Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now!
Sanford Health
Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now!
Job Description
Clinical Research Coordinator at Sanford Health - Sioux Falls, SD
Role Overview
As a Clinical Research Coordinator at Sanford Health in Sioux Falls, South Dakota, you will play a crucial role in advancing medical knowledge and improving patient outcomes through the management and coordination of clinical trials. This position offers a unique opportunity to contribute to cutting-edge research while working within a collaborative and supportive environment. You will be responsible for organizing complex components of various clinical trials, ensuring adherence to protocols, and maintaining accurate data. Your efforts will directly impact the development of new treatments and therapies.
A Day in the Life
Your day-to-day activities will be diverse and engaging. You will begin by reviewing study protocols and ensuring all necessary materials are prepared. A significant portion of your time will be spent coordinating with investigators, sponsors, and other team members to address any questions or concerns. You will also be responsible for recruiting and screening potential study participants, conducting informed consent procedures, and scheduling follow-up visits.
Data management is another critical aspect of your role. You will abstract data from medical records, complete case report forms, and maintain accurate source documentation. Additionally, you will ensure proper specimen collection and shipping, monitor patient compliance, and document any protocol deviations. Throughout the day, you will collaborate closely with physician investigators to ensure the safety and well-being of study participants.
You'll also enjoy a collaborative team approach, WFH options, and supportive management team.
Why Sioux Falls, South Dakota?
Sioux Falls offers a high quality of life with a low cost of living. The city boasts a thriving job market, excellent schools, and a friendly community. Residents enjoy a variety of recreational activities, including hiking, biking, and water sports. The city also has a vibrant arts and culture scene, with numerous museums, theaters, and music venues. Sioux Falls is a great place to raise a family or start a career.
Career Path
Sanford Health is committed to providing opportunities for career growth and advancement. As a Clinical Research Coordinator, you can progress to roles such as Senior Clinical Research Coordinator, Clinical Research Manager, or even pursue a career in clinical research administration. Sanford Health also offers opportunities for professional development and continuing education to help you enhance your skills and knowledge.
Salary & Benefits
The estimated salary range for a Clinical Research Coordinator in Sioux Falls, South Dakota is $45,000 to $75,000 per year. Sanford Health offers a comprehensive benefits package, including health insurance, paid time off, retirement plan, and tuition reimbursement. Additionally, employees have access to wellness programs, employee discounts, and other perks.
Sanford Health Culture
Sanford Health is dedicated to the work of health and healing. Our organization is proud to offer 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 footprint. You’ll enjoy opportunities for continued learning and professional development, and an emphasis on employee wellbeing through annual events and team building activities. We value teamwork, respect, and innovation, and we strive to create a positive and supportive work environment for all employees.
How to Apply
To apply for the Clinical Research Coordinator position at Sanford Health, please visit our careers page and submit your application online. Be sure to highlight your relevant skills and experience, and explain why you are interested in this opportunity.
FAQ
- What qualifications are required for this position? A bachelor's degree in a related field and previous experience in clinical research are preferred.
- What are the key responsibilities of a Clinical Research Coordinator? Key responsibilities include coordinating clinical trials, managing data, and ensuring protocol adherence.
- What is the salary range for this position? The estimated salary range is $45,000 to $75,000 per year.
- What benefits does Sanford Health offer? Sanford Health offers a comprehensive benefits package, including health insurance, paid time off, and retirement plan.
- What is the work environment like at Sanford Health? The work environment is collaborative, supportive, and focused on teamwork and innovation.
- What opportunities for career advancement are available? Opportunities for advancement include roles such as Senior Clinical Research Coordinator and Clinical Research Manager.
- Is prior experience in clinical research required? While prior experience is preferred, it is not always required. Strong organizational and communication skills are also highly valued.
- What type of training is provided for this role? Sanford Health provides training on clinical trial protocols, data management systems, and regulatory guidelines.
- What is the typical work schedule for this position? The typical work schedule is 8 Hours - Day Shifts (United States of America).
- What kind of professional development opportunities are there? There are opportunities for continued learning and professional development.
