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Internship Real World Evidence Rwe Jobs in Austin, TX

Head of Clinical & Registry Programs

Austin, TX · On-site +1

$79K - $108K/yr

We're building the clinical operations and real-world evidence function that turns that network ... Skills, Knowledge and Expertise Required * 8+ years in RWE and/or registry programs and/or phase 4 ...

Marketing Intern

Austin, TX · On-site

$14.75 - $19.75/hr

Laptop provided for the duration of the internship * Real-world experience building brand strategy at a growing national company * A collaborative, supportive team that goes the extra mile Academic ...

Marketing Intern

Austin, TX

$14.75 - $19.75/hr

Laptop provided for the duration of the internship * Real-world experience building brand strategy at a growing national company * A collaborative, supportive team that goes the extra mile Academic ...

Future Internship Opportunities

Round Rock, TX · On-site

$14 - $18.75/hr

Interns at Ametrine benefit from a supportive environment, real-world experience, and the chance to be part of a mission that matters. Please submit your resume and a brief cover letter that outlines ...

RWE Americas, LLC To start as soon as possible, full time, permanent Functional area: Business ... Comfortable managing to contractual deadlines where missed milestones carry real commercial ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

Development Internship

Austin, TX · On-site

$15.50 - $20.75/hr

Interns will work with our development team to gain hands-on experience in donor stewardship ... Strengthen your resume with real-world experience, measurable accomplishments, and professional ...

New

Development Internship

Austin, TX · Hybrid

$15.50 - $20.75/hr

Interns will work with our development team to gain hands-on experience in donor stewardship ... Strengthen your resume with real-world experience, measurable accomplishments, and professional ...

New

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

We give interns real-world experience, helping them grow through hands-on projects, mentorship, and collaboration. Their fresh ideas and perspectives challenge us to think differently, and in return ...

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Internship Real World Evidence Rwe information

See Austin, TX salary details

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How much do internship real world evidence rwe jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for internship real world evidence rwe in Austin, TX is $15.41, according to ZipRecruiter salary data. Most workers in this role earn between $12.40 and $17.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Internship Real World Evidence (RWE) professional, and why are they important?

To thrive as an Internship Real World Evidence (RWE) professional, you need a solid background in life sciences, epidemiology, or statistics, often supported by progress toward a relevant degree. Familiarity with data analysis tools like SAS, R, or Python, and experience with healthcare databases or real-world data systems, are typically required. Strong analytical thinking, attention to detail, and collaborative communication skills help interns excel in cross-functional teams and data-driven projects. These competencies are crucial for generating robust, actionable insights from real-world data to inform healthcare decisions and policy.

What is an Internship in Real World Evidence (RWE)?

An Internship in Real World Evidence (RWE) offers students or recent graduates hands-on experience in collecting and analyzing data from real-world sources, such as electronic health records, insurance claims, and patient registries. RWE is used in the pharmaceutical and healthcare industries to evaluate the effectiveness, safety, and value of medical treatments outside controlled clinical trials. Interns may support research studies, help interpret data, and contribute to reports that inform decision-making for healthcare providers and regulators. This type of internship is ideal for those interested in data analysis, public health, and evidence-based medicine.

What types of projects do interns typically work on in a Real World Evidence (RWE) internship?

As an RWE intern, you can expect to contribute to projects involving the collection, analysis, and interpretation of real-world healthcare data, such as electronic health records, claims data, or patient registries. Common responsibilities include supporting data cleaning, conducting literature reviews, assisting with statistical analyses, and preparing reports or presentations for internal teams. You will often collaborate with cross-functional teams including epidemiologists, data scientists, and medical affairs professionals, which provides excellent exposure to various aspects of the pharmaceutical or healthcare industry.

What is the difference between Internship Real World Evidence Rwe vs Data Analyst?

AspectInternship Real World Evidence RweData Analyst
Required CredentialsTypically pursuing or recent graduate in healthcare, life sciences, or related fieldsBachelor's degree in statistics, mathematics, computer science, or related fields
Work EnvironmentHealthcare or pharmaceutical companies, research organizations, or academic institutionsVarious industries including finance, healthcare, marketing, and technology
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare sectors for evidence generationWidely used across multiple industries for data analysis and reporting

While both roles involve working with data, an Internship Real World Evidence Rwe focuses on analyzing real-world healthcare data to generate evidence for medical decisions, often within healthcare or pharma settings. A Data Analyst has a broader scope, working with various data types across industries to interpret and visualize data for business insights.

