UNKNOWN

ADAPTED_NOW

Organize complex components of various clinical trials, including the coordination of study-required testing and procedures, as well as investigational treatment for a variety of conditions and symptoms. Close collaboration with physician investigators required to ensure safe and compliant investigational treatment or intervention and follow-up per the established research protocol.

HOUR

Careers With PurposeSanford Health is one of the largest and fastest-growing not-for-profit health systems in the United StatesWe're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprintFacility: Cancer Center Building Location: Sioux Falls, SD Address: 1309 W 17th St, Sioux Falls, SD 57104, USA Shift: 8 Hours - Day Shifts Job Schedule: Full time Weekly Hours: 40.00 Salary Range: $24.00 - $38.50 Department Details Attire is either business casual or navy blue scrubs; lab coats are also provided by the department Flexibility for things like appointments/kid drop off Ability to WFH 1x per week after 6 months Collaborative team approach and supportive management team Opportunities for continued learning and professional development Emphasis on employee wellbeing through annual events and team building activities Job Summary Provides an opportunity to learn daily and contribute to treatments of the futureEnthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel about the research processOrganize complex components of various clinical trials, including the coordination of study-required testing and procedures, as well as investigational treatment for a variety of conditions and symptomsParticipate in listing and clarifying questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study proceduresSchedule and coordinate pre-study site visitsMonitor enrollment goals and modify recruitment plan as necessaryMaintain patient screening/enrollment logs and appropriately update sponsors, contract research organizations (CROs) and/or senior medical officers (SMOs)Assure the completion of all screening, eligibility and enrollment proceduresConduct interviews to assess subject ability and willingness to follow and complete study procedures and visitsFollow randomization procedures per protocolSchedule subjects for follow-up visitsReview diaries and questionnaires completed by subjectsEnsure appropriate specimen collection, batching and shipping as requiredCollect source documents for sponsor or audit reviewAssess subject compliance with the test article and follow-up visitsAbstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheetsReview inclusion/exclusion criteria to assure subject eligibility, and review with physician investigator for final sign-offReview and verify required source documents in subject medical records to confirm study eligibilityReview study protocol, informed consent form and follow-up procedures with potential study subjectsPrepare case report forms for sponsor or audit reviewResponsible for insurance pre-authorization for study participation, as applicable by studyClose collaboration with physician investigators required to ensure safe and compliant investigational treatment or intervention and follow-up per the established research protocolDocument and maintain all study-related procedures, processes and events by planning and design of new forms/source document tools to use in protocol implementationDocument protocol deviations and exemptionsObtain and review original source documents as neededRecord accurate and timely data onto case report formsMaintain source documentation for all case report entries, as applicableKey in data for electronic submission, if applicableCorrect and edit case report form entries as appropriateResolve data queriesEnsure drug/device accountability by completing appropriate documentations per individual protocolsSchedule and participate in sponsor monitoring visits and audits to ensure compliance with regulatory requirements governing clinical researchMeet with monitors/auditors during routine visits to discuss case report form completion, query resolution and other protocol-related issuesTravel between the Sioux Falls, SD site and the Worthington, MN site may be requiredQualifications Bachelor's degree in biology, microbiology or related fieldMay consider graduates of an accredited school of practical nursing as a Licensed Practical Nurse (LPN) dependent on facility and department needsMinimum three years of clinical or clinical research experience or six to eight years of relevant work experience requiredIf a Licensed Practical Nurse (LPN), currently holds an unencumbered LPN license with state nursing board and/or possess multi-state licensure privilegesObtains and subsequently maintains required department specific competencies and certificationsBenefits Sanford Health offers an attractive benefits package for qualifying full-time and part-time employeesDepending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balanceFor more information about Total Rewards, visit https://sanfordcareers.com/benefits Sanford is an EEO/AA Employer M/F/Disability/VetIf you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org Sanford Health has a Drug Free Workplace PolicyAn accepted offer will require a drug screen and pre-employment background screening as a condition of employmentReq Number: R-0244700 Job Function: Research Featured: No

