- Consistently demonstrates adherence to the standards for the responsible conduct of research.
- Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
- Stays informed of and adheres to institutional policies and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information.
- Uses research funds and resources appropriately.
- Maintains confidentiality of data as required.
- Meets all annual job-related training and compliance requirements.
- Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
- Accurately creates, completes, maintains and organizes study documents.
- Accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.
- Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.
- Reviews current literature to obtain information relevant to clinical research program, as directed.
- Attends study meetings, which could include overnight travel, as requested by principal investigator.
- Works well with other members of the research team and seeks and provides input when appropriate.
- Serves as an effective liaison between the investigators, sponsors, hospital departments involved with research studies and the Clinical Research Center.
- Employs strategies to recruit and retain research participants, while adhering to the IRB-approved recruitment plan.
- Screens subjects for eligibility per the protocol and institutional policies.
- Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.
- Independently coordinates, conducts and documents visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and SOPs for minimal risk studies or for other studies under direction.
- Interacts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.
- Engages participants/LARs in the informed consent process according to institutional policies.
- Follows procedures for documentation of study payments and participation incentives.
- Plans, conducts and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.
- Ensures regulatory integrity of protocols through the accurate and timely preparation and submission of documents and reports to the sponsor, IRB and other oversight bodies in accordance with federal regulations, sponsor SOPs and institutional policies.
- Collects, prepares, processes, ships and maintains accurate inventory of research specimens, and trains others in performing these tasks.
- Suggests improvements to specimen handling processes, when needed.
- Authors study documents, including informed consents, protocol-specific source documents and IRB contingency responses.
- Registers and records participant visits in the appropriate tracking system.
- Anticipates study needs and subject caseload in order to meet organizational objectives and deadlines in a timely manner.
- Coordinates, prepares for and responds to routine oversight body visits and audits.
- Performs query resolution and assists with addressing and correcting audit findings.
- Collects data from patient medical records, interviews, questionnaires, diagnostic tests and other sources.
- Ensures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate and Complete).
- Ensures that queries are resolved within sponsor and institutional timelines.
- Plans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.
- Ensures secure storage of study documents.
- Anticipate and responds to customer needs; follows up until needs are met
- Demonstrate collaborative and respectful behavior
- Partner with all team members to achieve goals
- Receptive to others' ideas and opinions
- Contribute to a positive work environment
- Demonstrate flexibility and willingness to change
- Identify opportunities to improve clinical and administrative processes
- Make appropriate decisions, using sound judgment
- Use resources efficiently
- Search for less costly ways of doing things
- Speak up when team members appear to exhibit unsafe behavior or performance
- Continuously validate and verify information needed for decision making or documentation
- Stop in the face of uncertainty and takes time to resolve the situation
- Demonstrate accurate, clear and timely verbal and written communication
- Actively promote safety for patients, families, visitors and co-workers
- Attend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance
-
Research Coordinator
2 weeks ago
University of Maryland College Park, United States**Posting Details**: · - Posting Details**Position Number**: · **Title**: · - Coordinator**Functional Title**: · - Research Coordinator**Category Status**: · - 33-Exempt Regular**Applicant Search Category**: · - Staff**University Authorized FTE**: · - 1.000**Unit**: · - CMNS-Eart ...
-
Research Coordinator
1 week ago
Air-Conditioning, Heating, and Refrigeration Institute Arlington, United StatesThe Research Coordinator is responsible for performing complex administrative and managerial functions that require the use of independent judgment and discretion. This position will provide primary support to the Vice President of Research and interact with heating, ventilation, ...
-
Research Coordinator
2 days ago
University of Maryland College Park, United States**Posting Details**: · - Posting Details**Position Number**: · **Title**: · - Research Coordinator**Functional Title**: · - Research Coordinator**Category Status**: · - 33-Exempt Regular**Applicant Search Category**: · - Staff**University Authorized FTE**: · - 100**Unit**: · - CM ...
-
Research Coordinator
2 days ago
AHRI Arlington, United StatesEnsuring human comfort, productivity, and safety, while practicing environmental stewardship is the mission of the Air-Conditioning, Heating, and Refrigeration Institute (AHRI). Our 300+ member companies produce more than 90 percent of the residential and commercial air condition ...
