Remote Clinical Research Associate / Assistant Careers — Complete International Guide (Skills, Certifications, Career Paths, 100+ Hiring Sites & Live URLs)

Levi Cheptora

Sat, 25 Oct 2025

Quick orientation — why this guide

Remote and hybrid clinical trials (decentralized clinical trials) expanded dramatically after 2020 and now many CROs, pharma, tech-platforms and NGOs hire CRAs/Research Assistants for remote roles (monitoring, data review, site support, eCOA oversight, etc.). This guide gives the practical career map, certifications that matter, myths vs what actually works — and 100+ live links to companies, CROs, job boards and organisations actively recruiting for remote clinical research roles. For category-level sourcing on major CROs, decentralized-trial vendors and niche job boards, see industry lists and job hubs. proclinical.com+2Roots Analysis+2

What is a Remote Clinical Research Associate / Assistant?

• CRA (Remote): monitors clinical trial conduct and data remotely — source document review (when allowed), eCRF/data queries, vendor oversight, remote SDV (source data verification), risk-based monitoring, site training, regulatory document checks, escalation of safety or compliance issues.
• Clinical Research Assistant / Coordinator (Remote-friendly roles): supports study operations — scheduling remote visits, consenting support (eConsent platforms), data entry, query resolution, patient engagement & retention activities, coordination with sites and vendors.

Typical responsibilities (remote)

• Virtual site monitoring (telecon, eCRF checks, eSource review where permitted)
• Query management and data reconciliation
• Review of regulatory & ethics documentation (eTMF tasks)
• Patient-facing telehealth visits, eConsent and remote assessments (if clinically qualified)
• Liaison with vendors (lab, imaging, eCOA) and central monitoring teams
• Safety reporting support and escalation

Core skills & tools hiring managers look for

• Clinical research fundamentals: ICH-GCP familiarity, protocol adherence, clinical trial phases
• Technical skills: eCRFs (Medidata Rave, Oracle/EDC, Castor), CTMS (Veeva, Oracle), eTMF platforms, eConsent, ePRO/eCOA tools, MS Excel (pivot tables), remote monitoring tools (Zoom/Teams with secure processes)
• Soft skills: clear written English, cross-cultural communication, independence, time management, triaging escalation, attention to documentation and timelines
• Clinical background advantage: RN / PharmD / MD / BSc biomedical or life-sciences + site experience speeds hiring for remote CRA roles that require clinical judgement

Relevant certifications & licences (with authoritative links)

• Good Clinical Practice (GCP / ICH-GCP) — mandatory expectation for most roles; widely available via institutional courses and CITI Program. Grants.gov+1
• Example: NIH / CITI / institutional GCP courses.
• ACRP (Academy of Clinical Research Professionals) — CCRC, CCRA, ACRP-CP credentials for CRAs/CRCs. ACRP certs are well-recognised internationally. ACRP
• https://acrpnet.org/certification
• SOCRA (Society of Clinical Research Associates) — CCRP certification (internationally recognised). socra.org
• https://www.socra.org/certification
• Other useful certificates: Project Management (PMP or PRINCE2 basics for senior roles), data privacy (GDPR training), clinical data management modules (Medidata, Oracle training), site monitoring / remote monitoring training offered by many CROs.
• Professional licence: For roles requiring clinical assessments (tele-visits), an active nursing or medical licence in the relevant jurisdiction may be required.

Career path — typical ladder (remote-friendly progression)

1. Clinical Research Assistant / Data Coordinator (entry) — remote-friendly admin + data work
2. Clinical Research Coordinator (CRC) / Junior CRA — site-facing or remote CRC support
3. Clinical Research Associate (CRA) — remote monitoring, vendor oversight
4. Senior CRA / Lead CRA — project-level oversight, complex protocols
5. Clinical Trial Manager / Project Manager — budget, timeline, vendor mgmt
6. Clinical Operations Director / Head of Trials — strategy & portfolio
7. Lateral options: QA / Regulatory Affairs / Medical Writing / RWE / Clinical Data Science

Hacking your path: start with CRC/data roles, collect eCRF/EDC experience and GCP certification, then target remote CRA roles — some employers will take a candidate with strong eCRF/eTMF skills and site experience even without years of on-site monitoring.

Realistic salary snapshot (international / remote)

Salaries vary widely by country, employer and seniority. U.S. aggregates show CRAs commonly in the USD $70k–$140k range (median differs by source), Senior CRAs often exceed $120k; remote CRAs reported averages near $70–90k on some boards but top earners exceed $140k. Use local cost-of-living and employer benefits when evaluating offers. (Sources: Glassdoor, PayScale, Indeed). Glassdoor+2Payscale+2

Myths, facts & hiring hacks (what works / what doesn’t)

• Myth: “You must have a CRA certificate to get any CRA job.” → Fact: GCP + demonstrable eCRF/CTMS experience + site exposure often suffice for junior remote CRA roles. Certification helps career progression and pay. ACRP
• Myth: “Remote CRAs never travel.” → Fact: Many “remote” CRA roles are hybrid — occasional on-site visits for initiation or critical monitoring may be required. Clarify travel expectations in interviews.
• Hack (what works): Build a short portfolio of protocol review notes, monitoring checklists you’ve used, EDC screenshots (redacted) or a short project log showing query closure rates — recruiters love concrete evidence.
• Hack (networking): Join ACRP, SOCRA and LinkedIn clinical research groups; recruiters and hiring managers actively use these pools. LinkedIn
• What doesn’t work: Applying to hundreds of roles with a generic CV — target 5–10 tailored applications weekly with a focused cover note showing how your tools & GCP experience map to the job description.

