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Clinical Research Organization Jobs

829 matches | 1 - 20 displayed
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date  location  job detail
Mar 21,2019 USA-MA-Cambridge Senior Epidemiologist
\u003Cp\u003E\u003Cb\u003EResponsibilities: \u003C/b\u003E\u003C/p\u003E\u003Cul\u003E\n\u003Cli\u003EPrimary liaison between the assigned Therapeutic Area and key stakeholders to ensure translation of the Clinical Development Plan into observational research deliverables. Actively participates t
Mar 20,2019 USA-FL-Tampa Homecare Clinical Operations Specialist - Registered Nurse (RN)
Position Description:
The Clinical Operations Specialist is responsible for the agreed-upon clinical activities that help facilitate
and improve the day-to-day clinical operations within an office. The position will be multi-functional that
focuses on overall clinical and operational coordination an
Mar 21,2019 USA-CA-Inglewood Telecommute Clinical Research Associate - Inglewood
A contract research organization is in need of a Telecommute Clinical Research Associate.Candidates will be responsible for the following: Conducting study site visitsEnsuring proper storage of all investigational productServing as mentor/trainer for CRAsQualifications for this position include:Abil
Mar 20,2019 USA-MA-Andover Clinical Project Manager
Job Description
Clinical Project Manager
Responsibilities
Schedule and review project tasks, providing leadership in the delivery of services to clients and ensuring staff fulfills their responsibilities in accordance with client's policies, procedures, SOPs, ICH-GCPs, and country specific regulator
Dec 31,1969 USA-MA-Cambridge Executive Administrative Assistant IV
Assist in the administration of the Compliance Department, including setting up domestic and international travel, expense tracking, coordinating and setting up internal and external meetings, ensuring a smooth and efficient flow of day-to-day operations.
Complex calendar and meeting planning, inclu
Mar 21,2019 USA-NM-Gallup Clinical Care Specialist\/Staff Nurse RN
Loyal Source Government Services is looking for a qualified Staff Development Registered Nurse to work with the Gallup IHS in New Mexico as a civilian contractor promoting and restoring patients? health.\n\nOur employees are our greatest asset! Benefits to working with Loyal Source include but are
Dec 31,1969 USA-MA-Boston R&D Project Coordinator
Assists Global Project Manager in maintaining MSP planning and reporting for assigned projects
Coordinates administrative type project management activities such as team lists and SharePoint maintenance
Details:
The pay range we're offering is
66 - 66
This position may present an opportunity to go p
Dec 31,1969 USA-CT-Meriden Manufacturing Technician II
Operates general manufacturing equipment in strict accordance with SOPs.
Maintains all associated documentation for operations being performed.
Reviews and records physical inventory of stock items.
Tasks to be completed may include protein purification, solvent extractions, tissue culture, preparat
Mar 15,2019 USA-CA-South San Francisco Study Data Manager I
This is an excellent opportunity to start a career with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients' lives! 
This is an excellent opportunity to start a career with one of the largest Biopharmaceutical companies in t
Mar 20,2019 USA-CA-San Francisco Clinical Trial Associate
\u003Cp\u003E\u003Cb\u003EResponsibilities: \u003C/b\u003E\u003Cbr\u003E\u2022 Monitoring Visit Report Review \u003Cbr\u003E\u2022 Informed Consent Review \u003Cbr\u003E\u2022 IP Reconciliation (Endpoint a plus but not required) \u003Cbr\u003E\u2022 Oversee TMF Quality Review for study team \u003Cbr
Mar 21,2019 USA-CA-South San Francisco Clinical Trial Associate
Supports the logistical aspects of clinical trial conduct in compliance with Good Clinical Practice (GCP) and relevant Standard Operating Procedures (SOPs).
Works closely with members of the Clinical Team, specifically in activities of study set-up, conduct and completion of clinical studies.
Assist
Dec 31,1969 USA-CT-Ridgefield Scientist II
Manage patient samples coordination, biobanking, tracking and organization.
Conduct cellular isolation and culture of human PBMCs, B and T cells, ELISA and RNA extraction .
Details:
The pay range we're offering is
28 - 30
This position may present an opportunity to go permanent.
Our Client:
Our clie
Mar 21,2019 USA-MA-Cambridge Research Associate
Interpret data with support from supervisor and contribute to technical reports.
Initiate workflows for protocol and report uploads/approvals in relevant electronic documentation systems.
Plan and execute formulation of screening stability experiments.
Details:
The pay range we're offering is
25 - 2
Dec 31,1969 USA-NJ-Madison Principal Standards Analyst
Review and understand new SDTM IGs, as well as TAUGs and Standard Controlled Terminology.
Review SDTM mappings, acrf.pdf annotations, csdrg.pdf and define.xml.
Details:
The pay range we're offering is
45 - 65
This position may present an opportunity to go permanent.
Our Client:
Our client is an awar
Dec 31,1969 USA-CA-South San Francisco Clinical Systems Analyst
Perform system upgrades and providing system maintenance whenever necessary.
Participate in developing policies and creating training tools for Data Management systems users.
Details:
The pay range we're offering is
70 - 110
This position may present an opportunity to go permanent.
Our Client:
Our c
Dec 31,1969 USA-NJ-Ridgefield Project Manager I
Determine project scope
Use of lean/FMEA/statistical and other methods to perform preliminary options analysis, change control development and execution, commissioning and qualification documentation
Development and execution
Validation documentation development and execution, project tracking and c
Dec 31,1969 USA-NJ-Woodcliff Lake Contract Recruiter
Manages personnel requisitions, conducts a needs assessment with hiring manager, resume reviewing & tracking, creates job postings & oversees the posting process.
Conducts phone screens and 1st interviews.
Confers with senior leadership to identify personnel needs, workforce planning strategies and
Mar 21,2019 USA-IL-North Chicago Medical Writing Word Processing Coordinator
Processes, proofreads, verifies and manages various clinical regulatory documents, ensuring they are submission-ready for publishing with an appropriate level of accuracy and consistency.
Communicates regularly with colleagues and management regarding timelines and conflict to timelines for word
Dec 31,1969 USA-MA-Cambridge Clinical Regulatory Coordinator
Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory authorities
Maintain Trial Master Files
Act as a liaison between the Site IRBs and Clinical team to resolve regulatory queries and concerns.
Details:
The pay range we're offering is
45 - 50
This positio
Dec 31,1969 USA-IL-North Chicago Clinical Medical Services Specialist II
Identify and collect adverse event information and complete the in-take of a Pharmacovigilance safety report in the client's system
Respond to medical information requests using approved resources and document in the medical information system
Identify product quality and device complaints and docu
829 matches | 1 - 20 displayed
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