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Trials Manager Jobs in Indiana (NOW HIRING)

Powers Health

Manager Sourcing

Munster, IN

Supports Value Analysis Committees focused on new product introductions, product trials and overall product/service change initiatives with Value Analysis. * Monitors supplier performance and manages ...

Powers Health

Manager Sourcing

Munster, IN · On-site

$43.45 - $68.50/hr

Supports Value Analysis Committees focused on new product introductions, product trials and overall product/service change initiatives with Value Analysis. * Monitors supplier performance and manages ...

Fitesa Simpsonville, Inc.

Sr. Process Engineer

Terre Haute, IN · On-site

$99K - $128K/yr

Managing the trials, creating detailed trial plans, follow up and analyzing the trial results. * Design of Experiments and Statistical Analysis. * Continuous monitoring and improvement of the product ...

Fitesa Simpsonville Inc.

Sr. Process Engineer

Terre Haute, IN · On-site

$99K - $128K/yr

Managing the trials, creating detailed trial plans, follow up and analyzing the trial results. * Design of Experiments and Statistical Analysis. * Continuous monitoring and improvement of the product ...

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Trials Manager information

What are the key skills and qualifications needed to thrive as a trials manager, and why are they important?

To thrive as a Trials Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a relevant scientific degree and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and often certifications like ACRP or SOCRA are highly valuable. Strong leadership, organization, and communication skills help manage multidisciplinary teams and ensure protocol adherence. These competencies are crucial for delivering safe, efficient, and compliant clinical trials that advance medical research.

What is a trials manager?

Trials Managers are professionals responsible for overseeing and coordinating clinical trials or research studies. They manage all aspects of the trial process, including planning, organizing, and ensuring that studies are conducted in accordance with regulatory guidelines and protocols. Their role often involves liaising with sponsors, investigators, and regulatory authorities, as well as monitoring progress and reporting results. Trials Managers play a key role in ensuring that trials are completed on time, within budget, and to the required quality standards.

What are the main challenges a trials manager faces when coordinating multi-site clinical trials?

As a Trials Manager, one of the primary challenges when overseeing multi-site clinical trials is ensuring consistent protocol adherence and data quality across all locations. This involves frequent communication with site staff, troubleshooting logistical issues, and monitoring regulatory compliance. Additionally, balancing timelines and resources while managing diverse teams can be demanding. Successful Trials Managers proactively address these challenges through robust planning, regular site visits, and clear documentation to keep studies on track.

What is the difference between Trials Manager vs Clinical Research Coordinator?

CriteriaTrials ManagerClinical Research Coordinator
Required CredentialsBachelor's degree, experience in trial management, knowledge of regulationsBachelor's degree, clinical research experience, regulatory knowledge
Work EnvironmentOversees multiple trials, manages teams, coordinates with sponsorsHandles daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, clinics, research institutions

The Trials Manager focuses on overseeing entire clinical trials, managing teams, and ensuring compliance across multiple studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, working directly with patients and collecting data. Both roles require similar educational backgrounds and regulatory knowledge but differ in scope and responsibilities.

What are popular job titles related to Trials Manager jobs in Indiana? For Trials Manager jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Trials Manager jobs in Indiana look for? The top searched job categories for Trials Manager jobs in Indiana are:
What cities in Indiana are hiring for Trials Manager jobs? Cities in Indiana with the most Trials Manager job openings:
Trials Manager jobs near you
Infographic showing various Trials Manager job openings in Indiana as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Clinical Development Trial Lead Assoc Dir

Globalchannelmanagement

Indianapolis, IN • On-site

Full-time

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

Job description

Clinical Development Trial Lead Assoc Dir requires:

  • Stamford, CT or Indianapolis, IN
  • 5+ years clinical research experience or relevant experience in a scientific or health-related field
  • Experience with oncology (early & late phase clinical trials)
  • Applied knowledge of project management methodology, processes and tools
  • Demonstrated ability to lead and work effectively cross-culturally with global colleagues and with TPOs
  • Be recognized as a leader with demonstrated ability to coach others in process expertise.
  • Embrace strategic organizational changes and lead others effectively through these, exhibiting flexibility to adjust quickly and effectively to frequent change and altered priorities
  • Ability to influence without authority
  • Previous experience working in cross-functional teams/ projects and/or ability to establish and maintain relationships Effective and influential communication, self-management, and organizational skills
  • Demonstrated ability to handle complex situations through problem-solving, critical thinking and navigating ambiguity Other Information/Additional
  • Minimum of 5 years clinical trial experience with a strong working knowledge of the clinical research process
  • Prior clinical trial site-level or affiliate experience
  • Prior experience with local/country regional requirements
  • Strong analytical skills Proficiency in use of project management tools and techniques (e.g., Critical Chain, Veeva, MS Project, MS Excel, MS PowerPoint, PowerBI)
  • Need to travel periodically to scientific/regional meetings
  • Associate Director, Clinical Development Trial Lead (CDTL)
  • Clinical Trial Process Leadership and Expertise
  • Leverage and demonstrate broad understanding of therapeutic, clinical drug development, and process expertise in order to influence study design and program-level decisions considering regional needs.
  • Recognize inter-relatedness of cross-functional activities and understand the impact of project decisions on the overall clinical trial. Look for opportunities to expand and deepen clinical trial process expertise across functional teams, regions, and external partners and make decisions on process and issues affecting study implementation and execution.
  • Be knowledgeable on the global and regional operating model; coordinate and facilitate obtaining regional input to provide to the study teams.
  • Project Management, and Regional Operational Knowledge

DUTIES:

  • Broader responsibilities at Therapeutic Area/ Molecule/Indication level (e.g. attending relative critical chain network builds, providing input on strategy).
  • Use project management skills, processes, and tools to develop and execute local, regional, and/or global clinical trials (CT) as described:
  • Scope - Understand the scope of work required to complete the clinical trial successfully. Monitor the status and make adjustments and changes (per change control process) as needed to meet the deliverables of the trial.
  • Timeline – Develop and track global trial enrollment plan by gaining alignment and integrating inputs across functions and geographies.