Clinical Research Coordinator - NIH - Start Now

We are looking to hire a driven Clinical Research Coordinator - NIH to join our diverse team at Kelly Services in Bethesda, MD.
Growing your career as a Full Time Clinical Research Coordinator - NIH is an awesome opportunity to develop productive skills.
If you are strong in cooperation, adaptability and have the right initiative for the job, then apply for the position of Clinical Research Coordinator - NIH at Kelly Services today!

Kelly 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, scientific, and healthcare professionals the opportunity to work with one of the most prestigious research organizations in the world. We are currently seeking a Clinical Research Coordinator with the National Institutes of Health in Rockville, Maryland.

This is a long-term contract position which offers:

• Competitive salary with comprehensive benefit package

• Opportunity to work at NIH, the world's foremost medical research center

• Learn more about what Kelly can do for you at

OBJECTIVE:

The primary responsibilities

for this on-site Clinical Research Coordinator (CRC) position will be to

provide clinical and biospecimen research coordination for the TIU and

affiliated programs.

TASKS:

• Supports clinical staff develop, implement and maintain clinical research data files and materials.

• Supports clinical staff develop, implement and maintain clinical research data files and materials.

• Collects research data and prepares information for inputs and analysis.

• Supports the development of forms and questionnaires.

• Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.

• Collects research data and prepares information for inputs and analysis.

• Monitors subject's progress and reports adverse events. Supports assembly, development and review of new research projects. Supports the creation and management of clinical websites and web-based tools.

• Assist in development of general plans for collection, storage, and analysis of clinical and biospecimen research data

• Assist in development of biospecimen records management protocols and systems . Assist with regular biospecimen pick up, transport, logging, shipping, and receiving

• Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry

• Supports the development of forms and questionnaires.

• Supports the development of Redcap databases, surveys, and questionnaires

• Work with investigators to draft and submit protocol packages, actions, and applications to IRB using the designated protocol tracking and management databases system(s)

• Assist clinical and research staff to ensure that study and regulatory forms are completed and submitted on time to IRB and regulatory bodies

• Document changes in research participant condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and other required fields on Case Report Forms

• Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.

• Reporting of adverse events to IRB and regulatory bodies

• Monitors subject's progress and reports adverse events.

• Assist staff writing and editing surveys/questionnaires for participants, providers, families, and collaborators

• Supports assembly, development and review of new research projects.

• Assist with scheduling and coordinating outpatient and inpatient visits, diagnostic studies and medical tests

• Supports the creation and management of clinical websites and web-based tools.

• Assess study protocols and studies for regulatory compliance, adherence to IRB approvals and Federal standards, such as HIPAA, human subject ethics, privacy, etc. and generate quality assurance reports

• Organizes and performs clinical research, utilizing internet and other available clinical resources.

• Respond to and document verbal and written inquiries from patients, patient families, providers, outside research investigators, and the general public

• Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.

• Assist in preparation of accurate source documents related to all research procedures and submitting these for timely review

• Supports clinical staff develop, implement and maintain clinical research data files and materials.

• Review collaborator/participating organization IRBs for consistency with NIH policies . Assist with development/review of data capture forms to facilitate seamless entry into databases

• Work with NIMH information technology to establish and implement research databases (e.g. Redcap) and spreadsheets

• Retrieve and log research-related information from medical records, hospital information system and laboratory information system

• Schedule and participate in monitoring and auditing activities and coordinate responses to audits

• Develops and facilitates training to new research coordinators and mentors researchers in Good Clinical Practices.

• Create and update protocol standard operating procedures (SOPs) as needed. Participate in developing recruitment materials with input of PIs and IRB approval for referral sources outlining eligibility information

• Performs and or coordinates outreach activities, as appropriate, to meet research recruitment and enrollment goals.

• Assist with new clinical research coordinators on all aspects of research support

REQUIREMENTS. The contractor must have:

Field of Study

• Cognitive Science and Biopsychology

Software

• RedCap

Skills

• Liaising with regulatory authorities - Previous clinical trial work

When you apply, please know a Kelly Government Solutions Recruiter will review your resume and will contact you directly, if your skills and experience match the requirements of this position.

Due to the high volume of inquiries, we regret that we cannot accept phone calls. Even if you aren’t contacted for this position, you are still part of our talent network. All Kelly recruiters have access to your profile, which expands your opportunities even further.

As a specialty talent company, Kelly is committed to doing the right thing for our talent and clients. We stand up for equity, inclusion, fair treatment, and opportunity for all as these build the foundation of our Talent Promise. With a focus on safety, value, well-being, investment, and opportunity, Kelly’s Talent Promise confirms our commitment to those in search of a better way to work and live and to help discover what’s next.

It is obvious things are different than they were just a few months ago. Kelly is at the forefront of ensuring the safety of our employees in this new working environment. Be well and stay strong.

You should know: Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.

Benefits of working as a Clinical Research Coordinator - NIH in Bethesda, MD:

● Excellent benefits
● Opportunities to grow
● Competitive salary