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Clinical Research Program Coordinator Jobs

Research Program Director Jobs
By Columbia University School of Nursing At New York City Metropolitan Area, United States
Experience with large-scale data management and research program and project management;
Working with the Principal Investigator and Project Manager to ensure compliance with all federal and university requirements;
Developing and implementing innovative study data management processes;
Managing project milestones in collaboration with the Principal Investigator and Project Manager;
Excellent organizational, interpersonal, and oral/written communication skills.
Leading efforts to obtain data on SDoH, store the data, and analyze the data as needed to disseminate the findings;
Clinical Research Coordinator - Seaver Center For Autism
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Translational Research Program Coordinator
By Alliance for Clinical Trials in Oncology At Boston, MA, United States
Working knowledge of clinical monitoring responsibilities and procedures.
Working knowledge of Clinical Trial Master File requirements.
Excellent oral and written communication skills and strong organizational abilities
Assist Project Manager in updating information on clinicaltrials.gov registry(ies) and other registries as necessary
2 – 4 years relevant biotech/pharma, and/or CRO. Prior lab experience required.
Advanced computer skills and ability to train others in system usage
Clinical Research Coordinator Jobs
By University of Louisville At Center, IN, United States
Maintain in-depth knowledge of protocol requirements and complete all required training prior to performing tasks.
Collect, document, and analyze data obtained from research studies.
Screen patients for entry into clinical studies and assess patients at each visit regarding compliance with protocol, complications, and difficulties.
Clinical Research Coordinator Ii-13400-043
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator Jobs
By ProSciento, Inc. At Chula Vista, CA, United States
Keeps the Clinical Trial Management System (CTMS) updated with pertinent information.
Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.
Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities.
Assists with data entry, as needed.
Communicates with study subjects regarding their study status and enrolment into the study.
Schedules subject appointments, performs subject reminder calls, and instructs subjects regarding any medication washout per protocol.
Clinical Research Coordinator Jobs
By Truvian At San Diego, CA, United States
Maintain working knowledge of multiple Institutional Review Boards (IRB) approved protocols and assist with data entry as needed
Clinical Site Management, including implementation of associated processes and documentations
Manage sign up calendar for available appointments for upcoming studies
Manage phlebotomist scheduling with external vendor
Record adverse events for donors experience in draw session
Maintain good record keeping of compensation log per donor and collaborate with Finance team to address pay out concerns
Clinical Research Coordinator Jobs
By Bozeman Health At Bozeman, MT, United States
Ability to adapt to change, manage uncertainty and possess exceptional time management skills
IRB Submission and regulator and regular document management
Source document creation, editing, and management
Participant tracking and contact log management
Dangerous Goods Shipping certification (within 30 days of Hire)
Good Clinical Practices/Human Subjects Research certifications (Within 7 days of Hire)
Clinical Research Coordinator Jobs
By Atlas Search At New York City Metropolitan Area, United States
Minimum of 1-3 years of relevant experience
Knowledgeable in clinical research protocols
Ensures protocol adherence and trains clinical staff on protocol-specific tasks.
Participates in tumor boards and other committees, as assigned.
Ensures accurate and complete submission of all study documentation, source documentation, and case report forms as required by study sponsors.
Indicates to billing department which patient visits and procedures are study related or not •
Clinical Research Coordinator Jobs
By Eurofins Lancaster Laboratories At Austin, TX, United States
Act as project manager on studies as directed by department manager
Provide a professional experience to test subjects, and answer all inquiries, as appropriate
Perform data entry and data review to ensure study quality
Efficiently time manage multiple projects
Succinctly communicate day to day project details to both department manager and Principal Investigator
Record observations, measurements, and test results, as required
Program Director - Ncri Clinical Research
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Strong leadership and management skills, including the ability to motivate
Excellent computer skills including extensive knowledge of MS Word, Outlook, Excel, PowerPoint, Teams.
