Top 14 Research & development laboratory Jobs in Independence, Ia

Clinical Research Coordinator II
Iterative Health —Waterloo, IA
- Patient monitoring
- HIPAA
- Mid-level
Quick Apply
Emergency Medical Technician - Basic
Biolife Plasma Services —Waterloo, IA
- Full-time
- CPR Certification
- Nursing
- BLS Certification
- Paid training
- Health savings account
Quick Apply
6d
Medical Lab Technician - Nights
MercyOne —Oelwein, IA
- Full-time
- Adults
- Mid-level
- Adolescents
Quick Apply
6d
Laboratory Technical Associate-Main Laboratory
UnityPoint Health —Waterloo, IA
- Full-time
- Word processing
- Computer literacy
- English
- Paid holidays
- Disability insurance
Lab Assistant/Phlebotomist FT Days
MercyOne —Waterloo, IA
- Full-time
- Computer literacy
- Internal Medicine
- Adults
Lab Quality Coordinator MLS
MercyOne —Waterloo, IA
- Weekends as needed
- Mid-level
- 3 years
- Master's degree
6d
Laboratory Supervisor
Microbac —Waterloo, IA
- Full-time
- Management
- Pass drug screening
- Ability to lift 50 pounds
- Wellness program
- Paid holidays
Quick Apply
EMT-Basic (EMT-B) – Plasma Center
Biolife Plasma Services —Waterloo, IA
- $20.00 - $29.26 an hour
- Full-time
- CPR Certification
- Nursing
- LVN
- Paid holidays
- Disability insurance
6d
Medical Assistant I-Phlebotomist
UnityPoint Health —Waterloo, IA
- From $16.97 an hour
- Part-time
- Nursing home
- Word processing
- Computer literacy
- Paid holidays
- Disability insurance
Medical Assistant II/Phlebotomist-Laboratory
UnityPoint Health —Waterloo, IA
- $17.02 an hour
- 8 hour shift
- Nursing home
- Word processing
- Computer literacy
- Paid holidays
- Disability insurance
RN-Cath Lab
UnityPoint Health —Waterloo, IA
- Weekends as needed
- Nursing
- RN License
- Hospital
- Paid holidays
- Disability insurance

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Micro Specialist
BrewDog USA Inc —Canal Winchester, OH
Independent reading on industry relevant technical papers and developments. Ability to train and mentor junior lab technicians on learning fundamental lab tasks…
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Lab Services Coordinator - Clinical Trials Processing Lab
The Ohio State University Wexner Medical Center —Columbus, OH
Participates in data entry and management, quality control, audits and FDA inspections, continuous quality improvement and inventory management of clinical…

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Clinical Research Coordinator II

Iterative Health -
Waterloo, IA

Quick Apply

Job Details

Qualifications

Data collection

Full Job Description

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.

We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.

As a Clinical Research Coordinator II (CRC II) at Iterative Health you will play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.

This role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.

Where You'll Drive Impact

Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision
Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements
Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy
Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines
Serve as a primary point of contact for study participants throughout study participation
Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues
Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
Review safety reports and ensure appropriate investigator review and documentation in a timely manner
Maintain inventory and organization of study equipment, supplies, and investigational products onsite
Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience
Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
Maintain compliance with all site SOPs, privacy standards, and research protocols
May support onboarding and mentorship of junior research staff and coordinators
Perform job related duties as requested

What You Bring to the Team

Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
3-5 years of clinical research or healthcare experience required
CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred
Strong organizational skills and attention to detail
Ability to manage competing priorities in a fast-paced environment
Ability to read, interpret, and apply research protocols and clinic policies
Proficiency with CTMS, EDC systems, and standard office software applications
Familiarity with CTMS or EDC systems preferred

Physical Requirements

Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
Ability to lift and move up to 25 pounds as needed

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact [email protected].

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Refine Your Search

research & development laboratory jobs in independence, ia

Clinical Research Coordinator II

Emergency Medical Technician - Basic

Medical Lab Technician - Nights

Laboratory Technical Associate-Main Laboratory

Lab Assistant/Phlebotomist FT Days

Lab Quality Coordinator MLS

Laboratory Supervisor

EMT-Basic (EMT-B) – Plasma Center

Medical Assistant I-Phlebotomist

Medical Assistant II/Phlebotomist-Laboratory

RN-Cath Lab

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