Top 12 Clinical specialist Jobs in Sioux Falls Sd

Clinical Research Coordinator OR Research Specialist
Avera —Sioux Falls, SD
- $21.75 - $36.50 an hour
- Online Application
- Vital signs
- OSHA
- Mid-level
- Paid time off
MDS Solutions - Clinical Reimbursement Specialist
MDS Solutions —Sioux Falls, SD
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- HIPAA
- Health savings account
- Dental insurance
Therapy Clinical Consultant
Good Samaritan —Sioux Falls, SD
- $43 - $71 an hour
- Online Application
- Background check
- 5 years
- Pass drug screening
- Health insurance
- Dental insurance
Quick Apply
Clinical Customer Service Specialist
Neighborhood Dental —Sioux Falls, SD
- $21 - $28 an hour
- Full-time
- Dental office
- HIPAA
- Mid-level
- Profit sharing
- Continuing education credits
Quick Apply
9d
Registered Nurse (RN) | Clinical Documentation Specialist
Avera —Sioux Falls, SD
- $31.00 - $46.25 an hour
- Online Application
- OSHA
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- Hospital
- Paid time off
17h
Clinical Informatics Analyst | Ancillary/Procedural Endoscopy
Avera —Sioux Falls, SD
- $63,960 - $96,200 a year
- Online Application
- Surgery
- OSHA
- RN License
- Paid time off
10d
Clinical Quality Specialist - Canton Medical Center - Full Time
Sanford Health —Canton, SD
- $24.00 - $38.50 an hour
- Online Application
- Background check
- Nursing
- RN License
- Health insurance
- Dental insurance
Quick Apply
Optometrist
Visionworks —Sioux Falls, SD
- Full-time
- Private practice
- Mid-level
- Vision insurance
Quick Apply
Pediatric Clinical Psychologist - Feeding/Swallowing Disorders
LifeScape —Sioux Falls, SD
- $41.90 - $62.86 an hour
- Choose your own hours
- Background check
- Pass drug screening
- Mid-level
- Loan forgiveness
- Flexible schedule
Quick Apply
7h
Hospital - Clinical Pharmacist Specialist (Bone Marrow Transplant)
UT Health Science Center at San Antonio —United States
- Hospital
- Outpatient experience
- 3 years
Quick Apply

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Clinical Research Coordinator OR Research Specialist

Avera -
Sioux Falls, SD

Apply Now

Job Details

Full-time
$21.75 - $36.50 an hour

Benefits

Paid time off

Qualifications

Laboratory sample storage
Collaborate with healthcare professionals
TJC
Laboratory project records management
Centrifugation
Laboratory inventory control
Vital signs
Informed consent
OSHA
Research ethical considerations
Adverse event reporting
Clinical incident reports
Safety regulations
CMS
Care documentation
Mid-level
Medical scheduling
Research project coordination
Data integrity and documentation
Collecting samples for laboratory testing
Records management
Clinical data entry
Research safety & compliance
Laboratory standard operating procedures
Informed consent procedures implementation
Medical laboratory work experience
Compliance documentation
Public health
Research compliance clinical trial records management
Trade school

Full Job Description

Location:

Avera Research 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.

$21.75 - $36.50

Position Highlights

This position may include travel.

For this position, we will hire either a Clinical Research Coordinator or a Research Specialist.

Clinical Research Coordinator Pay Range: $24.00 - $36.50
Research Specialist Pay Range: $21.75 - $33.00

Clinical Research Coordinator Brief Overview

An advanced position that contributes to the overall operations of one or more research studies. The CRC is responsible for implementation of the study protocol, recruitment plan, study visits, data, study assessments, and other tasks outlined in the protocol. This position requires close collaboration with the study team and investigator to ensure safe and compliant research procedures and follow-up per the established research protocol. This position will work directly with research participants, physicians, nurses, community stakeholders, and health/social service organizations. This position has opportunities for ongoing learning and contribution to research that is focused on improving health and wellbeing of individuals and the community.

Required Education, License/Certification, or Work Experience:

Bachelor's From a four year college or university within the health and science field

Research Specialist Brief Overview

Works under general direction to perform professional level medical or scientific research assignments related to particular or specialized field of endeavor. Performs diverse and complex duties including, collection, processing and shipment of research specimens to local or reference labs, entering patient data into a variety of web based data capture systems, analysis, scheduling and conduct of daily research activities, retention and organization of documentation, and consenting subjects to nontreatment clinical trials.

Required Education, License/Certification, or Work Experience:

Associate's or equivalent from a 2 college or technical school or a minimum of 1 of clinical research experience or equivalent combination of education and work related experience.

