Internship Clinical Research -Talent Community Graduates ; Southern California)

Profound Research partners with community physicians to offer clinical trials as a therapeutic option for 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 while maintaining the trusted patient-physician relationship.

Improving Lives by Providing Advanced Therapeutic Options

Creating the Absolute Best Patient-Physician Experience in Clinical Research

• Compassion:
  We prioritize the patient-physician relationship, 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, and identify and 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.

While specific responsibilities will vary by site, study, and future opportunity, clinical research interns may have the opportunity to:

Future internship opportunities with Profound Research are paid. We are also willing to collaborate with your college or university to meet applicable internship or academic program requirements, including required hours, documentation, learning objectives, evaluations, and other school-specific requirements.

• Support clinical research studies and participant visits under appropriate supervision.
• Assist with participant flow, including greeting participants, rooming, and preparing for study visits.
• Support data collection and clinical research documentation.
• Assist with organizing study materials, supplies, and visit documentation.
• Gain hands-on exposure to clinical procedures such as vital signs, EKGs, phlebotomy, specimen collection, and specimen processing, as appropriate.
• Support laboratory and specimen-related workflows.
• Learn how clinical research protocols are implemented in a real-world research environment.
• Gain exposure to Good Clinical Practice (GCP), Good Documentation Practices, SOPs, and regulatory requirements.
• Interact with study participants and contribute to a positive, patient-centered experience.
• Work alongside Clinical Research Coordinators, investigators, and other research professionals.
• Become familiar with clinical research systems, documentation platforms, and study workflows.
• Learn how clinical trials contribute to the development of new therapies.

• This role is performed on 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

• 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…