Top 5 Clinical research assistant Jobs in Dothan, Al

Clinical Research Nurse Coordinator
Digestive Health Specialists —Dothan, AL
- Full-time
- Nursing
- RN License
- Computer literacy
- Health insurance
- Dental insurance
Quick Apply
2d
RN for Clinical Research Coordinator
SEC Clinical Research —Dothan, AL
- $28 - $36 an hour
- Full-time
- Nursing
- Mid-level
- In-person
- Health insurance
- Dental insurance
Quick Apply

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Manages complex administrative tasks in support of research administration and clinical trials, including but not limited to screening patients, entering/…
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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 Nurse Coordinator

Digestive Health Specialists -
Dothan, AL

Quick Apply

Job Details

Full-time
2 days ago

Benefits

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

Qualifications

Computer operation
Nursing
Clinical research
RN License
Employee relationship building
Medication pass administration
Monitoring and managing IVs
Initial patient assessment
Attention to detail
Data entry
Associate's degree
Subcutaneous (SubQ) medication administration
Stakeholder relationship building
Nursing

Full Job Description

Clinical Research Nurse Coordinator

JOB DESCRIPTION

Job Summary

Under the general direction of the Physician Principal Investigator and Site Manager, performs duties associated with coordinating and implementing complex gastroenterology clinical trials. The Clinical Research Nurse Coordinator will work closely with physicians and the clinical team to identify appropriate patients, coordinate study visits, administer study medications, closely monitor research participants, and perform data collection and reporting.

CHARACTERISTIC JOB TASKS AND RESPONSIBILITIES

May include any and/or all of the following:

Coordinates and manages aspects of clinical trials, including communication with sponsors and regulatory authorities.
Identifies and recruits potential study participants, including assessing eligibility, discussing research opportunities, and participating in the informed consent process.
Coordinates and documents research visits and procedures, including obtaining and processing laboratory specimens, obtaining vital signs and ECGs, adverse event and safety monitoring, and administration of study medications, including IV, subcutaneous, and oral medications.
Maintains close communication with the Principal Investigator and/or Sub-Investigator regarding patient status, safety concerns, adverse events, and other clinically significant findings.
Recognizes changes in patient condition and promptly notifies the Principal Investigator and/or Sub-Investigator when physician assessment or intervention is needed.
Documents investigational drug accountability, including drug receipt, storage, preparation, dispensing, and return.
Performs data collection and management, source document collection, electronic data entry, filing and archiving, monitoring visit coordination, and query management.
Assists the Principal Investigator with administrative tasks associated with the day-to-day operations of research studies and projects.
Maintains compliance with applicable research regulations, study protocols, and Good Clinical Practice requirements.

KNOWLEDGE, SKILLS, ABILITIES AND PERSONAL CHARACTERISTICS

Strong clinical judgment
Strong nursing and patient assessment skills
Excellent written and verbal communication skills
Strong interpersonal and relationship-building skills
Strong organizational and analytical skills
Exceptional attention to detail
Ability to maintain confidentiality
Ability to operate a personal computer and various software packages
Proactive and self-directed
Ability to recognize and appropriately escalate changes in patient condition
Conscientious and precise delivery of work, even under pressure

MINIMUM QUALIFICATIONS

Education and experience equivalent to:

Current Registered Nurse (RN) license required.
Strong clinical judgment and patient assessment skills required.
Excellent attention to detail and communication skills required.
Ability to administer IV, subcutaneous, and oral medications within the scope of RN licensure.
Clinical research experience preferred but not required.

Job Type: Full-time

Benefits:

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

Education:

Associate (Preferred)

Experience:

Clinical Research: 1 year (Preferred)

Work Location: In person

Quick Apply

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clinical research assistant jobs in dothan, al

Clinical Research Nurse Coordinator

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