Locations
- Sioux Falls, South Dakota, United States
Salary
49,500 - 82,500 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical Trial Coordinationintermediate
- Data Managementintermediate
- Patient Recruitmentintermediate
- Regulatory Complianceintermediate
- Informed Consentintermediate
- Source Documentationintermediate
- Case Report Form (CRF) Completionintermediate
- Data Abstractionintermediate
- Specimen Collection and Shippingintermediate
- Protocol Adherenceintermediate
- Deviation Reportingintermediate
- Electronic Data Capture (EDC)intermediate
- Communication Skillsintermediate
- Organizational Skillsintermediate
- Time Managementintermediate
- Problem-Solvingintermediate
- Attention to Detailintermediate
- Medical Terminologyintermediate
- HIPAA Complianceintermediate
- GCP (Good Clinical Practice)intermediate
- ICF (Informed Consent Form)intermediate
- Sponsor Communicationintermediate
- CRO (Contract Research Organization) Communicationintermediate
- Investigator Collaborationintermediate
Required Qualifications
- Bachelor's degree in a related field (e.g., Biology, Nursing, Public Health) (experience)
- Previous experience in clinical research preferred (experience)
- Knowledge of clinical trial regulations and guidelines (e.g., FDA, GCP) (experience)
- Strong understanding of medical terminology (experience)
- Proficiency in data management and analysis (experience)
- Excellent communication and interpersonal skills (experience)
- Ability to work independently and as part of a team (experience)
- Detail-oriented and organized (experience)
- Ability to prioritize and manage multiple tasks (experience)
- Experience with electronic data capture (EDC) systems (experience)
- Familiarity with informed consent procedures (experience)
- Knowledge of HIPAA regulations (experience)
- Ability to maintain patient confidentiality (experience)
- Experience with regulatory submissions (e.g., IRB) (experience)
- Certification in clinical research (e.g., SoCRA, ACRP) preferred (experience)
Responsibilities
- Organize and coordinate various clinical trials.
- Coordinate study-required testing and procedures.
- Coordinate investigational treatment for a variety of conditions and symptoms.
- Participate in clarifying questions and concerns with investigators and sponsors.
- Schedule and coordinate pre-study site visits.
- Monitor enrollment goals and modify recruitment plans as necessary.
- Maintain patient screening/enrollment logs and update sponsors, CROs, and SMOs.
- Ensure completion of all screening, eligibility, and enrollment procedures.
- Conduct interviews to assess subject ability and willingness to follow study procedures.
- Follow randomization procedures per protocol.
- Schedule subjects for follow-up visits.
- Review diaries and questionnaires completed by subjects.
- Ensure appropriate specimen collection, batching, and shipping.
- Collect source documents for sponsor or audit review.
- Assess subject compliance with the test article and follow-up visits.
- Abstract data from medical records and consultation notes.
- Prepare study forms and flow sheets.
- Review inclusion/exclusion criteria to assure subject eligibility.
- Review study protocol, informed consent form, and follow-up procedures with potential subjects.
- Prepare case report forms for sponsor or audit review.
- Manage insurance pre-authorization for study participation.
- Collaborate with physician investigators to ensure safe and compliant treatment.
- Document and maintain all study-related procedures, processes, and events.
- Document protocol deviations and exemptions.
- Record accurate and timely data onto case report forms.
- Maintain source documentation for all case report entries.
- Key in data for electronic submission.
- Correct and edit case report form entries as appropriate.
- Resolve data queries.
- Ensure drug/device accountability by completing appropriate documentation.
Benefits
- general: Comprehensive health insurance (medical, dental, vision)
- general: Paid time off (PTO) and holidays
- general: Retirement plan with employer matching
- general: Life insurance and disability coverage
- general: Flexible spending accounts (FSA) or health savings accounts (HSA)
- general: Employee assistance program (EAP)
- general: Tuition reimbursement or assistance
- general: Professional development opportunities
- general: Employee discounts
- general: Wellness programs
- general: On-site fitness center or gym membership discounts
- general: Childcare assistance or resources
- general: Relocation assistance (if applicable)
- general: Career advancement opportunities within Sanford Health
- general: Supportive and collaborative work environment
- general: Opportunity to contribute to medical advancements
- general: Work-life balance initiatives
- general: Employee recognition programs
- general: Short-term disability
- general: Long-term disability
- general: Voluntary benefits (e.g., supplemental life insurance, accident insurance)
- general: Legal assistance
- general: WFH options (after 6 months)
- general: Lab Coats Provided
- general: Team Building Activities
Tags & Categories
Answer 10 quick questions to check your fit for Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now! @ Sanford Health.
Related Books and Jobs
Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now!
Sanford Health
Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now!