Sanford Health

Clinical Research Coordinator

Biology

Cancer

Case Report Form (CRF)

Clinical Research

Clinical Trial

Contract Research Organization (CRO)

Event Management

Informed Consent

Insurance

Interviewing Skills

Medical Records

Microbiology

Nonprofit

Organizational Skills

Reporting Skills

Research Protocols

Team Player

Testing

Vendor/Supplier Selection

Kellogg Company

Graduate from a nationally accredited nursing program preferred, including, but not limited to, Commission on Collegiate Nursing Education (CCNE), Accreditation Commission for Education in Nursing (ACEN), and National League for Nursing Commission for Nursing Education Accreditation (NLN CNEA). Clinical skills that may be required include, but not limited to: patient assessment for adverse events and assistance with, or completion of, study related procedures as detailed in the research protocol (ex: injections, phlebotomy, or infusions), within the applicable state scope of practice.

**Careers With Purpose** **Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America’s heartland.** **Facility:** Cancer Center Building **Location:** Sioux Falls, SD **Address:** 1309 W 17th St, Sioux Falls, SD 57104, USA **Shift:** 8 Hours - Day Shifts **Job Schedule:** Full time **Weekly Hours:** 40.00 **Salary Range:** $27.50 - $44.00 **Department Details** Based on site in Sioux Falls, SD, this role offers the opportunity to build valuable experience in clinical research while working across a variety of studies. You will engage directly with patients, physicians, nurses, and research teams to support each step of the research process. As a RN Clinical Research Coordinator, you will manage key components of study operations, including outreach, patient recruitment, conducting interviews, answering participant questions, scheduling, and coordinating tests and procedures. Success in this role requires strong communication skills, a collaborative mindset, and a genuine passion for providing excellent patient care. What's In It For You? * Dynamic, supportive team * Ability to WFH 1x per week after 6 months * Monday - Friday flexible schedule Emphasis on employee wellbeing and team building events **Job Summary** Provides an opportunity to learn daily and contribute to treatments of the future. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel to the research process. Advanced nursing position that involves clinical patient contact, research study coordination and study data management. Must be able to organize complex components of clinical trials, including test ordering, procedure scheduling and insurance pre-authorization for participants, if applicable. Clinical skills that may be required include, but not limited to: patient assessment for adverse events and assistance with, or completion of, study related procedures as detailed in the research protocol (ex: injections, phlebotomy, or infusions), within the applicable state scope of practice. Demonstrate a desire and ability to strictly adhere to all levels of institutional, state and federal regulations and established research protocols, and the ability to collaborate with physician investigators to ensure safe and compliant investigational treatment or intervention and follow-up. Attend investigator meetings and coordinate pre-study site visits. Monitor enrollment goals and modify recruitment plan as needed. Ensure the completion of all screening, eligibility and enrollment procedures. Work with pharmacy to dispense study articles and provide subject education. Clarify questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures. Review inclusion/exclusion criteria to assure subject eligibility and review with physician investigator. Review study protocol, informed consent form and follow-up procedures with potential study subjects. Schedule subjects for follow-up visits to review diaries and questionnaires. Ensure appropriate specimen collection, batching and shipping as required. Document and maintain all study-related procedures, processes and events. Document protocol deviations and exemptions and record accurate and timely data. Maintain accurate source documentation for all case report entries and input data for submission. Required to use appropriate nursing assessment skills to evaluate patient condition in response to study intervention. Collect data regarding patient condition for review by the physician investigator. Prepare case report forms and source documents for sponsor review. Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets. Communicate effectively with subjects, research team, Institutional Review Board (IRB) and sponsor representatives. Occasional local travel between sites and student supervision may be required. **Qualifications** Graduate from a nationally accredited nursing program preferred, including, but not limited to, Commission on Collegiate Nursing Education (CCNE), Accreditation Commission for Education in Nursing (ACEN), and National League for Nursing Commission for Nursing Education Accreditation (NLN CNEA). Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in a Nurse Licensure Compact (NLC) state. Obtains and subsequently maintains required department specific competencies and certifications. **Benefits** Sanford offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit https://sanfordcareers.com/benefits . Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org . Sanford has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment. **Req Number:** R-0259725 **Job Function:** Research **Featured:** No

