ZipRecruiter

Log In

1

Clinical Contracts Manager Jobs in Indiana (NOW HIRING)

Ortho Clinical Diagnostics

The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical ... Effectively manage sales pipeline from lead acquisition to contract signing by focusing and ...

Damar Services, Inc.

Clinical Psychologist

Indianapolis, IN · On-site

$84K - $116K/yr

They will also provide clinical oversight to contract psychologists and interns. They will also ... Comprehensive training in verbal intervention and physical management techniques * Medical, Dental ...

Damar Health Services

Clinical Psychologist

Indianapolis, IN · On-site

$84K - $116K/yr

They will also provide clinical oversight to contract psychologists and interns. They will also ... Comprehensive training in verbal intervention and physical management techniques * Medical, Dental ...

previous pagenext page

Showing results 21-40

All JobsClinical Contracts JobsClinical Contracts Manager JobsClinical Contracts Manager Jobs in Indiana

Clinical Contracts Manager information

What does a clinical contracts manager do?

A Clinical Contracts Manager is responsible for negotiating, drafting, and managing contracts related to clinical trials in the pharmaceutical, biotechnology, or medical device industries. They work closely with clinical research teams, legal departments, and external partners to ensure that agreements comply with regulations and company policies. Their duties include overseeing contract timelines, resolving contractual issues, and ensuring that all parties adhere to agreed-upon terms. This role is crucial for the smooth execution of clinical studies and the protection of the company's interests.

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

To thrive as a Clinical Contracts Manager, you need expertise in contract negotiation, knowledge of clinical research regulations, and a bachelor’s degree in a related field. Familiarity with contract management systems, clinical trial management software, and regulatory databases is typically required, along with certifications such as CCRA or similar. Strong interpersonal, organizational, and problem-solving skills distinguish top performers in this role. These capabilities are essential to ensure contracts are compliant, timely, and support the smooth execution of clinical trials.

What are some common challenges faced by clinical contracts managers during the negotiation process, and how can they be addressed?

Clinical Contracts Managers often encounter challenges such as aligning timelines between sponsors and research sites, managing complex regulatory requirements, and reconciling differing expectations around budget and contract terms. Successfully addressing these challenges usually involves proactive communication with all stakeholders, maintaining up-to-date knowledge of industry regulations, and employing strong negotiation skills to reach mutually beneficial agreements. Building collaborative relationships and having a detail-oriented approach also help ensure smoother contract execution and project progression.

What is the difference between Clinical Contracts Manager vs Clinical Research Associate?

AspectClinical Contracts ManagerClinical Research Associate
Primary RoleManages contract negotiations and compliance with vendors and partnersMonitors clinical trial sites to ensure protocol adherence
Required CredentialsBachelor's degree, experience in contracts or legal knowledgeBachelor's degree, life sciences background, clinical trial experience
Work EnvironmentOffice-based, collaboration with legal and procurement teamsSite visits, monitoring clinical trial progress
Industry UsagePharmaceutical, biotech, clinical research organizationsPharmaceutical, biotech, clinical research organizations

The Clinical Contracts Manager focuses on negotiating and managing clinical trial contracts, ensuring compliance and legal adherence. In contrast, the Clinical Research Associate primarily monitors clinical trial sites to ensure protocol compliance. Both roles are essential in clinical research but serve different functions within the industry.

What are popular job titles related to Clinical Contracts Manager jobs in Indiana?

For Clinical Contracts Manager jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Clinical Contracts Manager jobs in Indiana look for?

The top searched job categories for Clinical Contracts Manager jobs in Indiana are:

What cities in Indiana are hiring for Clinical Contracts Manager jobs?

Cities in Indiana with the most Clinical Contracts Manager job openings:

Clinical Contracts Manager jobs near you
Infographic showing various Clinical Contracts Manager job openings in Indiana as of August 2026, with employment types broken down into 85% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution.

Site Manager (Clinical Trials Facility)

Protouch Staffing

Merrillville, IN

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

Clinical Research Site Manager

(Lead CRC or Senior CRC with Management Experience)

Location: Merrillville, IN

Job Type: Full-Time

Schedule: Monday-Friday (5x8 shifts)

Salary Range: $95K to $110K + Profit Distribution


Position Summary

The Clinical Research Site Manager is responsible for overseeing the daily operations of the clinical research site, ensuring strict protocol compliance, high-quality patient care, and seamless coordination with sponsors and CROs. This role leads site staff, monitors study performance, and ensures adherence to regulatory and ethical standards.


Key Responsibilities

  • Oversee daily site operations and ensure compliance with GCP, FDA, and ICH guidelines

  • Supervise and support Clinical Research Coordinators (CRCs), nurses, and clinical staff

  • Serve as the primary point of contact for sponsors, CROs, and monitors

  • Oversee patient recruitment, informed consent, and retention strategies

  • Ensure accurate data entry and timely resolution of data queries

  • Manage study budgets, contracts, and allocation of site resources

  • Maintain regulatory documentation and audit readiness


Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)

  • 3-5 years of clinical research experience

  • 1-2 years of leadership or site management experience

  • Strong working knowledge of GCP, FDA, and ICH regulations

  • Excellent leadership, communication, and organizational skills


Benefits

  • Health, Dental, and Vision Insurance

  • Paid Time Off (PTO)

  • Retirement Plan

  • Profit Distribution

Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

View All Protouch Staffing Jobs