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Full Time Research Investigator Jobs (NOW HIRING)

Prinicipal Investigator

Houma, LA

$45K - $45K/yr

Participate in monitoring visits, audits, and regulatory inspections as required Collaborative Research Model * Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who ...

Prinicipal Investigator

Viera, FL

$43K - $43K/yr

Participate in monitoring visits, audits, and regulatory inspections as required Collaborative Research Model * Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who ...

Prinicipal Investigator

Metairie, LA · On-site

$41K - $42K/yr

Participate in monitoring visits, audits, and regulatory inspections as required Collaborative Research Model * Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who ...

Prinicipal Investigator

Covington, LA · On-site

$40K - $40K/yr

Participate in monitoring visits, audits, and regulatory inspections as required Collaborative Research Model * Supervise and collaborate with full-time mid-level Sub-Investigators (NPs/PAs) who ...

Principal Investigator-Psychiatrist

Garden Grove, CA · On-site

$250K - $350K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... Research also provides highly competitive compensation and a generous benefits package to full time ... The Principal Investigator (PI) is charged to conduct research studies per regulatory, scientific ...

Description FULL TIME RESEARCH ASSOCIATE New York University Tandon School of Engineering The ... The C2SMART Center focuses on academic investigations into metropolitan transit, gridlock ...

Medical Canvass Investigator

Irvine, CA · Remote

$17 - $22/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Research Investigator Job Location : Fully Remote - equipment provided Job Type: Full-Time, Billable Hours, Non-exempt Compensation : $17 - $22/hour, paid weekly Reports To : Regional Manager ...

Sub-Investigator

Chesterfield, MO · On-site

$62.50 - $72.12/hr

  • Medical

  • Dental

  • Vision

  • Retirement

An interest in clinical research and increasing patient access to trials. * Strong clinical ... Additional Requirements The role is a full-time position with regular M-F business hours. Benefits

Associate/Investigator - Immunology

Wauwatosa, WI

$45K - $46K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our ... Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO ...

Civil Rights Investigator

Reno, NV

$46K - $46K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Research Civil Rights laws, regulations, policies, and procedures, and discuss with Director before ... All permanent employees on an annual "A" or "B" contract who are employed at least 50% full-time ...

Associate/Investigator - Immunology

Wauwatosa, WI · On-site

$45K - $46K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are home to the world-renowned Blood Research Institute, we enable life saving gifts from our ... Full-time regular employes are eligible for Medical, Dental, and Vision Plans, Paid Time Off (PTO ...

Showing results 21-40

Full Time Research Investigator information

See salary details

$35K

$56.1K

$101K

How much do full time research investigator jobs pay per year?

As of Aug 18, 2026, the average yearly pay for full time research investigator in the United States is $56,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $47,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Full Time Research Investigator jobs?

Cities with the most Full Time Research Investigator job openings:

What are the most commonly searched types of Research Investigator jobs?

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What states have the most Full Time Research Investigator jobs?

States with the most job openings for Full Time Research Investigator jobs include:

Clinical Research Physician (Principal Investigator/Sub-Investigator) - Full Time

Thermo Fisher Scientific

Richfield, MN • On-site

$48K - $48K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 427 frontline employees who took The Breakroom Quiz

199th of 540 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Location/Division Specific Information:
Trialmed Minneapolis supports biopharmaceutical companies throughout the lifecycle of clinical trials. As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers greater certainty to clinical trial delivery.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
Purpose:
Conducts clinical trials (studies) according to ICH GCP, local regulations, study protocols, and company processes as a principal investigator or sub-investigator. Ensures participant safety, protocol compliance, and data integrity through appropriate medical oversite. Collaborates with site leadership and cross-functional teams to support successful study execution, participant recruitment, enrollment, and retention.
  • Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.
  • Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV) and Investigator meetings as required.
  • Initially functions as a Sub-Investigator and may assume Principal Investigator responsibilities based on study requirements, demonstrated performance, training completion, and site needs.
  • Supports participant recruitment and retention strategies through protocol expertise, community engagement, physician outreach, and collaboration with recruitment teams. Reviews enrollment progress, pre-screening and screening success rates, safety and retention of participants.
  • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
  • Oversees management of investigational medical product (IMP).
  • Oversees multiple studies.
  • Cares for and protects the safety of participants through ethical conduct.
  • Fulfills and complies with all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific and ethical standards.
  • Exercises meticulous attention to detail in recording information and source management.

Education and Experience:
  • MD or DO degree (or equivalent medical degree recognized in the country of practice) with at least 2 years working as a licensed physician.
  • Active, unrestricted medical license in good standing.
  • Exceptional general medical practitioner diagnosis and treatment proficiency.
  • A valid ICH GCP certificate (can be obtained after employment).
  • Prior clinical research experience is preferred but not required. Candidates should possess sufficient clinical expertise and medical judgment to safely conduct protocol-driven clinical research and oversee study participants. Strong clinical backgrounds seeking to transition into clinical research are encouraged to apply.
  • Demonstrated ability to collaborate effectively across a matrixed organization, partnering with clinical operations, recruitment, regulatory, pharmacy, laboratory, and sponsor-facing teams to achieve study objectives.

Knowledge, Skills, and Abilities:
  • Thorough understanding of medical terminology, drug safety, and interpretation of lab reports.
  • Working knowledge of scientific concepts related to the design and analysis of clinical trials.
  • Strong critical thinking, decision making, analytical and problem-solving skills.
  • Comprehensive attention to detail.
  • Capable of learning new processes and systems quickly.
  • Excellent communication, written, verbal and presentation skills.
  • Strong planning, organizational and project management skills.
  • Skilled in Word, Excel, PowerPoint and Internet use.

Working Conditions and Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional travel.

Physical Requirements:
  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movement of both hands.
  • Frequent mobility required.
  • Occasional crouching, stooping, bending and twisting.
  • Light to moderate lifting and carrying up to 15-20 lbs.
  • Ability to use a variety of computer software.
  • Ability to communicate information and ideas effectively, with the ability to listen to, and understand, information and ideas presented through spoken words and sentences.
  • Frequently interacts with others to obtain or relate information to diverse groups.
  • Ability to multitask and perform under stress.
  • Regular and consistent attendance.

Compensation and Benefits
The salary range estimated for this position based in Minnesota is $240,000.00-$315,000.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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