Registered Nurse - Clinical Research Coordinator

Adverse Events

Clinical Nursing

Communication Skills

Data Collection

Data Management

Federal Laws and Regulations

Healthcare

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Injections

Nursing

Nursing Credentials

Patient Assessment

Patient Care

Pharmacy

Phlebotomy

Registered Nurse (RN)

Research Nursing

State Laws and Regulations

Training/Teaching

Sanford Health Jobs

Embedded within Sanford Health, one of the nation’s largest nonprofit integrated health systems, Sanford Research offers a unique opportunity to help translate research into clinical impact—accelerating the path from bench to bedside and into the communities we serve. Sanford Research is seeking a Manager of Research Operations to play a pivotal role in supporting and helping researchers advancing basic, translational, and clinical research across our organization.

**Careers With Purpose** **Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America’s heartland.** **Facility:** Sanford Center Building **Location:** Sioux Falls, SD **Address:** 2301 East 60th St N, Sioux Falls, SD 57104, USA **Shift:** 8 Hours - Day Shifts **Job Schedule:** Full time **Weekly Hours:** 40.00 **Department Details** Sanford Research is seeking a Manager of Research Operations to play a pivotal role in supporting and helping researchers advancing basic, translational, and clinical research across our organization. This leader is responsible for maintaining and strengthening the administrative and logistical infrastructure that enables investigators and scientific staff to focus on discovery, innovation, and improving patient outcomes. Embedded within Sanford Health, one of the nation’s largest nonprofit integrated health systems, Sanford Research offers a unique opportunity to help translate research into clinical impact—accelerating the path from bench to bedside and into the communities we serve. Why This Role Matters You will be a central enabler of scientific discovery, ensuring the systems, workflows, and resources supporting research are efficient, scalable, and compliant. Your work directly supports research with real-world clinical and community impact, aligning science with Sanford Health’s mission to improve health outcomes. You will collaborate closely with research leaders to shape resource allocation, operational strategy, and long-term research success. At Sanford Research, you won’t just support research—you’ll help enable discoveries that improve lives. If you are passionate about research operations, leadership, and making a meaningful impact through science and healthcare, we invite you to apply. **Job Summary** The Manager of Research Operations is responsible for maintenance of administrative and logistical support infrastructure of basic, translational and clinical research labs and studies. Responsibilities may include development and maintenance of centralized programs, workflows and processes required for success of investigators and scientific staff and supervision of support staff. May be assigned roles within regulatory programs and work as liaison with corporate service departments. Assist research leadership with budgeting and resource allocation and strategic planning efforts. **Qualifications** Bachelor's degree required in a science or related field and five years of scientific and or administrative experience or a Master's degree with three years of scientific and/or administrative experience. Current valid Category II driver’s license, and meet all medical guidelines for Sanford Health Category II drivers. **Benefits** Sanford offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit https://sanfordcareers.com/benefits . Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org . Sanford has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment. **Req Number:** R-0259534 **Job Function:** Research **Featured:** No

Manager, Research Operations

Online Research Jobs in Sioux Falls, SD

Online Research Jobs in Sioux Falls, SD

Resume Resources

Get noticed by top employers!

Online Research Jobs in Sioux Falls, SD

Clinical Research Coordinator Sanford Health

Registered Nurse - Clinical Research Coordinator Sanford Health

Manager, Research Operations Sanford Health

Resume Resources