-
Clinical Research Coordinator
1 week ago
Children's National Medical Center Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Clinical Research Coordinator
3 weeks ago
Children's National Hospital Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Biomedical Research Coordinator
1 week ago
Kelly Services, Inc. Rockville, United StatesKelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Kelly Government Solutions offers administrative, IT, engineering Research Coordinator, Medical ...
-
Clinical Research Coordinator
1 week ago
Children's National Hospital Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Clinical Research Coordinator
1 week ago
Children's National Medical Center Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Clinical Research Coordinator
1 week ago
Children's National Medical Center Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Clinical Research Coordinator
1 week ago
Quadrant Inc Rockville, United StatesJob ID: · Clinical Research Coordinator · Rockville, MD · MUST: · 1 plus years of experience in the clinical research field · Experience with data collection · Experience with patient enrollment and screening · Experience evaluating data · Experience working with investigators · ...
-
Clinical Research Coordinator
2 weeks ago
Children's National Health System Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, docume Clinical Research, Research C ...
-
Clinical Research Coordinator
3 weeks ago
IQVIA, Inc. Rockville, United StatesJob Overview: · Work as an integral member of investigator site staff managing the day-to-day coordination and execution of clinical studies in accordance with the protocol, contracted scope of work, good clinical practice, sponsor and Avacare standard operating procedures (SOPs) ...
-
Clinical Research Coordinator
3 days ago
Quadrant Rockville, United StatesClinical Research Coordinator · Rockville, MD · MUST: · 1 plus years of experience in the clinical research field · Experience with data collection · Experience with patient enrollment and screening · Experience evaluating data · Experience working with investigators · Experience ...
-
Clinical Research Coordinator
4 weeks ago
Cape Fox Corporation Rockville, United StatesShare this job as a link in your status update to LinkedIn. · Job Title · Clinical Research Coordinator, · Job Description · Concentric Methods is seeking a Clinical Research Coordinator to join our team in Rockville, MD in support of the NIH. · Responsibilities: · Supports clini ...
-
Clinical Research Coordinator
1 week ago
Sunstone Therapies Rockville, United StatesJob Description · Job Description · Scope: · We are seeking a highly skilled and motivated Clinical Research Coordinator who is also a certified Registered Nurse (RN) to join our team in Rockville, MD. The successful candidate will be responsible for coordinating and overseein ...
-
Clinical Research Coordinator
1 week ago
Children's National Hospital Rockville, United StatesThe Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinic ...
-
Clinical Research Coordinator
1 week ago
Sunstone Therapies Rockville, United StatesJob Description · Job DescriptionScope: We are seeking a highly skilled and motivated Clinical Research Coordinator who is also a certified Registered Nurse (RN) to join our team in Rockville, MD. The successful candidate will be responsible for coordinating and overseeing clinic ...
-
Clinical Research Coordinator
1 week ago
Specialist Office Rockville, United StatesJob Description · Job DescriptionClinical Research Coordinator · Rockville, MD · MUST: · 1 plus years of experience in the clinical research field · Experience with data collection · Experience with patient enrollment and screening · Experience evaluating data · Experience workin ...
-
Clinical Research Coordinator
1 week ago
Children's National Rockville, United States Full timeClinical Research Coordinator AD) Description The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, c ...
Clinical Research Coordinator - Rockville, United States - Children's National
Description
Clinical Research Coordinator Description The Clinical Research Coordinator participates in or leads day-to-day operations of clinical research studies conducted by a principal investigator. The Research Coordinator performs a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations. This position may direct the work of junior staff, train personnel and direct the work of a Clinical Research Assistant as assigned. Qualifications Minimum Education
Bachelor's Degree B.A./B.S. degree in a science, technical, health-related field or other applicable discipline (Required)
Minimum Work Experience
1 year 1 year of applicable work, research or internship experience (e.g. research assistant, data manager, clinician or other interaction with a research population). (Required)
Functional Accountabilities
Responsible Conduct of Research
Research Administration
Participant Enrollment
Study Management
Data Collection
Teamwork/Communication
Performance Improvement/Problem-solving
Cost Management/Financial Responsibility
Safety
Primary Location
:Maryland-RockvilleWork Locations
:Neuropsych Montgomery County15245 Shady GroveSuite 350 South BuildingRockville20850Job
:ResearchOrganization
:Ctr Neuroscience & Behav MedPosition Status:R (Regular)-FT - Full-TimeShift:DayWork Schedule:8:30-5:00Job Posting
:May 10, 2024, 3:02:15 PM