1

Internship Apple Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator

Dallas, TX · On-site

$24 - $32/hr

Fresh graduates with relevant internships or clinical research training are encouraged to apply. Key Responsibilities * Coordinate and manage clinical research studies in compliance with study ...

Clinical Research Coordinator 1

Pennington, NJ · On-site

$24.50 - $32.50/hr

One (1) year of experience in clinical research, healthcare, public health, community-based research, participant recruitment, or a related field which can include internships, academic research, or ...

next page

Showing results 1-20

Internship Apple Clinical Research information

See salary details

$2.1K

$6.4K

$7.8K

How much do internship apple clinical research jobs pay per month?

As of Aug 30, 2026, the average monthly pay for internship apple clinical research in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What is the difference between Internship Apple Clinical Research vs Clinical Research Coordinator?

AspectInternship Apple Clinical ResearchClinical Research Coordinator
Required CredentialsTypically pursuing or completed a relevant degree; no formal certification requiredOften requires a degree in health sciences or related field; certifications like CCR are common
Work EnvironmentInternship setting within Apple’s clinical research division, often in a corporate or tech-driven environmentClinical sites, hospitals, or research facilities managing trials
Employer & Industry UsageApple’s internal research projects, biotech collaborationsHospitals, research organizations, pharmaceutical companies

In summary, an Internship Apple Clinical Research is an entry-level position focused on supporting Apple’s clinical projects, often as a learning opportunity. A Clinical Research Coordinator is a more experienced role responsible for managing clinical trials, requiring specific certifications and experience. Both roles operate within the clinical research industry but differ in responsibilities and experience levels.

What cities are hiring for Internship Apple Clinical Research jobs?

Cities with the most Internship Apple Clinical Research job openings:

What are the most commonly searched types of Apple Clinical Research jobs?

The most popular types of Apple Clinical Research jobs are:

What states have the most Internship Apple Clinical Research jobs?

States with the most job openings for Internship Apple Clinical Research jobs include:

Clinical Research Coordinator

Winaxis

Dallas, TX • On-site

$24 - $32/hr

Full-time

Medical, PTO

Re-posted 15 days ago


Job description

Job Title : Clinical Research Coordinator (CRC)

Experience : 0–3 Years

Location : Dallas, Texas

Employment Type : Full-time

Job Summary:-

We are looking for a motivated and detail-oriented Clinical Research Coordinator to support the planning, execution, and management of clinical research studies. The ideal candidate should have 0–3 years of experience in clinical research and a strong understanding of Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements. Fresh graduates with relevant internships or clinical research training are encouraged to apply.

Key Responsibilities
  • Coordinate and manage clinical research studies in compliance with study protocols, ICH-GCP guidelines, and applicable regulations.

  • Screen, recruit, and enroll study participants.

  • Obtain informed consent from study participants.

  • Schedule and coordinate patient visits and follow-up appointments.

  • Collect, verify, and maintain accurate study documentation and source data.

  • Enter clinical data into Electronic Data Capture (EDC) systems.

  • Maintain Trial Master File (TMF), Investigator Site File (ISF), and essential study documents.

  • Report adverse events and serious adverse events according to protocol and regulatory requirements.

  • Coordinate with investigators, sponsors, CROs, and ethics committees.

  • Prepare for monitoring visits, audits, and regulatory inspections.

  • Ensure protocol compliance and participant safety throughout the study.

  • Assist with study start-up, close-out activities, and regulatory submissions.

Required Qualifications
  • Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, Microbiology, or a related field.

  • 0–3 years of experience in clinical research or clinical trial coordination.

  • Knowledge of ICH-GCP, FDA, and local regulatory guidelines.

  • Familiarity with EDC systems and Microsoft Office.

  • Strong organizational, communication, and documentation skills.

  • Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications
  • GCP Certification.

  • Clinical Research certification is an added advantage.

  • Experience with site coordination or patient recruitment.

  • Knowledge of clinical trial documentation and regulatory submissions.

Key Skills
  • Clinical Trial Coordination

  • ICH-GCP Compliance

  • Patient Recruitment

  • Informed Consent Process

  • Source Documentation

  • Electronic Data Capture (EDC)

  • Trial Master File (TMF)

  • Regulatory Documentation

  • Adverse Event Reporting

  • Data Management

  • Communication & Coordination

  • Attention to Detail

  • Time Management

Benefits
  • Competitive salary

  • Health insurance

  • Performance-based incentives

  • Training and career development opportunities

  • Paid leave and holidays

  • Exposure to global clinical research projects

How to Apply

Interested candidates can submit their updated resume along with a cover letter highlighting their clinical research experience, certifications, and relevant skills.