Job Description
Clinical Research Coordinator at Sanford Health - Sioux Falls, SD
Role Overview
As a Clinical Research Coordinator at Sanford Health in Sioux Falls, South Dakota, you will play a crucial role in advancing medical knowledge and improving patient outcomes through the management and coordination of clinical trials. This position offers a unique opportunity to contribute to cutting-edge research while working within a collaborative and supportive environment. You will be responsible for organizing complex components of various clinical trials, ensuring adherence to protocols, and maintaining accurate data. Your efforts will directly impact the development of new treatments and therapies.
A Day in the Life
Your day-to-day activities will be diverse and engaging. You will begin by reviewing study protocols and ensuring all necessary materials are prepared. A significant portion of your time will be spent coordinating with investigators, sponsors, and other team members to address any questions or concerns. You will also be responsible for recruiting and screening potential study participants, conducting informed consent procedures, and scheduling follow-up visits.
Data management is another critical aspect of your role. You will abstract data from medical records, complete case report forms, and maintain accurate source documentation. Additionally, you will ensure proper specimen collection and shipping, monitor patient compliance, and document any protocol deviations. Throughout the day, you will collaborate closely with physician investigators to ensure the safety and well-being of study participants.
You'll also enjoy a collaborative team approach, WFH options, and supportive management team.
Why Sioux Falls, South Dakota?
Sioux Falls offers a high quality of life with a low cost of living. The city boasts a thriving job market, excellent schools, and a friendly community. Residents enjoy a variety of recreational activities, including hiking, biking, and water sports. The city also has a vibrant arts and culture scene, with numerous museums, theaters, and music venues. Sioux Falls is a great place to raise a family or start a career.
Career Path
Sanford Health is committed to providing opportunities for career growth and advancement. As a Clinical Research Coordinator, you can progress to roles such as Senior Clinical Research Coordinator, Clinical Research Manager, or even pursue a career in clinical research administration. Sanford Health also offers opportunities for professional development and continuing education to help you enhance your skills and knowledge.
Salary & Benefits
The estimated salary range for a Clinical Research Coordinator in Sioux Falls, South Dakota is $45,000 to $75,000 per year. Sanford Health offers a comprehensive benefits package, including health insurance, paid time off, retirement plan, and tuition reimbursement. Additionally, employees have access to wellness programs, employee discounts, and other perks.
Sanford Health Culture
Sanford Health is dedicated to the work of health and healing. Our organization is proud to offer 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 footprint. You’ll enjoy opportunities for continued learning and professional development, and an emphasis on employee wellbeing through annual events and team building activities. We value teamwork, respect, and innovation, and we strive to create a positive and supportive work environment for all employees.
How to Apply
To apply for the Clinical Research Coordinator position at Sanford Health, please visit our careers page and submit your application online. Be sure to highlight your relevant skills and experience, and explain why you are interested in this opportunity.
FAQ
- What qualifications are required for this position? A bachelor's degree in a related field and previous experience in clinical research are preferred.
- What are the key responsibilities of a Clinical Research Coordinator? Key responsibilities include coordinating clinical trials, managing data, and ensuring protocol adherence.
- What is the salary range for this position? The estimated salary range is $45,000 to $75,000 per year.
- What benefits does Sanford Health offer? Sanford Health offers a comprehensive benefits package, including health insurance, paid time off, and retirement plan.
- What is the work environment like at Sanford Health? The work environment is collaborative, supportive, and focused on teamwork and innovation.
- What opportunities for career advancement are available? Opportunities for advancement include roles such as Senior Clinical Research Coordinator and Clinical Research Manager.
- Is prior experience in clinical research required? While prior experience is preferred, it is not always required. Strong organizational and communication skills are also highly valued.
- What type of training is provided for this role? Sanford Health provides training on clinical trial protocols, data management systems, and regulatory guidelines.
- What is the typical work schedule for this position? The typical work schedule is 8 Hours - Day Shifts (United States of America).
- What kind of professional development opportunities are there? There are opportunities for continued learning and professional development.
