Clinical Research Coordinator

Location
Bethesda, Maryland
Posted
May 12, 2022
Ref
2022-11872
Hotbed
BioCapital
Required Education
Bachelors Degree
Position Type
Full time

We are currently searching for a Clinical Research Coordinator to provide support services to satisfy the overall operational objectives of the Eunice Kennedy Shriver National Institute of Child Health and Human Development. The primary objective is to provide services and deliverables through performance of support services.  This opportunity is full-time, and it is on site in Bethesda, MD.

 

Duties & Responsibilities
  • Coordinate clinical admissions for research protocols This will include contact with families’ patients, initial discussions of the clinical protocol with patient family guardian, arranging travel, scheduling, and coordinating subspecialty appointments, coordinating admissions data collection clinical and research samples, coordinating with patient parent for release of pertinent medical records to the protocol team at NICHD
  • 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
  • Monitor electronic medical record system to ensure necessary components are present and complete such as data collection forms, progress notes, participant information forms and diagnostic test completion forms
  • Liaison between the study subjects and the investigators concerning any problems or adverse events including out of range vitals, etc.
  • Interact with patients, parents, families, nursing staff, physician staff, social worker staff, clerical staff, laboratory staff, and other clinical center professionals
  • Serve as an associate investigator on protocols and obtain informed consent from patient parent legal guardian
  • Coordinate and maintain research records in accordance with NIH guidelines
  • Review patient care orders in CRIS for accuracy and contact the appropriate clinical fellow for any problems identified
  • Review laboratory and clinical test results and report results to the attending physicians
  • Participate in relevant clinical rounds
  • Provide continuity of care to patients enrolled on assigned protocols
  • Serve as a resource to patients and families enrolled in research protocols; facilitate communication with referring physician health care provider
  • Communicate with the IRB annual reviews of the protocol; assist principal investigators on all matters that relate to communications with the IRB and the Office of the Clinical Director
  • Assist clinical and research staff to ensure that Case Report Forms (CRFs) are completed and document changes in research participant condition, adverse events, concomitant medication use, protocol compliance, response to study drug, and other required fields
  • Assist researchers with study testing, observations data entry and other duties associated with study sessions
  • Assist staff to develop, assemble related documentation, and maintain regulatory binders for all protocols
  • Assist researchers to develop, maintain and complete study data collection forms and source documents
  • Prepare patient charts for clinic days and provide initial or follow-up assessment forms, patient labels, most recent medication lists and lab and procedure printouts
  • Assist staff screen prospective study subjects and participate in scheduling participants for research visits and procedures
  • Schedule and coordinate outpatient and inpatient visits, diagnostic studies, and medical tests
  • Update and maintain logs and records of patient and family contacts
  • Assist protocol staff submit initial applications, amendments, continuing reviews, Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines

 

#SOAR

 

#LI-JR1

Requirements

 

Qualifications:

  • Ph.D. in Life Sciences, Biology, General Medical and Health Services or a related discipline is preferred, but not required
  • Bachelor’s degree in Biology or General Medical & Health Services, minimum requirement
  • At least 3 years of related experience

 

Skills:

  • Strong communication skills, both oral and written
  • MS Office Suite

 

Company Description

Dovel Technologies and its Family of Companies (Medical Science & Computing and Ace Info Solutions) was acquired in October 2021.

 

Guidehouse is a leading global provider of consulting services to the public sector and commercial markets, with broad capabilities in management, technology, and risk consulting. By combining our public and private sector expertise, we help clients address their most complex challenges and navigate significant regulatory pressures focusing on transformational change, business resiliency, and technology-driven innovation. Across a range of advisory, consulting, outsourcing, and digital services, we create scalable, innovative solutions that help our clients outwit complexity and position them for future growth and success. The company has more than 12,000 professionals in over 50 locations globally. Guidehouse is a Veritas Capital portfolio company, led by seasoned professionals with proven and diverse expertise in traditional and emerging technologies, markets, and agenda-setting issues driving national and global economies.

 

Guidehouse is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation.

 

Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance, including the Fair Chance Ordinance of Los Angeles and San Francisco.

 

If you have visited our website for information about employment opportunities or to apply for a position, and you require accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.

 

Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse, and Guidehouse will not be obligated to pay a placement fee.