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Fda Contract Jobs in Colorado (NOW HIRING)

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Project Manager

Lakewood, CO · On-site

Contract Length: 6 months+ Client located in Lakewood, Colorado is seeking a Project Manager for a ... Desired Skills: 1) FDA or other regulatory environment. 2) Medical device projects. 3) Six Sigma or ...

OSI Pharmaceuticals

Senior Medical Writer

Boulder, CO · On-site

Writes and/or edits clinical documents for submission to the FDA and other regulatory agencies. Is ... Manages work of contract writers. Develops SOPs and templates for the CTD, protocols, final reports ...

iMPact Business Group

Be Seen First

Test Engineer (Medical Devices)- 27607

Greenwood Village, CO · On-site

$50/hr

... 18 Month + Contract . Our client offers results-driven people a place where they can make a ... Experience with ISO 13485, FDA regulations, or medical device validation. * Familiarity with ...

Certified Group

Courier

Greeley, CO

$19.50/hr

Labstat - A global leader in contract research and testing for nicotine, tobacco, cannabis, hemp ... Complete assigned FDA collections and required photo documentation for warehouse or freezer samples.

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Showing results 21-40

All JobsFda Contract JobsFda Contract Jobs in Colorado

Fda Contract information

See Colorado salary details

$43.1K

$111.5K

$146.2K

How much do fda contract jobs pay per year?

As of Sep 2, 2026, the average yearly pay for fda contract in Colorado is $111,497.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,600.00 and $125,100.00 per year, depending on experience, location, and employer.

What is an Fda contract?

An FDA Contract job refers to a temporary or project-based position working with or for the U.S. Food and Drug Administration (FDA) through a contractual agreement. These roles can be with the FDA directly or through third-party contractors supporting FDA initiatives. Responsibilities may include regulatory compliance, data analysis, scientific research, IT support, or administrative tasks. Contract positions vary in duration and benefits but provide opportunities to work in a highly regulated environment.

What are the primary responsibilities of someone working under an Fda contract?

As an FDA Contract professional, your primary responsibilities usually include developing, reviewing, and managing documents and agreements in accordance with FDA guidelines and regulations. You may coordinate closely with regulatory affairs, legal, and project management teams to ensure that all contract terms support compliance and meet project timelines. Daily tasks might involve drafting and negotiating contract language, tracking deliverables, and supporting regulatory submissions. This role is both detail-oriented and collaborative, and it provides valuable experience for those seeking advancement into regulatory management or specialist positions.

What are the key skills and qualifications needed to thrive in the Fda contract position, and why are they important?

To thrive in an FDA Contract role, you need strong knowledge of FDA regulations, compliance processes, and contract management, often supported by a background in life sciences or regulatory affairs. Familiarity with tools such as Document Control Systems, eCTD publishing software, and experience with regulatory submission platforms are typically required. Outstanding attention to detail, negotiation skills, and the ability to collaborate across cross-functional teams help candidates excel. These competencies are critical for ensuring contracts meet strict regulatory standards and for navigating the complexities of FDA approval and compliance procedures.

What are the most commonly searched types of Fda jobs in Colorado?

The most popular types of Fda jobs in Colorado are:

What are popular job titles related to Fda Contract jobs in Colorado?

For Fda Contract jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Fda Contract jobs in Colorado look for?

The top searched job categories for Fda Contract jobs in Colorado are:

What cities in Colorado are hiring for Fda Contract jobs?

Cities in Colorado with the most Fda Contract job openings:

Fda Contract jobs near you
Infographic showing various Fda Contract job openings in Colorado as of August 2026, with employment types broken down into 80% Full Time, 17% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $111,497 per year, or $53.6 per hour.

Principal Investigator/Clinical Research Rheumatologist position in Denver, CO - Part Time (0-8hr)

ProTouch Staffing

Denver, CO • On-site

$100 - $250/hr

Other

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Research Rheumatologist Physician

Job Type: Full-Time / Part-Time / Contract
Location: Multiple (Denver, CO & Illinois)
Compensation: $100 - $250 per hour (based on experience, contract type, and role)
Schedule: Flexible | Part-Time (0-8 hours/week) or Full-Time options

Job Summary

We are seeking a board-certified Rheumatologist to serve as a Clinical Research Physician. This is an excellent opportunity for physicians passionate about advancing medicine through clinical research while maintaining a flexible schedule.

Key Responsibilities

  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on rheumatology clinical trials.

  • Conduct medical screenings, physical examinations, and specialty-specific evaluations for study participants.

  • Provide medical oversight and ensure patient safety throughout all trial phases.

  • Monitor, document, and report adverse events (AEs/SAEs) per protocol and regulatory standards.

  • Collaborate with study coordinators, research staff, sponsors, CROs, and IRBs to ensure compliance and high-quality data.

  • Participate in site initiation visits, monitoring visits, audits, and investigator meetings.

  • Contribute to protocol feasibility reviews, recruitment strategies, and study design discussions.

  • Maintain compliance with GCP, FDA regulations, and institutional guidelines.

  • Stay updated on clinical research practices and therapeutic advancements in rheumatology.

Requirements

  • MD or DO degree with an active, unrestricted U.S. medical license (CO and/or IL preferred).

  • Board certification in Rheumatology.

  • DEA license and BLS/ACLS certification preferred.

  • Prior experience in clinical research strongly preferred (training available for motivated candidates).

  • Proficiency with EHR, EDC, CTMS, and medical documentation systems.

  • Strong communication and interpersonal skills; ability to work in a multidisciplinary, fast-paced environment.

  • Commitment to ethical research and patient-centered care.

Compensation & Benefits

  • $100 - $250 per hour (based on experience, contract type, and role).

  • Flexible scheduling (0-8 hours/week part-time or full-time).

  • Opportunity to participate in cutting-edge clinical trials in rheumatology.

  • Professional growth in research leadership and investigator experience.

Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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