Research Study Coordinator- Clinical Trails Hurwitz

Frederick Health Hospital, Inc.; Frederick (MD); On-site; USD 60,000 - 86,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Life insurance

Paid time off

403B retirement plan

Educational assistance

Employee Assistance Program

Financial planning services

Job summary

Frederick Health Hospital, Inc. is seeking a Research Study Coordinator to support clinical trial activities under the guidance of the Clinical Manager. You will coordinate patient visits, consent and eligibility, and manage regulatory documentation and study data.

The role requires experience in clinical trials, strong organizational and communication skills, and the ability to handle confidential information with sensitivity. Oncology exposure is a plus, and a bachelor’s degree is preferred.

Qualifications

• Detailed knowledge of clinical trials, protocols and policies.
• Excellent written and verbal communication.
• Strong organizational skills and ability to multitask.
• Maintains confidentiality of employee and patient information.

Responsibilities

• Coordinate patient screening, enrollment and visits for clinical trials.
• Maintain regulatory documentation, data and study inventories.
• Submit patient registrations/randomization and ensure data accuracy.
• Collaborate with physicians and multidisciplinary teams to align workflows with study requirements.
• Assist with invoicing and revenue capture as outlined in contracts.
• Represent the Clinical Trials department at IRB and investigator meetings.
• Participate in quality improvement activities within Clinical Trials.

Skills

Clinical trials knowledge

Organizational skills

Communication skills

Confidentiality

Prioritization

Education

Bachelor's degree (preferred)

Job description

Research Study Coordinator- Clinical Trails Hurwitz

Job Category: Allied Health

Requisition Number: RESEA012675

• Posted : September 24, 2026
• Full-Time

Locations

Showing 1 location

1562 Opossumtown Pike
Frederick, MD 21702, USA

Description

Job Summary

Supports, and is responsible for incorporating into job performance, the Frederick Health (FH) mission, vision, core values and customer service philosophy and adheres to the FH Compliance Program, including following all regulatory requirements and the FH Standards of Behavior.

Under the direction of the Clinical Manager, coordinates the research care delivery with the principal investigator, and other members of the clinical research team. Maintains detailed knowledge of all active clinical trials studies and coordinates workflows and processes that provide effective patient management. Assists the clinicians in patient study visits and study procedure. Responsible for the coordination and maintenance of regulatory documentation, electronic study data, site registration status, and product inventory. Works closely with the research clinicians in reviewing potential new studies, initiating new approved studies, and patient screening for potential eligibility. Represents the Clinical Trials department at IRB and investigator meetings. Coordinates invoicing and revenue capture according to study contracts. Actively participates in performance and quality improvement activities within the Clinical Trials department.

Example of Essential Functions:

• Maintains detailed knowledge of clinical trials studies for effective patient coordination.
• Assists research clinicians with patient screening, on-study treatment visits, off-treatment/survival follow-up.
• Coordinates patient consenting process, patient eligibility, and enrollment tracking and documentation.
• Responsible for the electronic submission of patient registration/randomization.
• Maintains inventory of investigation product.
• Performs phlebotomies as needed.
• Reviews lab results for patients on study treatment to determine study treatment dose changes as necessary.
• Coordinates visit specific study lab kits as necessary and manage lab kit inventory and supplies for each study.
• Coordinates study specific blood specimen and tumor specimen processing, storage, and shipment.
• Responsible for timely and accurate data submissions, data queries, follow-up forms, and case report forms.
• Coordinates with Clinical Research Monitors for on-site data audits.
• Processes all IND Safety Alerts on a monthly basis.
• Maintains site registration status.
• Collaborates with physicians and multidisciplinary medical teams to establish workflows and protocols that align with study requirements.
• Supports and participates in performance and quality improvement activities within the Clinical Trials department.
• Responsible for invoicing and revenue capture as outlined in study contracts.
• Participates in community events related to the Frederick Health Clinical Trials Program.

Required Knowledge, Skills and Abilities:

• Detailed knowledge of clinical trials studies, protocols, and policies.
• Strong organizational skills.
• Able to prioritize and manage multiple tasks.
• Excellent written and verbal communication skills.
• Able to assess and care for patients with special needs with respect to cultural, ethical, and religious differences and physical abilities.
• Able to maintain a high level of confidentiality related to employee and patient information.

Minimum Education, Training, and Experience Required:

• A detailed knowledge of research protocols and regulations. At least three years of experience in a Clinical Trials setting required.
• Oncology experience highly desirable.
• A Bachelor’s degree in a healthcare or research related field preferred.
• Excellent written and verbal communication skills. Detail oriented.
• Strong organizational skills and ability to prioritize and manage multiple tasks.
• Able to maintain a high level of confidentiality related to employee and patient information Able to assess and care for patients with special needs with respect to cultural, ethical, and religious differences and physical abilities.
• Maintains continuing education regarding clinical research and patient care with regard to protocol administration.

Must demonstrate and maintain current knowledge and skills in providing appropriate care/contact for patients in the following age groups:

• __ Neonate (0 thru 30 days)
• __ Infant (31 thru 12 months)
• __ Child (13 months thru 12 years)
• X Adolescent (13 years thru 17 years)
• X Adult (18 years thru 65 years)
• X Geriatric (66+ years)

Physical Demands:

Light Work - Lifting up to 20 pounds on an infrequent basis (less than one lift every three minutes and/or carrying up to 10 pounds, or requiring walking or standing to a significant degree (about six [6] hours a day).

Ergonomic Risk Factors:

Repetition : Repeating the same motion over and over again places stress on the muscles and tendons. The severity of risk depends on how often the action is repeated, the speed of the movement, the required force and muscles involved.

Working Conditions:

• Bloodborne Pathogens Exposure Risk: Category A – WILL have exposure to blood or body fluids.

Reporting Relationship:

Reports to the Manager of Oncology

Caring for you as you care for the CommUNITY

Frederick Health offers a comprehensive and affordable benefits package.

• Health, Dental and Vision insurance are offered the 1st of the month after 30 days of employment to all employees hired to work at least 20 hours per week and we offer multiple plans to best meet your and your family's needs.
• Life insurance, Short-Term Income Replacement and Long-Term Disability are employer paid for eligible employees.
• Frederick Health offers a robust Paid Time Off program for eligible employees.
• Our 403B retirement plan helps you save for your retirement and includes an employer match to eligible employees.
• All employees have access to free financial planning sessions.
• We also offer an educational assistance program to support your education goals as well as an employer paid Employee Assistance Program.

Pay is based on experience, skills and education. If position is part-time, salary will be pro-rated based on scheduled hours. The pay range may also vary within the stated range based on specialty if applicable. Non-Exempt positions may have shift differential and/or Overtime paid, if applicab

Salary Range: $60,028.80 - $85737.60

Equal Opportunity Employer
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