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Clinical Trial Assistant Remote Jobs in Indiana (NOW HIRING)

This is a fully remote, full-time W-2 position. SynergenX is a leader in evidence-based hormone ... This is an exciting opportunity for a compassionate, patient-focused Physician Assistant (PA) or ...

Pre-certification Medical Specialist

Mishawaka, IN · On-site +1

$15.50 - $19.25/hr

Work Location This is a full-time remote opportunity (M-F 8hour shift between 7:30am - 5:30pm ... This role works closely with physicians, clinical staff, insurance carriers, and other healthcare ...

Pre-certification Medical Specialist

Granger, IN · On-site +1

$15.25 - $18.75/hr

Work Location This is a full-time remote opportunity (M-F 8hour shift between 7:30am - 5:30pm ... This role works closely with physicians, clinical staff, insurance carriers, and other healthcare ...

Pre-certification Medical Specialist

South Bend, IN · On-site +1

$16.75 - $20.50/hr

Work Location This is a full-time remote opportunity (M-F 8hour shift between 7:30am - 5:30pm ... This role works closely with physicians, clinical staff, insurance carriers, and other healthcare ...

The Opportunity * Assist in activities associated with regulatory approval of in vitro diagnostic ... This is a hybrid role; remote work arrangements are not available. Relocation assistance is not ...

Showing results 41-60

Clinical Trial Assistant Remote information

See Indiana salary details

$10

$35

$65

How much do clinical trial assistant remote jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical trial assistant remote in Indiana is $35.84, according to ZipRecruiter salary data. Most workers in this role earn between $24.47 and $45.77 per hour, depending on experience, location, and employer.

What is a clinical trial assistant remote?

A Clinical Trial Assistant (CTA) Remote job involves supporting clinical research teams in coordinating, documenting, and managing clinical trials from a remote location. Responsibilities typically include maintaining regulatory documents, tracking study progress, assisting with patient enrollment, and ensuring compliance with protocols and guidelines. CTAs work closely with Clinical Research Associates (CRAs) and Study Managers to facilitate smooth trial operations. Strong organizational skills, attention to detail, and proficiency with clinical trial management systems (CTMS) are essential for success in this role.

What does a clinical trial assistant remote do?

A typical day for a remote Clinical Trial Assistant involves managing and tracking important study documents, supporting site communications, ensuring data accuracy in trial management systems, and assisting with regulatory submissions. You’ll often coordinate with study coordinators, project managers, and other team members via email and virtual meetings to address queries and maintain trial timelines. The role requires a high level of organization and self-motivation, as you’ll balance multiple administrative tasks and respond quickly to shifting priorities. This collaborative and detail-oriented environment provides opportunities to expand your skills in clinical research and prepare for more advanced roles in the field.

What are the key skills and qualifications needed to thrive as a clinical trial assistant remote?

To thrive as a Clinical Trial Assistant Remote, you need a strong foundation in clinical research processes, attention to detail, and familiarity with regulatory compliance, often supported by a degree in life sciences or related field. Proficiency with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of GCP (Good Clinical Practice) guidelines or related certifications is highly beneficial. Excellent organizational skills, proactive communication, and the ability to manage time effectively while working independently are key soft skills. These competencies are crucial for ensuring smooth trial operations, accurate documentation, and effective collaboration with clinical teams from a remote setting.

What are popular job titles related to Clinical Trial Assistant Remote jobs in Indiana?

For Clinical Trial Assistant Remote jobs in Indiana, the most frequently searched job titles are:

Infographic showing various Clinical Trial Assistant Remote job openings in Indiana as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $74,552 per year, or $35.8 per hour.

Experienced Global Study Manager - Clinical Research , Central Labs Services

Labcorp

Indianapolis, IN • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


Labcorp rating

6.6

Company rating: 6.6 out of 10

Based on 1,161 frontline employees who took The Breakroom Quiz

95th of 121 rated laboratories


Job description


Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world's most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you'll have the opportunity to do meaningful work, grow your career and make a real impact on people's health around the world. Together, we're improving health and improving lives.


