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Clinical Research Program Coordinator Jobs in Dallas, Texas

Research Program Coordinator Jobs
By Parkland Health At Dallas, TX, United States
Experience working in clinical research, preferably as a clinical research coordinator/manager, including research consenting and management of protocol requirements preferred.
Strong analytic and computer skills in addition to knowledge of word processing, database management and spreadsheet software.
Experience working with data collection, database management, and preparation of research reports preferred. Experience designing research data collection tools preferred.
Additional experience with patient care or clinical research may substitute for the minimum education requirement.
Knowledge of SPSS, RedCap and/or other database management and analytics software preferred.
Six (6) years of experience working with patient care processes, as a clinician, researcher or professional in a clinical support service.
Clinical Research Coordinator 1 Jobs
By Baylor Scott & White Health At , Dallas, 75226, Tx
Implements various protocols for assigned research projects with appropriate departments throughout the organization by interacting with PIs, clinical managers and supervisors.
Obtains knowledge of departmental functions through reading literature, attending workshops, seminars and conferences and participating in professional organizations.
Research certification or other certifications per specialty area preferred.
Proven written and oral communication skills.
Exceptional computer skills, including Microsoft Office.
Ability to manage time reactive projects in order to meet deadlines.
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.
Clinical Research Coordinator Jobs
By New England Baptist Hospital At , Boston, 02120, Ma

When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Job Type: Regular Scheduled Hours: 40 Work Shift: Day (United States ...

Coordinator, Clinical Studies - Translational Research Training Program
By MD Anderson Cancer Center At , Houston, 77030, Tx
Follows patients on study and maintains knowledge of adverse events
Collaborates with physicians, mid-level practitioners, research nurse and data managers to document patient care
Coordinates reports for the study manager for submitting grant data in a timely manner
Provides study related coordination including protocol maintenance
Develops and maintains a processing and tracking system for all protocol related documents
Develops patient care methodology for protocols, including criteria for patient participation
Clinical Research Coordinator - Cantor Center
By Dana-Farber Cancer Institute At , Boston, 02215, Ma

Job ID: 34839 Location: 450 Brookline Ave, Boston, MA 02215 Category: Clinical Research Employment Type: Full time Work Location: PTL Remote: 2-3 days remote/wk Overview The Clinical ...

Coordinator, Clinical Research Program - Leukemia
By MD Anderson Cancer Center At , Houston, 77030, Tx
Systematically review and report on individual faculty assistant compliance with protocol-related job duties
Develops and maintains a processing and tracking system for all protocol related paperwork
Establishes and participates in information systems for the development of research programs including writing, processing, submission and maintenance of protocols
Provides protocol and protocol-related data and information for grant applications in collaboration within the department
Undertake and oversee clinical trial-related grant applications through public and private sector mechanisms
Collaborate on larger departmental grant applications as preparation and production specialist
Clinical Research Coordinator Jobs
By HCA Healthcare At Fort Worth, TX, United States
Education assistance (tuition, student loan, certification support, dependent scholarships)
Family support through fertility and family building benefits with Progyny and adoption assistance.
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.
You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance
You will ensure timely adherence to protocol requirements
You will communicate all protocol-related issues to appropriate study colleagues or manager
Research Program - Manager
By Leidos At , San Antonio, 78205, Tx $66,300 - $137,700 a year
Assist Government personnel in initiating and maintaining regular IACUC/IRB requirements.
Experience in a military medical research laboratory.
Due to Federal contract requirements, U.S. citizenship is required.
Manager for the research program
Facilitate information flow between program members, scientific directors, and the Command.
Assist the Government with gathering information for research program taskers.
Program Coordinator - Epidemiology Research
By Mayo Clinic At , Rochester, 55905, Mn $52,874 - $78,832 a year

Additional Qualifications: Prior experience with genomic data, genetic result disclosure, and/or genetic counseling preferred.

Affirmative Action and Equal Opportunity Employer

Clinical Research Coordinator Jobs
By Dana-Farber Cancer Institute At , Boston, 02215, Ma

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:

Clinical Research Coordinator 1 Jobs
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Strong organizational and time management skills
. Bachelor’s degree, with an academic record demonstrating experience and skills in analytical thinking and/or quantitative methods
Strong communication skills including proficiency in written and spoken English
Ability to work both independently and as part of a team, and to collaborate with team members located remotely
Participate in all phases of research projects, from conception and design of studies through proofing manuscripts for submission to academic journals
Monitor study activities for compliance with all applicable regulations and facilitate trainings for study personnel as needed
Clinical Research Coordinator Jobs
By SBR Scientific At Plano, TX, United States
Ability to work autonomously, remotely, in dynamic fast-paced environments, using problem solving skills to adapt to changing demands.
Excellent interpersonal skills, openness to feedback, and a desire to learn and improve skills.
BS, MS, MD, nursing degree or relevant clinical research experience in a related discipline
1-3 years of clinical research experience preferred
·Maintain constant communication with Principal Investigator and Research Manager regarding patient care issues.
Basic understanding of statistical data analysis and interpretation.
Clinical Research Coordinator Jobs
By RAOOF MD Dermatology At , Encino, 91436, Ca

Facilitate and coordinate the daily clinical trial activities. Responsible for recruitment, patient screening, and enrollment for clinical studies. Schedule and attend study participant ...

Clinical Research Coordinator Jobs
By Piedmont Healthcare At , Atlanta, Ga

Forbes named Piedmont one of Georgia’s 10 best employers and the highest-ranked healthcare provider.

Clinical Research Coordinator Jobs
By Vitalief Inc. At Bryan, TX, United States
Any exposure to EPIC (Electronic Health Records system) and/or OnCore (Clinical Trials Management System) is a plus.
Manage eligibility check lists, perform patient screening/consenting (informed consent), patient activation and managing patient care (patient retention).
Any experience in Oncology and/or working on complex clinical trials is a plus.
Must possess excellent interpersonal skills to interact with patients in a clear and confident manner.
Experience in preparation of documents for submission to the Institutional Review Board (IRB), continuing reviews, and submission of amendments and modifications.
Must have strong Microsoft Office skills.
Clinical Research Coordinator - Houston
By Healthwaze At Bellaire, TX, United States
Manages the inventory of equipment and supplies related to the study.
Responsible for ensuring study compliance with local and federal laws and regulations.
Facilitate regulatory start up-documentation and filings, including central IRB submissions.
Recruits and prescreens potential study participants and may perform intake assessments.
Schedule and coordinate protocol-specified study visits.
Creates and/or maintains all documents and records related to the study.
Clinical Addiction Research & Education Program Assistant
By Boston Medical Center At , Boston, 02118, Ma
Calendar management including scheduling and preparing materials
Bachelor's Degree (or equivalent combination of formal education and experience) required.
Some experience in research settings
Experience with Microsoft Office including Excel, Word, PowerPoint, and Outlook
Position: Clinical Addiction Research & Education Program Assistant
Arranging travel for key program staff and submitting travel reimbursements
Clinical Research Coordinator Jobs
By Massachusetts General Hospital(MGH) At , Boston, 02114, Ma
Strong organizational and time management skills required
Working knowledge of statistics, SPSS, and data management programs desired
Perform clerical/organizational work, quality control, and budget management, if needed
Manage and prioritize multiple projects simultaneously
Data entry and quality control procedures
Adhere strictly to all Institutional Review Board (IRB) guidelines and confidentiality requirements