57 clinical research coordinator entry level jobs at 13 companies in Redland, MD
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Clinical Research Coordinator (Otolaryngology)
Baltimore, Maryland, United States
$17-$30/hrOnsiteFull Time
Johns Hopkins University School of Medicine: Private nonprofit medical school serving students, scientists, physicians, and patients through education, research, and clinical care.
Bachelor's degree in a related field required; experience in human subjects research preferred. Duties include study coordination, recruitment, consenting, data entry, IRB submissions.
Georgetown University Medical Center: Catholic academic health and science center training health professionals and scientists through research, teaching, and patient care.
2+ YOEManage and coordinate multiple clinical trials, conduct study visits, ensure protocol adherence, regulatory maintenance, timely data entry and adverse event reporting, and coordination with ancillary departments.
Guidehouse: Global consulting firm serving public and commercial sectors.
1+ YOEBachelor’s in nursing/health sciences/public health/clinical research,1+ year supporting clinical trials,oncology trial experience preferred,knowledge of FDA/ICH-GCP,human subjects protection,EMR/CTMS/EDC experience,and ability to obtain public trust.
Electronic Medical Records (EMR), clinical trial management systems, electronic data capture platforms
SuccessFactors Recruiting: Clinical Research Coordinator (Nephrology) (121786)
Baltimore, Maryland, United States
$17-$30/hrOnsiteFull Time
Johns Hopkins University School of Medicine: Private nonprofit medical school serving students, scientists, physicians, and patients through education, research, and clinical care.
Coordinate clinical research activities, manage protocol implementation, obtain consent, interact with participants, assist with IRB submissions, and perform study data entry. Bachelor's degree required; related research experience preferred.
CenExel CBH: Private U.S. clinical research site network conducting complex trials for pharmaceutical, biotechnology, and CRO partners.
0+ YOEAssist coordinating clinical trials per ICH/GCP and protocol; document events; perform assessments (vitals, EKGs, blood draws); communicate with sponsors; 0-3 years medical experience; high school required, bachelor's preferred.
Concentric Methods: Alaska Native-owned federal contractor delivering medical, information technology, administrative, biosafety, and engineering services to government clients.
2+ YOEBachelor's degree, 2 years related experience, proficiency in data collection, EMR/analysis workflows, strong communication, organization, and familiarity with STATA and NVivo.
Inova: Nonprofit healthcare provider based in Northern Virginia.
2+ YOEAssociate's degree or relevant experience in lieu of degree required; 2 years regulatory coordination and site-based clinical research experience preferred. SOCRA or ACRP certification preferred.
Kennedy Krieger Institute: Independent nonprofit medical, educational, research, and community-services organization serving children and adults with neurological and developmental conditions.
2+ YOEBachelor’s degree required, preferably in a related scientific field, plus at least 2 years of research-related work experience.
Kennedy Krieger Institute: Independent nonprofit medical, educational, research, and community-services organization serving children and adults with neurological and developmental conditions.
2+ YOEBachelor’s degree required, preferably in a related scientific or behavioral field, plus at least two years of research-related work experience.
AARA Clinical Research: A rheumatology practice conducting and coordinating clinical research across multiple sites.
1+ YOEBachelor's degree, 1 year CRC experience, knowledge of ICH-GCP and federal clinical research regulations, strong organization/communication, ability to lift 20 lbs, and willingness to travel to nearby sites.
Clinical Research Coordinator I - Bilingual (Spanish)
Laurel, Maryland, United States
OnsiteFull Time
ObjectiveHealth: Integrated clinical research provider helping physicians and healthcare organizations bring clinical trials into patient care.
Certification such as MA or phlebotomy required; experience conducting IRB-approved protocols, consenting, assessments, blood draws, ECG, medication administration, eSource/data entry, and strong communication skills. Must be bilingual (Spanish) and authorized to work in the US.
Boston or United States or United Kingdom or Canada or London or Oakland or Burlington or Nahant or Arlington or Charlotte or Miami or Portland or Seattle or Toronto or Vancouver or Africa
$49k-$67k/yrOnsiteFull Time
Northeastern University: Private research university located in Boston, Massachusetts.
Bachelor’s degree in psychology, neuroscience, public health, or related field; organizational and communication skills, independent work, and large-scale pediatric or clinical trial data experience required.
Pharmaron CPCShenzhen Stock Exchange / The Stock Exchange of Hong Kong: 300759.SZ / 3759.HK: Public Chinese CRO/CDMO providing integrated drug research, development, and manufacturing services to pharmaceutical, biotech, and medical-device companies.
1+ YOEBachelor of Science in a related field plus 1 year as a Clinical Research Coordinator, or 3 years of clinical research experience.
ClinSpark, Electronic Data Capture (EDC), Microsoft Excel
Nextonic Solutions: Woman-owned federal research solutions partner helping federal health and life-sciences agencies modernize science, data, and technology.
Coordinate recruitment, scheduling, travel and admission of research participants; maintain medical records and EMR entries; communicate with patients, families and clinical staff; create reports and training materials.
Clinical Trials Research Assistant Professor Faculty Position at the Wilmer Eye Institute
Baltimore, Maryland, United States
$100k/yrOnsiteFull Time
Johns Hopkins University School of Medicine: Private nonprofit medical school serving students, scientists, physicians, and patients through education, research, and clinical care.
MD and MPH required; 100% clinical-trials focus; prior clinical research experience in retinal disease and ocular oncology; expertise in trial design, start-up, IRB submissions, adverse event reporting, iMetadata data entry, supervising coordinators, sponsor/CRO communication, and FDA/EMA audits.
The Geneva Foundation: U.S. nonprofit military medical research organization advancing service-member health through research, education, and program support.
2+ YOEBachelor’s degree or equivalent experience, 2–4 years of clinical research experience, IRB submission or compliance monitoring experience, regulatory knowledge, communication skills, organization, and Microsoft Office proficiency.
Microsoft Excel, Microsoft Office, Institutional Review Board (IRB), IACUC