Top 11 Clinical research coordinator Jobs in Axis, Al

Clinical Research Coordinator
Southern Cancer Center —Mobile, AL
- Mid-level
- Clinic
- 1 year
14d
Clinical Research Coordinator II
Velocity Clinical Research, Inc. —Mobile, AL
- Full-time
- English
- Mid-level
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
Clinical Research Coordinator
Infirmary Health —Mobile, AL
- Full-time
- Nursing
- Word processing
- Computer literacy
Clinical Affiliations Coordinator
University of South Alabama —Mobile, AL
- Overtime
- Research
- Mid-level
- Administrative experience
Clinical Applications Coordinator - Learning Management Systems - SSO Staff Development
USA Health —Mobile, AL
- Overtime
- Mid-level
- Bachelor's degree
- Computer skills
Clinical Coordinator - Charge Registered Nurse - Dialysis
Fresenius Medical Care —Semmes, AL
- Full-time
- CPR Certification
- Nursing
- RN License

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Clinical Research Coordinator II
Velocity Clinical Research, Inc. —Mobile, AL
Collaborate with Clinical Research Team to develop Quality Control strategy for reviewingone’s work on an ongoing basis and in preparation for monitor visits.
Quick Apply

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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,…
Clinical Research Assistant 2-Hematology
The Ohio State University —Columbus, OH
Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required.
4d

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Clinical Research Coordinator

Southern Cancer Center -
Mobile, AL

Apply Now

Job Details

14 days ago

Qualifications

Desktop applications
Productivity software
Associate's degree

Full Job Description

Overview:

Southern Cancer Center – Springhill Location

Join Our Team!

Southern Cancer Center is seeking a highly organized, detail-oriented, and compassionate Clinical Research Coordinator to join our growing team. This role is critical to advancing cancer care through clinical research by coordinating patient participation in clinical trials and ensuring compliance with study protocols, regulatory requirements, and quality standards.

If you are passionate about improving patient outcomes, enjoy working collaboratively with physicians and research teams, and thrive in a fast-paced healthcare environment, we encourage you to apply.

Position Summary

The Clinical Research Coordinator is responsible for coordinating and managing clinical trial activities, including patient screening, enrollment, data collection, regulatory compliance, and ongoing patient monitoring. This individual works closely with physicians, research sponsors, patients, and other healthcare professionals to ensure successful execution of clinical research studies.

Responsibilities:

Essential Duties & Responsibilities

Patient Recruitment & Clinical Trial Coordination

Screen potential patients for protocol eligibility.
Present clinical trial opportunities and study details to patients and families.
Participate in the informed consent process and enroll eligible patients into clinical trials.
Assist with patient care activities required by study protocols.
Monitor patient participation and ensure protocol compliance throughout the study.

Clinical Research Activities

Collect, enter, and report study data accurately and timely.
In collaboration with physicians, review patients for:
- Changes in condition
- Adverse events
- Concomitant medication use
- Protocol compliance
- Response to study treatment
Thoroughly document all research-related activities and findings.
Maintain accurate and complete study records.

Investigational Drug Management

May dispense investigational medications in accordance with protocol requirements.
Maintain investigational drug accountability and documentation.

Regulatory & Compliance Responsibilities

Assist in the collection, preparation, and maintenance of regulatory documents.
Ensure compliance with US Oncology Research (USOR) Standard Operating Procedures (SOPs), FDA regulations, and Good Clinical Practice (GCP) guidelines.
Participate in monitoring visits, audits, and quality assurance activities.
Schedule and coordinate sponsor monitoring and auditing visits as needed.
Serve as a liaison with study sponsors, monitors, and auditors.

Laboratory & Specimen Management

Assist with collection, preparation, packaging, and shipment of laboratory specimens to central laboratories and vendors.
Complete Hazmat and/or IATA training as required.

Professional Development

Participate in mandatory training, continuing education, and research-related learning opportunities.
Stay current on clinical research regulations, protocols, and best practices.

Qualifications:

Qualifications

Education

Associate degree in a clinical, scientific, or healthcare-related field required.
Bachelor's degree preferred.

Experience

Minimum of one (1) year of experience in a clinical or scientific healthcare setting required.
Oncology experience strongly preferred.
Experience working directly with physicians preferred.
Proficiency in Microsoft Office applications required.

Knowledge, Skills & Abilities

Excellent verbal and written communication skills.
Strong organizational and prioritization skills.
Ability to manage multiple tasks and deadlines simultaneously.
Exceptional time management skills.
Strong interpersonal skills with the ability to work effectively across all levels of the organization.
High degree of accuracy and attention to detail.
Ability to work independently and collaboratively in a fast-paced environment.
Ability to maintain patient confidentiality and professionalism.
May be responsible for performing basic clinical assessments.

Why Join Southern Cancer Center?

At Southern Cancer Center, our mission is to provide compassionate, high-quality cancer care while advancing treatment options through innovative clinical research. As a member of our team, you will have the opportunity to make a meaningful impact on patients' lives while contributing to the future of oncology care.

Working Conditions

Work Environment

Traditional clinical and office environment.
Frequent exposure to conditions common in an oncology/hematology practice, including communicable diseases, toxic substances, ionizing radiation, and medical preparations.
Reasonable accommodations may be made to enable qualified individuals with disabilities to perform essential job functions.

Physical Requirements

Significant computer-based work.
Frequent standing and walking throughout the clinic.
Occasional lifting and carrying of items up to 40 pounds.
Requires corrected vision and hearing within normal ranges.

Apply Today

Become part of a team dedicated to advancing cancer treatment and improving the lives of our patients through exceptional care and innovative research.

Southern Cancer Center is an Equal Opportunity Employer.

Apply Now

Refine Your Search

clinical research coordinator jobs in axis, al

Clinical Research Coordinator

Clinical Research Coordinator II

Clinical Research Coordinator

Clinical Affiliations Coordinator

Clinical Applications Coordinator - Learning Management Systems - SSO Staff Development

Clinical Coordinator - Charge Registered Nurse - Dialysis

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I want to receive the latest job alert for clinical research coordinator in axis, al

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Join Our Team!

Position Summary

Essential Duties & Responsibilities

Patient Recruitment & Clinical Trial Coordination

Clinical Research Activities

Investigational Drug Management

Regulatory & Compliance Responsibilities

Laboratory & Specimen Management

Professional Development

Qualifications

Education

Experience

Knowledge, Skills & Abilities

Why Join Southern Cancer Center?

Working Conditions

Work Environment

Physical Requirements

Apply Today

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