Clinical Research Associate (CRA)

Artech Information System LLC

Apply to this job
Woodcliff Lake, NJ, us on site Until 8/21/2026 H-1B sponsor history First posted February 24, 2026 Last posted February 24, 2026
Job description

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

• Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments.

• Participate in development of protocol, case report form, CRF guidelines and other study documents.

• Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal.

• Ensure the training of CROs/investigators on protocol, regulatory, Client SOPs and data issues.

Reviews and approves monitoring reports and ensures tracking of ongoing site issues.

• Minimum of college degree in a relevant discipline.



Bachelors degree in relevant scientific discipline preferred.


• 1-2 years experience in pharmaceutical industry.

Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

 Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 

Office: 973.967.3348 | Fax: 973.998.2599

Connect with us on - LinkedIn | Facebook | Twitter



About this role

Summary

Manage clinical trial operations, oversee site activities, review regulatory documents, ensure protocol adherence.

Job title

Clinical Research Associate (CRA)

Experience level

1-2 years

Industry

healthcare

Location requirements

On-site in Woodcliff Lake, NJ, no remote work

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

degree in relevant disciplineexperience in pharmaceutical industrymanage study protocolsregulatory documentation

Preferred skills

bachelors degree in scientific discipline

Specializations

clinical trialsregulatory documentationmonitoring
Locations

Structured locations inferred from the posting.

Woodcliff Lake, NJ, USA

On-site City