Clinical Research Coordinator (Munster, IN)

Profound Research LLC; Munster (IN); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Health insurance

PTO

Retirement plan

Professional development

Job summary

Profound Research LLC in Munster, IN is seeking a Clinical Research Coordinator to manage all trial activities under supervision, ensuring compliance with protocol, laws, and company values.

You will coordinate study start-up, vendor management, subject recruitment, data collection, and adverse event reporting, while mentoring staff and maintaining rigorous documentation practices across sites.

Qualifications

• Bachelor’s degree and 2 years relevant life science experience OR
• Associate’s degree with 4 years relevant life science experience OR
• High School/Technical degree with minimum 6 years relevant life science experience and 1 year Clinical Research Coordinator experience

Responsibilities

• Conduct and manage all clinical trial activities per protocols and regulatory requirements.
• Complete required training including ICH-GCP and IATA certifications.
• Mentor and train staff in trial conduct and management.
• Lead study start-up, vendor management, subject recruitment, data collection, and adverse event reporting.
• Ensure good documentation practices across source documents, CRFs, and regulatory forms.
• Communicate effectively with coworkers, leadership, sponsors, CROs, and vendors.
• Collect and account for supplies from sponsors.
• Other duties as assigned.

Skills

Attention to detail

Communication

Independent work

Team player

Education

Bachelor’s degree + 2 years life science

Associate’s degree + 4 years life science

High School/Technical +6 years life science +1 CRC experience

Job description

About Profound Research

Profound Research partners with community physicians to offer clinical trials as a therapeuticoptionfor their patients. We handle all infrastructure, regulatory compliance, and administrative operations so physicians can focus on patient care. Our model gives patients access to the newest therapies whilemaintainingthe trusted patient-physician relationship.

Our Mission: Improving Lives by Providing Advanced Therapeutic Options

Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research

Our Values:

• Compassion: We prioritizethe patient-physicianrelationship, ensuring every interaction is service-oriented and patient-centered.
• Urgency: We work hard and practice selflessness, acting swiftly and decisively to meet the needs of our patients, partners, and colleagues.
• Solution Orientation: We embrace challenges with a positive mindset, communicate directly, andidentifyand implement effective solutions with efficiency.
• Excellence: We insist on excellence, holding ourselves accountable and empowering each other to deliver best-in-class service while maintaining the highest ethical and scientific standards.

Role: Clinical Research Coordinator

Company: Profound Research

Location: Munster, IN

Why this Role Exists

The Clinical Research Coordinator will manage all clinical trial activities under supervision in compliance with all applicable laws, regulations, and procedures of study protocol while maintaining company mission, vision and values.

Responsibilities

• Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements.
• Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner.
• Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills.
• Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
• Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.
• Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors.
• Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products.
• Other duties as assigned.

Requirements

• Bachelor’s degree and 2 years relevant experience in the life science industry OR
• Associate’s degree with 4 years relevant experience in the life science industry OR
• High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
• Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
• Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
• Proficient ability to work independently, plan and prioritize with minimal guidance
• Excellent attention to detail, organization, and communication with varied stakeholders
• Ability to work as a team player with the ability to adapt to changing schedules and assignments

Travel Requirements

Daily commute to site(s)

Physical Requirements & Work Environment

• This role is performedon-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
• Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
• Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
• May be required to wear personal protective equipment (PPE) in accordance with facility protocols
• Travel between company sites, meetings, or partner locations may be required
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role

Why Join Profound Research?

• Meaningful Impact: Every role at Profound contributes to advancing medical knowledge and expanding therapeutic options for patients – the work we do here matters
• Professional Growth: We invest in our people through comprehensive training, certification support, and ongoing education to help you grow in your role and your career
• Leadership & Advancement: Profound is a place where initiative is recognized. We actively support internal growth and create pathways for people to take on greater responsibility over time
• Collaborative Culture: You’llwork alongside a team of dedicated professionals who are passionate about clinical research and committed to doing it well
• Full Benefits Package: Competitive compensation, health insurance, PTO, retirement plan, and professional development support
• Diverse Clinical Exposure: Work across multiple therapeutic areas and study phases, building a breadth of experience that’s rare in a single organization