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Tmf Associate Jobs in Minnesota (NOW HIRING)

Sr Clinical Research Spec

MN · On-site +1

$50 - $55/hr

Advanced knowledge of clinical trial management systems (CTMS), electronic data capture (EDC), and trial master file (TMF). * Experience with Good Clinical Practice (GCP). * Preferred: Knowledge of ...

Tmf Associate information

See Minnesota salary details

$16

$39

$68

How much do tmf associate jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for tmf associate in Minnesota is $39.16, according to ZipRecruiter salary data. Most workers in this role earn between $31.54 and $43.08 per hour, depending on experience, location, and employer.

What is the difference between Tmf Associate vs Tmf Analyst?

AspectTmf AssociateTmf Analyst
Required CredentialsBachelor's degree in life sciences, pharmacy, or related fields; basic knowledge of clinical trial processesBachelor's or master's degree; deeper understanding of TMF processes and regulatory requirements
Work EnvironmentClinical research organizations, pharmaceutical companies, or CROs; supporting TMF documentationMore analytical role within similar settings; involved in reviewing and ensuring compliance
Employer & Industry UsageCommonly used in clinical trial documentation teamsUsed in quality assurance and compliance teams within the same industry

The main difference between a Tmf Associate and a Tmf Analyst lies in their experience level and scope of responsibilities. Tmf Associates typically handle documentation support and basic compliance tasks, while Tmf Analysts perform more detailed reviews and analysis to ensure regulatory adherence. Both roles are essential in clinical trial management, with the Analyst position requiring a deeper understanding of TMF processes.

What are popular job titles related to Tmf Associate jobs in Minnesota? For Tmf Associate jobs in Minnesota, the most frequently searched job titles are:
Sr Clinical Research Spec

Sr Clinical Research Spec

Lancesoft

MN • On-site, Remote

$50 - $55/hr

Full-time

Posted 8 days ago


Job description

Job Description
Join our team as a Senior Clinical Research Specialist and be at the forefront of driving clinical trial timelines and innovations. This role offers the unique opportunity to work remotely from Virtual, MN, providing flexibility and work-life balance while contributing to groundbreaking clinical research.
Key Responsibilities
  • Oversee, design, plan, and develop clinical evaluation research studies.
  • Prepare and author protocols and patient record forms.
  • Conduct registered and non-registered clinical studies of products that meet medical needs or offer commercial potential.
  • Oversee and interpret results of clinical investigations for new drug, device, or consumer applications.
  • Resolve operational aspects of clinical trials in conjunction with project teams, adhering to SOPs, GCP, and specific country regulations.
  • Prepare clinical trial budgets and may be responsible for clinical supply operations, site, and vendor selection.
Qualifications
  • Bachelor's degree required.
  • Minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience.
  • Advanced knowledge of clinical trial management systems (CTMS), electronic data capture (EDC), and trial master file (TMF).
  • Experience with Good Clinical Practice (GCP).
  • Preferred: Knowledge of diabetes therapy and audit experience.
Key Competencies
  • Autonomy: Work independently under limited supervision, developing approaches to solutions.
  • Organizational Impact: Responsible for entire projects or processes, contributing to work group objectives.
  • Innovation and Complexity: Address complex problems requiring an understanding of multiple issues and specialties.
  • Communication and Influence: Communicate effectively with senior internal and external customers and vendors.
  • Leadership and Talent Management: Provide guidance, coaching, and training to other employees within the job area.

This is an exciting opportunity to be part of a dynamic team, driving innovation and excellence in clinical research. Apply today and make a significant impact on the future of healthcare.
Meet Your Recruiter
Balaji R

LanceSoft logo

About LanceSoft

Sourced by ZipRecruiter

Established in 2000, LanceSoft is a Certified MBE and Woman-Owned organization. Lancesoft Inc. is one of the highest rated companies in the industry. We have been recognized as one of the Largest Staffing firms and ranked in the top 50 fastest Growing Healthcare Staffing firms in 2022. Lancesoft offers short- and long-term contracts, permanent placements, and travel opportunities to credentialed and experienced professionals throughout the United States. We pride ourselves on having industry leading benefits. We understand the importance of partnering with an expert who values your needs, which is why we're 100% committed to finding you an assignment that best matches your career and lifestyle goals. Our team of experienced career specialists takes the time to understand your needs and match you with the right job Lancesoft has been chosen by Staffing Industry Analysts as one of the Best Staffing Firms to Work for.LanceSoft specializes in providing Registered Nurses, Nurse Practitioners, LPNs/LVNs, Social Workers, Medical Assistants, and Certified Nursing Assistants to work in Acute Care Centers, Skilled Nursing Facilities, Long-Term Care centers, Rehab Facilities, Behavioral Health Centers, Drug & Alcohol Facilities, Home Health & Community Health, Urgent Care Clinics, and many other provider-based facilities.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Herndon, VA, US

Year founded

2000

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