Clinical Research Specialist

Integrated Resources INC

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Mounds View, MN, us on site Until 8/21/2026 H-1B sponsor history First posted February 23, 2026 Last posted February 23, 2026
Job description


INTEGRATED RESOURCES STAFFING PVT LTD

Job Title: Clinical Research Specialist

Location: Mounds View, MN
Duration: 6 + months (Possibility of extension)

Local candidate needed on site.

Top 3 things CSH is looking for:
1. Clinical trial experience
2. Site Management experience
3. Medical Device experience

DESCRIPTION:

· Coronary Structural Heart Clinical is looking for an enthusiastic, motivated candidate to be a contract Clinical Research Specialist in our dynamic environment.

· The incumbent has responsibility for meeting the milestones of a clinical study in compliance with applicable clinical and regulatory standards and in alignment with the Study Manager as well as business needs.

· Work is completed under general direction.

Travel: N/A
Site: USA-MN-Mounds View
Shift Type: First

POSITION RESPONSIBILITIES

• Oversight of a clinical study including enrolment, long-term follow-up, trial master file maintenance and study activation phases.
• Ensure site compliance in regulatory requirements in regards to tracking site activation documents and ongoing study files by performing study file audits.
• Track device accountability reconciliation.
• Evaluate protocol deviation data during the conduct of the study and for completion of clinical study deviation trending requirements.
• Prepare weekly study reports and record meeting minutes.
• Assist in planning, coordination and preparation of meeting materials for investigator meetings.
• Regularly communicates study status to management.

BASIC QUALIFICATIONS
• Bachelor's Degree in a scientific field of study.
• Working knowledge of Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials.
• Minimum 3 years' experience directly supporting clinical research or relevant experience in medical/scientific area.
• Master's degree will substitute for 1 year of experience. PhD or MD will substitute for 2 years of experience.
• Strong written, oral, and interpersonal communication skills including proficient knowledge of medical terminology.
• Computer skills (MS Office products, word processing, spreadsheets, etc.).
• High attention to detail and accuracy.
• Ability to manage multiple tasks.
• Good prioritization and organizational skills.
• Excellent problem solving skills
• Positive outlook.
• Flexible and dependable.
• Works effectively on cross-functional teams.
• Presents professional manner and appearance


We do have referral bonus of $500 per candidate, if you refer any of your friends or colleague who are looking out for the same job.


Thanks & Regards,

Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # - 732 – 318 -6506 | (W) # 732-549-2030 – Ext – 324 | (F) 732-549-5549
Email id – seema @irionline.com| www.irionline.com 
LinkedIn: https://in.linkedin.com/in/seemachawhan

About this role

Summary

Manage clinical study milestones, ensure compliance, oversee site activities, and coordinate documentation.

Job title

Clinical Research Specialist

Experience level

3+ years

Industry

healthcare

Location requirements

On-site in Mounds View, MN, USA, no remote work allowed.

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

clinical trial experiencesite managementmedical device experienceGCPregulatory compliancecommunicationMS Office

Preferred skills

None specified

Specializations

clinical trialssite managementmedical device
Locations

Structured locations inferred from the posting.

Mounds View, MN 55112, USA

On-site City