regulations, and sponsor requirements. Be at the forefront of groundbreaking...from you! IQVIA is a leading global provider of clinical research services, commercial insights and healthcare… more
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