- Olympus Corporation of the Americas (Center Valley, PA)
- …database amendment implementation. + Study level coordination and hands-on CDM tasks, including clinical data review and reconciliation. + Authors data ... key data management deliverables used to collect, review , monitor, and ensure integrity of clinical data , oversees application of industry standards, … more
- Pfizer (Groton, CT)
- … study results Support execution for all FIH programs through proof-of concept Set the clinical data review strategy, ensure quality data and conduct ... review of emerging clinical data and trends; review and query data ; present and discusse relevant data to appropriate teams, governance bodies,… more
- Arvinas (New Haven, CT)
- … Review and Analysis** + Lead development of Medical Monitor Plans + Perform ongoing clinical data review and critical analysis of study data ... a substantial role in the development of the clinical documents, the review of scientific and clinical data and the communication of data to the… more
- GRAIL (Menlo Park, CA)
- …consistent, and accurate. + Perform study startup activities such as study protocol review , Clinical Data Management Plan (CDMP) development, and Electronic ... For more information, please visit grail.com . The Senior Clinical Data Manager (CDM) will lead ...Manage study conduct activities including facilitation of study team data review , documentation of data … 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 ... be done remotely after training) **Parexel Early Phase Clinical Unit** supports the development of innovative new medicines...and set documentation standards for staff to follow. + Review , monitor and address quality of data … more
- NORC (Chicago, IL)
- …prescribing practice requirements, and interpretations of comparative effectiveness of outcomes based on clinical trial data + Utilize data and literature to ... to pharmaceutical drug prescribing practices + Develop protocols for and conduct clinical trial literature reviews and data extraction. + Conduct systematic… more
- CEDARS-SINAI (Los Angeles, CA)
- …protocol and research objectives. Responsible for completing case report forms, entering clinical research data , and assist with regulatory submissions to the ... Administrator or Research Nurse to coordinate/implement study. Evaluates and abstracts clinical research data from source documents. Ensures compliance with… more
- Christus Health (Wake Village, TX)
- …per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data , conducts monitors and ... overseeing the preparation and dispensing of medications. Performs duties in the clinical areas assigned such as but not limited to: anticoagulation clinics,… more
- Christus Health (New Chapel Hill, TX)
- …per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data , conducts monitors and ... overseeing the preparation and dispensing of medications. Performs duties in the clinical areas assigned such as but not limited to anticoagulation clinics,… more
- Christus Health (Converse, TX)
- …per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data , conducts monitors and ... overseeing the preparation and dispensing of medications. Performs duties in the clinical areas assigned such as but not limited to: anticoagulation clinics,… more
- Canfield Scientific, Inc (Parsippany, NJ)
- … clinical , commercial or regulatory activities Prepare, write, and review study documentation, including protocols, qualitative study reports, and study-related ... services for the pharmaceutical, biotechnology and cosmetics industries supporting global clinical trials providing primary endpoint data and supporting… more
- CEDARS-SINAI (Los Angeles, CA)
- …coordinate and/or implement increasingly complex research studies. Collects, evaluates and/or abstracts clinical research data . May assist in designing forms for ... data collection/abstraction. Enters and processes clinical research data into Electronic ...Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly with the Institutional… more
- CEDARS-SINAI (Beverly Hills, CA)
- …Administrator or Research Nurse to coordinate/implement study. Evaluates and abstracts clinical research data from source documents. Ensures compliance with ... research objectives. Completes Case Report Forms (CRFs). Enters clinical research data into Electronic Data...the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical… more
- Parexel (Montpelier, VT)
- …determines, and discusses with LSAD the correct timing and type of visits. + Performs Source Data Review (SDR), Case Report Form (CRF) review and Source ... + Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- CEDARS-SINAI (Beverly Hills, CA)
- …surpluses. Negotiates with sponsors the final payment due for account closeout. May conduct review and/or audits of clinical trial budgets. Serves as a resource ... analysis and clinical trial budget. Performs Medicare coverage analysis for clinical trials and collaborates with Institutional Review Board (IRB) to… more
- Christus Health (New Chapel Hill, TX)
- …per institutional protocol. Participates in the quality improvement and medication use review activities of the department. Collects data , conducts monitors and ... overseeing the preparation and dispensing of medications. Performs duties in the clinical areas assigned such as but not limited to anticoagulation clinics,… more
- Parexel (Columbia, SC)
- …determines and discusses with LSAD the correct timing and type of visits. + Performs Source Data Review (SDR), Case Report Form (CRF) review and Source ... + Follows quality issue processes by escalating systematic or serious quality issues, data privacy breaches, Clinical Study Protocol (CSP) or ICH-GCP compliance… more
- CEDARS-SINAI (Beverly Hills, CA)
- …Responsible for directing and managing a specified program within the clinical research operations unit, department, or division. Provides leadership, guidance and ... direction for the day-to-day clinical research operations and activities, including authority to make...May manage the research study intake process, including feasibility, review and endorsement and PRMC submission, as well as… more
- Teleflex (Minneapolis, MN)
- …completion of established project team goals and objectives, including study training and data review . - Facilitate corrective action assessment and maintain TMF ... to ensure materials are processed completely, based on accurate interpretation of clinical practice and data . TRAVEL REQUIRED: 50-75% (US and Internationally)… more
- CEDARS-SINAI (San Diego, CA)
- …agencies including the Food and Drug Administration (FDA and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) ... Job Description Come join our team! The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients… more
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