Clinical Research Coordinator

Sioux Center Health; Sioux Falls (SD); On-site; USD 33,000 - 63,000; Full time

Job summary

Avera Cancer Institute-Sioux Falls is seeking a Clinical Research Coordinator/RN - Research Coordinator in Oncology to coordinate assigned clinical studies and oversee regulatory tasks with compassion and professionalism. You will work with patients and families from evaluation through treatment phases to ensure protocol adherence and high-quality patient care.

The role involves coordinating complex oncology trials, complying with FDA regulations, and collaborating across multidisciplinary teams

Qualifications

• Bachelor's degree in a health/science field or equivalent.
• 1–3 years of clinical research, oncology, or hematology experience preferred.
• Knowledge of good clinical practice and FDA regulations.

Responsibilities

• Coordinate multiple complex protocols across cancer research trials.
• Ensure accurate communication of patient status and research interventions.
• Collaborate with investigators, departments, sponsors, and monitors to maintain protocol compliance.

Skills

Clinical research coordination

Regulatory knowledge

Communication skills

Team collaboration

Education

Bachelor's in health sciences

Job description

Pay Range

The pay range for this position is listed below. Actual pay rate dependent upon experience.

Location:

Avera Cancer Institute-Sioux Falls

Worker Type

Regular

Work Shift

Day Shift (United States of America)

Pay Range

The pay range for this position is listed below. Actual pay rate dependent upon experience.

$24.00 - $46.25

Position Highlights

Posting should include information about both the Clinical Research Coordinator position AND RN - Research Coordinator position for Oncology. Only 1 person will be hired for this opening.

You Belong at Avera

Be part of a multidisciplinary team built with compassion and the goal of Moving Health Forward for you and our patients. Work where you matter.

A Brief Overview

Responsible for coordinating assigned clinical research studies by performing diverse clinical, regulatory, and clerical responsibilities requiring analysis, judgment, and knowledge of clinical research. Facilitates clinical research studies with participants, staff, investigators, and sponsoring organizations. The Coordinator works with patients and their families, beginning with evaluation and continuing through all required treatment phases of the clinical trial, in a compassionate and professional manner in order to achieve excellence in quality patient care and fulfill protocol requirements.

What You Will Do

• Coordinates multiple complex protocols at a time, for all drug development phases of the cancer research treatment in working with providers, patients and their family, as well as ancillary departments as needed for patient care coordination.
• Assures all appropriate information in patient cancer treatment status is communicated accordingly, and the research intervention is implemented.
• Collaborates with investigators, ancillary departments, study sponsors, internal and external monitors and auditors to facilitate compliance with the requirements of the research protocol with regards to good clinical research practice, FDA regulations, and policies that affect research at the institutional, state, federal and international level, while remaining cognizant of the needs of diverse patient populations.
• Utilizes multiple communication and research-specific education methods with research, clinical, and organizational staff, as well as patients and their significant others, to facilitate the effective conduct of clinical trials including the promotion and integrity of the clinical trial, and advocates for the safety and care of clinical trial patients.
• Develops and maintains respectful and trustworthy relationships with providers and their clinical staff, ancillary departments, and study sponsors to facilitate compliance with and successful accrual of eligible patients to clinical trials, all while ensuring proper use of and accountability for experimental drugs.
• Demonstrates leadership in ensuring adherence to ethical practices during the conduct of clinical trials to protect the rights and well-being of patients from the time the patients sign the informed consent through their participation duration, including the collection of quality data.
• Uses a variety of resources and strategies to manage the care of patients participating in clinical trials, ensuring education of and compliance with protocol procedures, assessments, treatment, and reporting requirements as well as management of symptoms.
• Assists in implementation of recruitment plans to identify and assess individuals who may be eligible for clinical trials and utilizes a variety of strategies to enhance recruitment while being mindful of the study entry criteria, required procedures, the needs of diverse patient populations, and other potential factors.
• Identifies the financial variables that affect research and supports good financial stewardship in clinical trials, in collaboration with the clinical trial analysts and patient advocates.

Essential Qualifications

The individual must be able to work the hours specified. To perform this job successfully, an individual must be able to perform each essential job function satisfactorily including having visual acuity adequate to perform position duties and the ability to communicate effectively with others, hear, understand and distinguish speech and other sounds. These requirements and those listed above are representative of the knowledge, skills, and abilities required to perform the essential job functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions, as long as the accommodations do not cause undue hardship to the employer.

Required Education, License/Certification, Or Work Experience

• Bachelor's Health and science field
• 1-3 years clinical research, laboratory, or oncology or hematology

Expectations and Standards

• Commitment to the daily application of Avera’s mission, vision, core values, and social principles to serve patients, their families, and our community.
• Promote Avera’s values of compassion, hospitality, and stewardship.
• Uphold Avera’s standards of Communication, Attitude, Responsiveness, and Engagement (CARE) with enthusiasm and sincerity.
• Maintain confidentiality.
• Work effectively in a team environment, coordinating work flow with other team members and ensuring a productive and efficient environment.
• Comply with safety principles, laws, regulations, and standards associated with, but not limited to, CMS, The Joint Commission, DHHS, and OSHA if applicable.

Benefits You Need & Then Some

Avera is proud to offer a wide range of benefits to qualifying part-time and full-time employees. We support you with opportunities to help live balanced, healthy lives. Benefits are designed to meet needs of today and into the future.

• PTO available day 1 for eligible hires.
• Up to 5% employer matching contribution for retirement
• Career development guided by hands-on training and mentorship

Avera is an Equal Opportunity Employer - Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, Veteran Status, or other categories protected by law. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-605-504-4444 or send an email to [e-mail].