POSITION HIGHLIGHTS

This position may support multiple types of research projects at Avera Research Institute, including observational studies and clinical trials. Research areas may include maternal and child health, public health, clinical research, and other studies involving varied patient populations across multiple health conditions.

This position may include supporting the ECHO study, Environmental influences on Child Health Outcomes, a longitudinal, observational study following pregnant women and their children to better understand how environmental exposures during the prenatal and early childhood time frame affect health outcomes for children later in life.

The position may also support clinical trial activities across a variety of research areas. Responsibilities may include patient screening, recruitment and enrollment, data collection and management, study assessments, lab draws, EKGs, vital signs, study drug injections, patient education, and maintaining study records in an electronic database. The individual may also help ensure compliance with study protocols and regulatory requirements while working closely with a multidisciplinary team, including pharmacy, principal investigators, sponsors, and other research partners.

We are seeking individuals who have a strong interest in working with diverse patient populations and research participants across multiple disease states and areas of research. This may include pregnant women, children, and patients participating in observational studies or clinical trials. Ideal candidates will have an interest in public health, maternal and child health, clinical research, and supporting research that advances health outcomes across a variety of populations.

Learn more about the Avera Research Institute at the link below:
https://www.avera.org/research-and-clinical-trials/research-institute/

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

An advanced position that contributes to the overall operations of one or more research studies. The CRC is responsible for implementation of the study protocol, recruitment plan, study visits, data, study assessments, and other tasks outlined in the protocol. This position requires close collaboration with the study team and investigator to ensure safe and compliant research procedures and follow-up per the established research protocol. This position will work directly with research participants, physicians, nurses, community stakeholders, and health/social service organizations. This position has opportunities for ongoing learning and contribution to research that is focused on improving health and wellbeing of individuals and the community. This position may include travel.

What you will do

Coordinates research studies per Good Clinical Practices guidelines, FDA regulations, and approved protocols.
Understands and adheres to Standard Operating Procedures (SOPs). Ability to develop or improve SOPs, help guides, and other team resources.
Acquires detailed knowledge of assigned research protocols and ability to conduct study required processes, procedures, and assessments. Ability to prepare, utilize, and review Case Report Forms. Collects and manages data, Case Report Forms, and timely entry into the electronic data capture system.
Collects and assists with processing all laboratory specimens to include centrifuging, separating, measuring, storing, shipping, and distributing to appropriate testing areas. Maintains inventory of laboratory supplies and study kits.
Screens, recruits, and enrolls study participants using study’s eligibility criteria. Preforms the informed consent, answering all participant questions, and obtaining appropriate sign-off.
Ensures the adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data.
Ensures validity of research results by ensuring timely, accurate, and complete data documentation, reporting deviations, violations, and serious adverse events.
Develops relationships with referring physicians, clinical staff, and ancillary departments to facilitate compliance with and accrual to clinical trials.

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 From a four year college or university within the health and science field

Preferred Education, License/Certification, or Work Experience:

1-3 years Human Research
1-3 years Laboratory or clinical

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.

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 [email protected] .

Apply Now

Refine Your Search

clinical specialist jobs in sioux falls sd

Clinical Research Coordinator OR Research Specialist

MDS Solutions - Clinical Reimbursement Specialist

Therapy Clinical Consultant

Clinical Customer Service Specialist

Registered Nurse (RN) | Clinical Documentation Specialist

Clinical Informatics Analyst | Ancillary/Procedural Endoscopy

Clinical Quality Specialist - Canton Medical Center - Full Time

Optometrist

Pediatric Clinical Psychologist - Feeding/Swallowing Disorders

Hospital - Clinical Pharmacist Specialist (Bone Marrow Transplant)

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Explore jobs in cities nearby

I want to receive the latest job alert for clinical specialist in sioux falls sd

Explore jobs in more locations

This position may include travel.

For this position, we will hire either a Clinical Research Coordinator or a Research Specialist.

Clinical Research Coordinator Brief Overview

Research Specialist Brief Overview

Learn more about the Avera Research Institute at the link below:
https://www.avera.org/research-and-clinical-trials/research-institute/

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clinical specialist jobs in sioux falls sd

Discover related jobs

Explore jobs in cities nearby

I want to receive the latest job alert for clinical specialist in sioux falls sd

Explore jobs in more locations

This position may include travel.

For this position, we will hire either a Clinical Research Coordinator or a Research Specialist.

Clinical Research Coordinator Brief Overview

Research Specialist Brief Overview

Learn more about the Avera Research Institute at the link below: https://www.avera.org/research-and-clinical-trials/research-institute/

Learn more about the Avera Research Institute at the link below:
https://www.avera.org/research-and-clinical-trials/research-institute/