Locations
- Sioux Falls, South Dakota, United States
Salary
49,500 - 82,500 USD / yearly
Source: ai estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Clinical Trial Coordinationintermediate
- Data Managementintermediate
- Patient Recruitmentintermediate
- Regulatory Complianceintermediate
- Informed Consentintermediate
- Source Documentationintermediate
- Case Report Form (CRF) Completionintermediate
- Data Abstractionintermediate
- Specimen Collection and Shippingintermediate
- Protocol Adherenceintermediate
- Deviation Reportingintermediate
- Electronic Data Capture (EDC)intermediate
- Communication Skillsintermediate
- Organizational Skillsintermediate
- Time Managementintermediate
- Problem-Solvingintermediate
- Attention to Detailintermediate
- Medical Terminologyintermediate
- HIPAA Complianceintermediate
- GCP (Good Clinical Practice)intermediate
- ICF (Informed Consent Form)intermediate
- Sponsor Communicationintermediate
- CRO (Contract Research Organization) Communicationintermediate
- Investigator Collaborationintermediate
Required Qualifications
- Bachelor's degree in a related field (e.g., Biology, Nursing, Public Health) (experience)
- Previous experience in clinical research preferred (experience)
- Knowledge of clinical trial regulations and guidelines (e.g., FDA, GCP) (experience)
- Strong understanding of medical terminology (experience)
- Proficiency in data management and analysis (experience)
- Excellent communication and interpersonal skills (experience)
- Ability to work independently and as part of a team (experience)
- Detail-oriented and organized (experience)
- Ability to prioritize and manage multiple tasks (experience)
- Experience with electronic data capture (EDC) systems (experience)
- Familiarity with informed consent procedures (experience)
- Knowledge of HIPAA regulations (experience)
- Ability to maintain patient confidentiality (experience)
- Experience with regulatory submissions (e.g., IRB) (experience)
- Certification in clinical research (e.g., SoCRA, ACRP) preferred (experience)
Responsibilities
- Organize and coordinate various clinical trials.
- Coordinate study-required testing and procedures.
- Coordinate investigational treatment for a variety of conditions and symptoms.
- Participate in clarifying questions and concerns with investigators and sponsors.
- Schedule and coordinate pre-study site visits.
- Monitor enrollment goals and modify recruitment plans as necessary.
- Maintain patient screening/enrollment logs and update sponsors, CROs, and SMOs.
- Ensure completion of all screening, eligibility, and enrollment procedures.
- Conduct interviews to assess subject ability and willingness to follow study procedures.
- Follow randomization procedures per protocol.
- Schedule subjects for follow-up visits.
- Review diaries and questionnaires completed by subjects.
- Ensure appropriate specimen collection, batching, and shipping.
- Collect source documents for sponsor or audit review.
- Assess subject compliance with the test article and follow-up visits.
- Abstract data from medical records and consultation notes.
- Prepare study forms and flow sheets.
- Review inclusion/exclusion criteria to assure subject eligibility.
- Review study protocol, informed consent form, and follow-up procedures with potential subjects.
- Prepare case report forms for sponsor or audit review.
- Manage insurance pre-authorization for study participation.
- Collaborate with physician investigators to ensure safe and compliant treatment.
- Document and maintain all study-related procedures, processes, and events.
- Document protocol deviations and exemptions.
- Record accurate and timely data onto case report forms.
- Maintain source documentation for all case report entries.
- Key in data for electronic submission.
- Correct and edit case report form entries as appropriate.
- Resolve data queries.
- Ensure drug/device accountability by completing appropriate documentation.
Benefits
- general: Comprehensive health insurance (medical, dental, vision)
- general: Paid time off (PTO) and holidays
- general: Retirement plan with employer matching
- general: Life insurance and disability coverage
- general: Flexible spending accounts (FSA) or health savings accounts (HSA)
- general: Employee assistance program (EAP)
- general: Tuition reimbursement or assistance
- general: Professional development opportunities
- general: Employee discounts
- general: Wellness programs
- general: On-site fitness center or gym membership discounts
- general: Childcare assistance or resources
- general: Relocation assistance (if applicable)
- general: Career advancement opportunities within Sanford Health
- general: Supportive and collaborative work environment
- general: Opportunity to contribute to medical advancements
- general: Work-life balance initiatives
- general: Employee recognition programs
- general: Short-term disability
- general: Long-term disability
- general: Voluntary benefits (e.g., supplemental life insurance, accident insurance)
- general: Legal assistance
- general: WFH options (after 6 months)
- general: Lab Coats Provided
- general: Team Building Activities
Tags & Categories
Answer 10 quick questions to check your fit for Clinical Research Coordinator Careers at Sanford Health - Sioux Falls, South Dakota | Apply Now! @ Sanford Health.
Related Books and Jobs