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Trial Interactive Jobs (NOW HIRING)

TScan Therapeutics

TMF Coordinator

Waltham, MA

$87K - $93K/yr

Support day-to-day Trial Master File (TMF) activities for clinical studies, which includes ... To begin an interactive dialogue with TScan regarding a reasonable accommodation in connection with ...

TScan Therapeutics

TMF Coordinator

Waltham, MA

$87K - $93K/yr

Support day-to-day Trial Master File (TMF) activities for clinical studies, which includes ... To begin an interactive dialogue with TScan regarding a reasonable accommodation in connection with ...

TScan Therapeutics

TMF Coordinator

Waltham, MA · On-site

$87K - $93K/yr

Support day-to-day Trial Master File (TMF) activities for clinical studies, which includes ... To begin an interactive dialogue with TScan regarding a reasonable accommodation in connection with ...

Exelixis

Clinical Supplies Manager II

Alameda, CA · On-site

$132K - $188K/yr

Represent clinical supplies function at clinical trial team meetings; communicate plan and ... Knowledge of Interactive Voice/Web response systems for use in clinical studies. * Working ...

Exelixis

Clinical Supplies Manager II

Alameda, CA · On-site

$132K - $188K/yr

Represent clinical supplies function at clinical trial team meetings; communicate plan and ... Knowledge of Interactive Voice/Web response systems for use in clinical studies. * Working ...

Exelixis

Clinical Supplies Manager II

Alameda, CA

$132K - $188K/yr

Represent clinical supplies function at clinical trial team meetings; communicate plan and ... Knowledge of Interactive Voice/Web response systems for use in clinical studies. * Working ...

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Trial Interactive information

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$17

$39

$70

How much do trial interactive jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for trial interactive in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What are Trial Interactive professionals?

Trial Interactive professionals are specialists who work with the Trial Interactive platform, a cloud-based solution designed for managing clinical trials. They help pharmaceutical and biotechnology companies streamline clinical document management, electronic trial master files (eTMF), and regulatory compliance. Their role often includes implementing, maintaining, and supporting the software to ensure that clinical trial data is secure, organized, and audit-ready. These professionals typically have experience in clinical research, document management, and regulatory standards such as GCP (Good Clinical Practice).

Does TransPerfect own trial interactive?

Trial Interactive is a separate company that provides eDiscovery and litigation support services. TransPerfect does not own Trial Interactive, although both companies operate within the legal and translation industries. Each company functions independently with its own management and service offerings.

What is the difference between Trial Interactive vs Clinical Research Coordinator?

AspectTrial InteractiveClinical Research Coordinator
Primary RoleManages and facilitates electronic trial data and patient engagement toolsCoordinates clinical trial activities, patient visits, and data collection
Required CredentialsOften requires knowledge of clinical trial software, basic healthcare backgroundTypically requires nursing or healthcare-related certifications
Work EnvironmentRemote or office-based, technology-focusedHospital, clinic, or research facility
Industry UsageUsed across pharmaceutical, biotech, and clinical research companiesCommonly employed in hospitals, research centers, and clinical sites

While both roles are involved in clinical trials, Trial Interactive focuses on managing electronic trial data and patient engagement tools, often in a remote or tech-driven environment. In contrast, a Clinical Research Coordinator handles on-site trial activities, patient interactions, and data collection, usually within healthcare facilities. Understanding these differences helps in choosing the right career path or job search focus.

What is a CTA in clinical trials?

A CTA, or Clinical Trial Application, is a submission made by a sponsor or investigator to regulatory authorities to gain approval to conduct a clinical trial. It includes detailed information about the study design, safety measures, and participant protections, and is a key document for trial approval and compliance. Trial professionals often review and prepare CTAs as part of their regulatory responsibilities.

What qualifications do you need to work in clinical trials?

To work in clinical trials, candidates typically need a relevant educational background such as a degree in life sciences, healthcare, or related fields. Additional qualifications may include knowledge of Good Clinical Practice (GCP), familiarity with clinical trial protocols, and sometimes certification in clinical research or related areas. Strong organizational skills and attention to detail are also important for roles in this field.

