Top 5 Research coordinator Jobs in Frederick Md

Clinical Research Coordinator I
U.S. Dermatology Partners —Rockville, MD
- $55,000 - $65,000 a year
- Full-time
- Vital signs
- Microsoft Outlook
- Computer literacy
- Paid holidays
- Health insurance
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Clinical Research Coordinator II-Rockville/Bethesda
Maryland Oncology —Rockville, MD
- $58,798 - $77,435 a year
- OSHA
- Patient monitoring
- HIPAA
Clinical Research Coordinator
Virginia Heart —Leesburg, VA
- Full-time
- Microsoft Word
- Spanish
- Microsoft Outlook
- Disability insurance
- Health insurance
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Biomedical Research Grants Coordinator
Knowesis, Inc. —Fort Detrick, MD
- $50,000 - $65,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- Organizational skills
- Disability insurance
- Health insurance
Senior Study Coordinator
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $67,900 - $101,000 a year
- Mid-level
- Office
- Master's degree
- Paid parental leave
- AD&D insurance
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Dermatology Medical Assistant
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Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…
10d
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator I

U.S. Dermatology Partners -
Rockville, MD

Quick Apply

Job Details

Full-time
$55,000 - $65,000 a year

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Computer operation
HIPAA compliance
Microsoft Outlook
Computer literacy
Spreadsheets
Writing skills
Basic math
HIPAA
English
ICH guidelines
Desktop applications
Clinical quality assurance standards
Grammar Experience

Full Job Description

Job Summary:

Under the general supervision of a physician and the clinical and clinical research team in an outpatient setting, the Clinical Research Coordinator I (CRC I) is responsible for executing study-related activities from study startup through closeout. All tasks are conducted in compliance with Good Clinical Practice (GCP), ALCOA-C principles, sponsor requirements, and USDP standards. The CRC I supports the Principal Investigator in the conduct of clinical trial visits, ensuring that participants are appropriately scheduled and that all protocol-specified procedures are completed accurately and in a timely manner.

Duties and Responsibilities:

Maintain all aspects of study protocol during recruitment, screening, enrollment, and follow-up visits
Assist the PI, and team when applicable, the informed consent process with patients and their families
Conduct and coordinate patient visits including patient demography, vitals, EKG, phlebotomy, photography, administering investigational drug, assisting PI and sub-investigators with physical exam, and scheduling appropriate follow-up visits
Communicate frequently with contract research organizations, IRB, Sponsors, Central Lab Facilities, and other outside vendors to manage the day-to-day needs for current and prospective trials
Maintain all source documents and investigational drug accountability records

Enter source data into EDC efficient and accurately
Maintain regulatory documents related to ISF
Follow SOPs, policies, and procedures as set forth by the company
Review EDC for accuracy and completion, and resolve queries as they arise
Assists with direct patient care procedures, as required by the study, including biopsies, surgeries, cosmetic procedures and related tasks
Process prescriptions and prior authorizations as directed by physician. Address patient and/or pharmacy questions concerning medication. Enroll patients in patient education/assistance programs
Ensure necessary study related documentation and correspondence study subjects, study teams, vendors, and sponsors
Scans correspondence into EMR
Practices safety, environmental, and/or infection control methods
Assist clinical research manager in delegated tasks
Performs miscellaneous job-related duties as assigned
Process blood and urine samples in accordance with IATA and OSHA standards
Prepare necessary documentation for SIV, IMV, COVs and other sponsor related meetings
Working knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol

Experience Requirements:

At least 1 year of research experience, preferred
At least 1 year of direct patient experience, preferred

Knowledge, Skills and Abilities Requirements:

Meticulously detail oriented, professional attitude, reliable
Organizational skills to support accurate record-keeping
Ability to follow verbal & written instructions
Interpersonal skills to work as a team with patients and outside parties
Able to communicate effectively in English, both verbally and in writing, with proper grammar and spelling skills to avoid mistakes or misinterpretations
Mathematical and analytical ability for basic to intermediate problem solving
Basic to intermediate computer operation
Proficiency with Microsoft Excel, Word, and Outlook
Specialty knowledge of systems relating to job function
Knowledge of state and federal regulations such as ICH GCP, IATA; general understanding of HIPAA guidelines

Supervisory Responsibilities:

This position has no supervisory responsibilities.

Benefits:

Medical, Dental, & Vision
401k
PTO & Paid Holidays
Company Paid Life Insurance
Employee Perks Program

Quick Apply

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research coordinator jobs in frederick md

Clinical Research Coordinator I

Clinical Research Coordinator II-Rockville/Bethesda

Clinical Research Coordinator

Biomedical Research Grants Coordinator

Senior Study Coordinator

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