Labcorp is seeking a remote experienced Global Study Manager to join our Central Labs Services team.

Job Responsibilities:

  • Key contact for clients; Liaison between Clients, CRO, and Labcorp
  • Displays leadership to ensure successful interactions between Labcorp study team members needed to provide seamless study delivery to the client.
  • Provides project management oversight; focusing on key client deliverables through budget, risk, and milestone management.
  • Facilitates communications between Client and extended Labcorp study team, including Study Design Lead and Regional Study Coordinator.
  • Performs review of SOW to ensure quality implementation of client specifics and requirements.
  • Manages a portfolio of global, high-complexity studies.
  • Acts as an ambassador on behalf of the client within Labcorp CLS and across Labcorp business units; exemplifies the concept of Signature Client Service through outstanding, personalized customer service skills
  • Ensures that all customer expectations are documented and acted upon in compliance with regulatory requirements
  • Demonstrates through appropriate self-organization the ability to manage conflicting priorities and to make difficult decisions
  • Able to act efficiently in an environment with dynamic timelines and priorities
  • Accountable for the implementation, monitoring and reporting of performance metrics
  • Actively participates in Labcorp CLS development through continuous process improvement, quality and productivity
  • Work with appropriate internal and external personnel to understand the culture and pipeline of assigned clients
  • Demonstrates strong interpersonal and communication skills that will build strong internal and external relationships to ensure deliverables are on time and within budget
  • Displays appropriate self-organization and ability to manage conflicting priorities
  • Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date
  • Comply with LCLS Global Project Management strategy
  • Support a culture of continuous improvement, quality and productivity
  • Other duties as assigned

Minimum Qualifications:

  • High school diploma or equivalent
  • 5 or more years of experience in pharmaceutical, biotechnology, CRO industry
  • 5 or more years of experience managing complex global clinical projects, including budget, risk, timeline and stakeholder management
  • 5 or more years of experience in client facing (internal and external stakeholder) and stakeholder management.

Preferred Qualifications:

  • Bachelor's degree in life sciences
  • Project Management training or certification (PMP, Prince2)

Additional Job Standards:

  • Proven ability to drive project execution, influence cross-functional teams and deliver results in a dynamic, fast-paced environment
  • Ability to lead client communications confidently, manage expectations, influence outcomes, and build long-term trusted partnerships.
  • Demonstrated leadership skills, including the ability to influence without direct authority, align cross-functional teams, and remove roadblocks.
  • Proven ability to think beyond immediate project tasks and contribute to broader client, operational, and organizational objectives.
  • Customer-focused and solution-oriented approach, with a commitment to delivering exceptional client experience
  • Demonstrated success in process improvement, change management or operational excellence initiatives
  • Excellent understanding of clinical trials, project management methodologies, and clinical development processes.
  • Strong ownership mindset with a demonstrated record of accountability, independent decision-making, and successful execution of complex projects.
  • Proven ability to think strategically, anticipate challenges, and develop proactive solutions that support client and business objectives

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations.

Central Laboratory Services is part of a global contract research organization within Labcorp. We offer the world's largest network of central laboratories and support global clinical trials testing. A common set of processes, procedures, and instrumentation is offered throughout our sites in Europe, Asia/Pacific, and the United States, allowing us to receive samples globally and provide more than 700 assays across all laboratory science disciplines.

Application Window: Closes at the end of the day September 18, 2026.

Pay Range: 60-94K

All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.

Benefits:Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.Employees regularly scheduled to work less than 20 hours, Casual, Intern, and Temporary employees are only eligible to participate in the 401(k) Plan.For more detailed information, pleaseclick here.


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.


We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit ouraccessibility siteor contact us atLabcorp Accessibility. Formore information about how we collect and store your personal data, please see ourPrivacy Statement.



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