How much does a clinical trial assistant earn?

A clinical trial assistant typically earns between $40,000 and $60,000 annually, depending on experience, location, and the size of the organization. Entry-level positions may start lower, while experienced assistants with specialized skills can earn higher salaries. The role often requires familiarity with clinical trial protocols and regulatory requirements.

What are some typical challenges faced by professionals working in a Trial Interactive role within clinical research?

Professionals in a Trial Interactive role often manage complex documentation and data workflows for clinical trials, which can involve coordinating with multiple stakeholders across different time zones. Common challenges include ensuring compliance with regulatory requirements, maintaining data integrity, and adapting to rapidly changing study protocols. Additionally, tight timelines and the need for clear communication with clinical teams, sponsors, and regulatory authorities require strong organizational and collaboration skills. Overcoming these challenges provides valuable experience and can open doors to more advanced roles in clinical operations or project management.

What are the key skills and qualifications needed to thrive as a Trial Interactive Specialist, and why are they important?

To thrive as a Trial Interactive Specialist, you need a background in clinical research, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic trial master file (eTMF) systems, clinical trial management systems (CTMS), and relevant certifications such as GCP are typically required. Strong attention to detail, organizational skills, and effective communication set top performers apart in this role. These skills ensure accurate documentation, regulatory adherence, and seamless coordination in clinical trial operations.
Infographic showing various Trial Interactive job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 90% Full Time, 7% Part Time, 1% Temporary, and 1% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Study Start-Up Coordinator- PharmD

Study Start-Up Coordinator- PharmD

Medpace, Inc.

Cincinnati, OH • On-site

Other

Medical, PTO

Posted 27 days ago

Medpace rating

8.4

Company rating: 8.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

15th of 57 rated research

Job description

Job Summary
Our clinical operations activities are growing rapidly, and we are currently seeking full-time, office-based Regulatory Submissions Coordinators to join our Study Start-up team. This position works both independently and collaboratively with a team to meet common goals and plays a key role in the clinical trial management and study start-up process at Medpace. We are seeking entry level employees. If you want an exciting career where you can build a foundation in industry knowledge through our robust training program and develop and grow your career even further, then this is the opportunity for you.
Responsibilities
  • Communicate with research sites (doctor's offices, universities, hospitals, etc.) to collect all essential documents required before the site begins to screen patients to participate in the clinical trial;
  • Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
  • Collect, review, organize, and assemble regulatory start-up submissions (including submissions to Institutional Review Boards (IRB);
  • Maintain timelines for study start-up through both internal and external collaboration; and
  • Review pertinent regulations and guidance to develop proactive solutions to regulatory issues and challenges.

SITE ACTIVATION & MAINTENANCE (SAM) TRAINING PROGRAM
Medpace training programs are curated to educate and support experienced associates, as well as those that are new to the industry. The SAM Training Program embraces evidence- based learning & development models to advance professional learning and employee performance. In the program, you will...
• Complete independent learning modules, interactive exercises, and team workshops through the core curriculum;
• Gain exposure to real-world tasks through a robust mentoring program; and
• Join other professionals revolutionizing efficient and seamless study start-up to advance clinical trials.
Qualifications
  • A minimum of a PharmD is required (preferably in a Life Sciences field);
  • 3.5 GPA and above preferred;
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office; and
  • Great attention to detail and excellent oral and written communication skills.

Travel: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
  • Cincinnati Campus Overview
  • Flexible work environment
  • Competitive PTO packages, starting at 20+ days
  • Competitive compensation and benefits package
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives
  • Community involvement with local nonprofit organizations
  • Discounts on local sports games, fitness gyms and attractions
  • Modern, ecofriendly campus with an on-site fitness center
  • Structured career paths with opportunities for professional growth
  • Discounted tuition for UC online programs

Awards
  • Named a Top Workplace in 2024 by The Cincinnati Enquirer
  • Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
  • Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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