Clinical Research Coordinator I Oncology

AdventHealth; Altamonte Springs (FL); On-site; USD 50,000 - 70,000; Full time

Job summary

AdventHealth is seeking a Clinical Research Coordinator I to oversee patient recruitment and participation in clinical studies. The role involves coordinating research processes, ensuring regulatory compliance, and providing high-quality service to participants in the Altamonte Springs community. The ideal candidate will have relevant educational credentials and skills in research coordination and patient interaction.

Benefits

Benefits from Day One

Paid Days Off from Day One

Student Loan Repayment Program

Career Development

Qualifications

• Bachelor’s degree in Healthcare or related field or a Bachelor’s degree in any field with research experience.
• Bilingual (English/Spanish) preferred.
• Certified Clinical Research Coordinator (CCRC) preferred.

Responsibilities

• Coordinate patient screening and follow-up for clinical trials.
• Execute and coordinate the informed consent process.
• Collaborate with various departments to ensure regulatory compliance.

Skills

Patient recruitment

Data collection

HIPAA compliance

Collaboration

Concierge level service

Education

Bachelor’s degree in Healthcare or related field

Associate's degree in Healthcare or related field and two years of clinical research experience

Graduate of an accredited allied health certificate program

Job description

All the benefits and perks you need for you and your family:

• Benefits from Day One

• Paid Days Off from Day One

• Student Loan Repayment Program

• Career Development

• Whole Person Wellbeing Resources

• Mental Health Resources and Support

Our promise to you:

Joining AdventHealth is about being part of something bigger. It’s about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that together we are even better.

Schedule: Full Time

Shift : Days

Location: 601 East Altamonte Dr, Altamonte Springs, FL 32701

The community you’ll be caring for: AdventHealth Altamonte Springs

• Located north of Orlando in the community of Altamonte Springs, our facility is consistently named “Best Hospital” for overall quality, reputation, doctors and nurses by local residents

• As the largest satellite campus within the AdventHealth system, AdventHealth Altamonte has been providing state-of-the-art healthcare to the community since 1973

• The 398-bed hospital cares for more than 168,000 patients a year. We are proud to be revolutionizing health care with visionary leadership and world-class resources

The role you’ll contribute:

The Clinical Research Coordinator I (CRC I) is involved in all aspects of research conducted including patient screening, assessing eligibility, and coordinating the care and follow-up of volunteers placed on research studies, trials, and programs. Specific activities to include: Research participant recruitment and consenting for the therapeutic areas they serve, provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies, and the coordination of biospecimen collection (i.e. blood, tissue) through collaborative interaction with Clinical Research nursing staff, laboratory teams, hospital departments to ensure ongoing regulatory and protocol compliance.

The value you’ll bring to the team:

• Execute and coordinate the informed consent process for AdventHealth Research Institute participants in clinical trials and research studies across multiple locations. This may require travel between sites and research laboratories, and/or the use of technology.

• Responsible for all aspects of research conducted including patient screening, assessing eligibility, and coordinating the participation and follow-up of volunteers placed on research studies, trials, and programs.

• Coordinate research participant recruitment and consenting for the therapeutic areas they serve

• Provision of concierge level service for all patient facing interactions during the course of clinical trials and research studies

• Coordinate or perform biospecimen collection (i.e. blood, tissue) and maintain HIPAA protected database connecting patient information to biospecimens used in research; perform patient chart review and data collection.

• Collaborative interaction with Clinical Research nursing staff, Research Services, laboratory teams, hospital departments, and physician offices, to ensure ongoing regulatory and protocol compliance.

• Through collaboration with assistant clinical coordinators, ensures compliant data entry/data mining into registries, patient records, and research specific database systems.

• Assists Principal Investigators and research staff in the development of compliant research protocols and other control documents.

• Serves as the study-specific point of contact for participants, investigators, research staff, hospital departments and external research partners.

• Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the Institutes research division intended to meet standards. Ensures all patient-facing activities are compliant with clinical research standards and AHRI procedures.

• Maintain sensitivity to cost containment measures by conserving hospital supplies, equipment, and human resources while overseeing proposed project budgets from internal and external funding sources.

The expertise and experiences you’ll need to succeed:

Minimum qualifications :

• Bachelor’s degree in Healthcare or related field with no research experience OR Bachelor’s degree in any field with research experience.

• Associates degree in Healthcare or related field and two (2) years of clinical research or healthcare experience or

• Graduate of an accredited allied health certificate program with four (4) years of clinical research or healthcare experience.

Preferred qualifications:

• Bilingual (English/Spanish)

• Master’s degree in Healthcare, Research, or related field

• Certified Clinical Research Coordinator (CCRC) (per the Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SOCRA))

• American Heart Association Basic Life Support (BLS)

• Other certification as applicable to clinical degree or program (i.e. medical assistant, medical technician, phlebotomy)

2/28/22

This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances. The salary range reflects the anticipated base pay range for this position. Individual compensation is determined based on skills, experience and other relevant factors within this pay range. The minimums and maximums for each position may vary based on geographical location.

Category: Research

Organization: AdventHealth Orlando

Schedule: Full-time

Shift: 1 - Day

Req ID: 25017811

We are an equal opportunity employer and do not tolerate discrimination based on race, color, creed, religion, national origin, sex, marital status, age or disability/handicap with respect to recruitment, selection, placement, promotion, wages, benefits and other terms and conditions of employment.