Promote the clinical research environment, technical skills, and strategies to optimize clinical trial operations for ALS clinical trials.
Highly effective verbal and written communications skills.
Strong organizational skills, detail-oriented, and efficient.
Demonstrated experience in program development and oversight.
Program Director, Clinical Research Informatics - Clinical Research
By Keck Medical Center of USC At , Los Angeles, 90015, Ca $158,080 - $260,832 a year
Program Planning and Management - Plans and develops CRI objectives and content. Identify trends and research needs and establish priorities accordingly.
Identify technical education opportunities to enhance user experience.
Develops and manages program budgets and recommends or makes budgetary and resource allocations. Provides financial status reports as requested.
Ensures all information systems products meet standards and user requirements. Tests software and hardware and monitors and resolves problems.
Advises leadership regarding Informatics systems requirements. Facilitates planning and directs the design, installation, modification, and operations of research information systems.
Reviews and prioritizes systems development requests. Prepares cost estimates for current and proposed projects, reflecting staff and equipment requirements.
Program Coordinator And Research Assistant
By CSIS Southeast Asia Program At Washington, DC, United States
• Assist with outreach activities and contacts management
• Manage the publication process for reports and other digital products
• Draft contracts and manage expenses including payment to consultants/associates.
The minimum salary for this position is $55,000.
Essential functions may include, but are not limited to the followingAdministrative (70%)
• Maintain Southeast Asia Program calendars, correspondence, and travel itineraries
Program Coordinator And Research Assistant-Southeast Asia Program
By Center for Strategic and International Studies (CSIS) At Washington, DC, United States
Program management, budget, and event planning experience highly preferred.
Assist with outreach activities and contacts management
Manage the publication process for reports and other digital products
Draft contracts and manage expenses including payment to consultants/associates.
Knowledge of Southeast Asian political, security, and/or economic issues desired.
1-2 years of professional experience preferred.
Clinical Research Consortia Coordinator-Remote
By UC San Diego Health At , San Diego, 92103, Ca $29.99 - $48.25 an hour
Experience with data management tools such as REDCap.
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word.
Experience interpreting medical charts, experience in abstracting data from medical records.
Experience with clinical trials participant or study subject recruitment.
Experience coordinating study startup activities.
Experience providing in-service training to various research personnel on protocols, processes, and procedures.
Clinical Research Coordinator Jobs
By CRO Strategies At Miami, FL, United States
Overseeing the smooth running of clinical trials.
Collecting, coding, and analyzing data obtained from research.
Informing participants about study objectives.
Monitoring research participants to ensure adherence to study rules.
Adhering to research regulatory standards.
Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
Clinical Research Coordinator - Chicago
By The IMA Group At Chicago, IL, United States
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
Additional duties and responsibilities may be assigned as needed.
Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
Ops Clinical Research Coordinator
By University of Florida At , , Fl $24.90 - $29.69 an hour
Works with the PI/ research manager(s) to develop and implement recruitment strategies in accordance with IRB requirements and approvals.
Works with the PI/lead coordinator(s) to manage the day-to-day activities of the study including problem solving, communication and protocol management.
Clinical-trials management systems and survey tools such as Qualtrics
Assists the PI and research managers(s) in reviewing protocols
Collaborates with the research manager(s) to prepare a categorized budget and justification.
Collaborates with the PI and research manager(s) to prepare IRB and any other regulatory submission documents as required by the protocol.
Clinical Research Coordinator Jobs
By Intellectt Inc At Charlotte, NC, United States

Title: Clinical Research Coordinator Duration: 2 Years Location: Charlotte, NC Job Summary The Clinical Research Coordinator will be an essential team member in active clinical research, ...

Clinical Program Nurse Coordinator Iii
By Sutter Health At , San Francisco, Ca $80.50 - $106.26 an hour
Equivalent experience will be accepted in lieu of the required degree or diploma.
DEPARTMENT SPECIFIC CERTIFICATION & LICENSURE
Sutter Health is an equal opportunity employer EOE/M/F/Disability/Veterans.