What cities near Austin, TX are hiring for Internship Real World Evidence Rwe jobs? Cities near Austin, TX with the most Internship Real World Evidence Rwe job openings:
Infographic showing various Internship Real World Evidence Rwe job openings in Austin, TX as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $32,048 per year, or $15.4 per hour.
Head of Clinical & Registry Programs

Head of Clinical & Registry Programs

Join Parachute

Austin, TX • On-site, Remote

$79K - $108K/yr

Full-time

Posted 10 days ago


Join Parachute rating

6.4

Company rating: 6.4 out of 10

Based on 9 frontline employees who took The Breakroom Quiz


Job description

Head of Clinical & Registry Programs
Department: Specialty Programs
Employment Type: Full Time
Location: Austin, TX
Description
Join Parachute operates a national, software-enabled biologics platform with 55 plasma and blood collection centers across 20 states, serving over 500k donors. That footprint is the foundation for a longitudinally-engaged donor population that can power the next generation of blood-based clinical research.
We're building the clinical operations and real-world evidence function that turns that network into a recruitment and biospecimen engine. This starts with observational studies and registries in high-growth, blood-based diagnostic areas such as multi-cancer early detection (MCED) and blood-based Alzheimer's and neurodegenerative testing, and scaling toward interventional research over time. You'll build that capability from the ground up.
We're hiring our first Head of Clinical & Registry Programs to design, launch, and advise on building a multi-site observational registry . This is an in-house, sponsor-side role: you will be the program, not manage a CRO that runs it for you.
You will own the registry from blank page to enrollment: registry design and protocol authoring, central IRB strategy (Advarra/WCG), and internal cross-functional partnership to bring it to life. This is fundamentally about standing up the infrastructure to systematically collect and govern observational data - not running an interventional experiment.
Key Responsibilities
  • Lead end-to-end registry design and author the registry protocol, charter, informed consent / authorization language, regulatory packets, data dictionary, etc. in partnership with the medical director and steering committee.
  • Lead consent and privacy strategy: full consent vs. HIPAA waiver vs. limited data set + DUA. Defend the choice to the IRB and to internal legal/privacy.
  • Select and engage the central IRB (Advarra or WCG); negotiate the Master Services Agreement and reliance framework.
  • Build and execute the site-activation playbook: feasibility, qualification, site participation agreements, BAAs/DUAs, regulatory packets, training.
  • Select and configure the EDC/registry platform (REDCap, Castor, Medidata RWS, or equivalent); spec CRFs, edit checks, and query workflows.
  • Stand up the eTMF (Veeva Vault, Florence, or structured equivalent) to DIA TMF Reference Model standards.
  • Get to First Subject In within 6-9 months of start.

Skills, Knowledge and Expertise
Required
  • 8+ years in RWE and/or registry programs and/or phase 4 experience
  • Has designed and built at least one registry from the ground up - registry design, protocol authoring, and the regulatory/start-up documentation to set it up - whether in an industry/sponsor-side or academic/research setting. Led at least one multi-site observational registry or post-marketing study from protocol through enrollment or has deep experience in phase 4 trials
  • Comfortable operating in a data-collection paradigm (observational registries) as distinct from running an interventional experiment - you understand the design, governance, and quality demands specific to systematically collecting longitudinal real-world data.
  • Working command of ICH E6(R3) GCP, 45 CFR 46 (Common Rule), HIPAA Privacy/Security, and 21 CFR Part 11.
  • Has authored or successfully defended an IRB waiver of consent / waiver of HIPAA authorization.
  • Direct working experience with Advarra and/or WCG as central IRB.
  • Hands-on with at least one EDC/registry platform (REDCap, Castor, Medidata Rave RWS, OpenClinica, Veeva CDMS).
  • Has built and negotiated site participation agreements and BAAs/DUAs at scale (10+ sites).
  • Has been through at least one FDA BIMO inspection or rigorous sponsor audit.
  • Has significant and direct experience interacting with FDA CBER

Strongly Preferred
  • Academic or research-institution registry experience (e.g., investigator-initiated or epidemiologic registries), in addition to or alongside industry experience.
  • Blood, transfusion medicine, hematology, or apheresis exposure.
  • Working knowledge of AABB standards, donor eligibility (21 CFR 630), and blood establishment regulations.
  • Experience interacting with FDA, and CBER in particular.
  • Start-up or small-company operating experience.
  • Familiarity with state privacy law overlays (CCPA/CPRA, WA MHMD, TX HB 300).

Nice to Have
  • CCRP, CCRA, RAC, or CIP certification.
  • Experience with payer/HEOR-driven registries.
  • Exposure to eConsent platforms (DocuSign Life Sciences, Medidata Patient Cloud, Castor eConsent).

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