Remote interview & CV tips (quick)

• CV: one page (entry)/two pages (senior). Add a short “Remote-ready” tech line: e.g., “Experienced with Medidata Rave, Oracle EDC, Veeva CTMS, eTMF; reliable remote setup (VPN, encrypted laptop) and HIPAA/GDPR awareness.”
• Interview: be ready with STAR examples: a time you closed complex queries, remediated a data discrepancy, or supported site activation remotely.
• Show timezone flexibility, strong written-communication samples (email or SOP excerpts), and willingness to travel if role requires.

100+ Actively Recruiting CROs / Pharma / Platforms / NGOs / Job Boards — categorized with working URLs

Note: this is a curated international list — many of these organisations post remote/hybrid CRA and clinical research support roles regularly. Use the careers/jobs links to search “remote” or “clinical research” directly on each site.

A. Global CROs & Contract Research Organisations (20)

1. IQVIA — https://www.iqvia.com/careers
2. ICON plc — https://www.iconplc.com/careers
3. Parexel — https://www.parexel.com/careers
4. PPD (Thermo Fisher / PPD) — https://www.ppd.com/careers (PPD is part of Thermo Fisher’s clinical business)
5. Syneos Health — https://www.syneoshealth.com/careers
6. Labcorp Drug Development (Covance / Labcorp) — https://www.labcorp.com/careers and https://www.labcorpdrugdevelopment.com
7. Charles River Laboratories — https://www.criver.com/careers
8. Medpace — https://www.medpace.com/careers
9. Fortrea — https://fortrea.com/careers
10. TFS HealthScience — https://www.tfshs.com/careers
11. Signant Health — https://www.signanthealth.com/careers
12. Novotech — https://www.novotech-cro.com/careers
13. PRA Health Sciences (note: PRA business largely integrated with ICON) — https://www.iconplc.com/careers (search PRA roles)
14. Clinipace — https://www.clinipace.com/careers
15. PAREXEL (repeat avoided) — (included above)
16. PSI CRO — https://www.psi-cro.com/careers
17. Worldwide Clinical Trials — https://www.worldwide.com/careers
18. InVitro International / Lab companies that support clinical trials (e.g., Labcorp already listed) — https://www.labcorp.com
19. Syreon? (regional CROs) — pick regional CRO pages when searching local markets (see ClinicalTrialsArena company A–Z). CCRPS Clinical Research Taininrg+1
20. Almac Group — https://www.almacgroup.com/careers

(Top CRO listings and marketplace changes referenced from industry directories.) proclinical.com+1

B. Big Pharma & Biotech — frequently hire remote CRAs or central monitors (20)

1. Pfizer — https://www.pfizer.com/careers
2. Johnson & Johnson (Janssen) — https://www.jnj.com/careers
3. Merck & Co / MSD — https://www.merck.com/careers
4. Novartis — https://www.novartis.com/careers
5. Roche — https://www.roche.com/careers.htm
6. AstraZeneca — https://careers.astrazeneca.com
7. Sanofi — https://www.sanofi.com/en/careers
8. GSK — https://www.gsk.com/en-gb/careers/
9. AbbVie — https://www.abbvie.com/careers.html
10. Eli Lilly — https://careers.lilly.com
11. Novo Nordisk — https://www.novonordisk.com/careers.html
12. Bristol Myers Squibb — https://careers.bms.com
13. Bayer — https://career.bayer.com/en/career
14. Amgen — https://careers.amgen.com
15. Moderna — https://www.modernatx.com/careers
16. Regeneron — https://www.regeneron.com/careers
17. Takeda — https://www.takeda.com/careers
18. Vertex Pharmaceuticals — https://www.vrtx.com/careers
19. Gilead Sciences — https://www.gilead.com/careers
20. Biogen — https://www.biogen.com/en_us/careers.html

(Big pharma often posts dedicated clinical operations / monitoring / RWE / safety roles.) proclinical.com

C. Decentralized / Virtual Trial Platforms & Clinical-tech (10)

1. Science37 — https://science37.com/careers
2. Medable — https://www.medable.com/careers
3. TrialSpark — https://www.trialspark.com/careers
4. Curebase — https://www.curebase.com/careers
5. Castor EDC — https://www.castoredc.com/careers
6. Medidata (Dassault Systèmes) — https://www.medidata.com/en/careers
7. Veeva Systems — https://www.veeva.com/company/careers/
8. ObvioHealth — https://www.obviohealth.com/careers
9. Antidote (patient-matching and decentralized study tools) — https://www.antidote.me/careers
10. Deep 6 AI — https://www.deep6.ai/careers

(Industry lists show these vendors as leaders in decentralized trials.) Roots Analysis+1

D. International NGOs, Charities & Global Health Organisations (10)

1. World Health Organization (WHO) — https://www.who.int/careers
2. Médecins Sans Frontières / Doctors Without Borders (MSF) — https://www.msf.org/jobs and https://career.ocb.msf.org for career paths. Doctors Without Borders+1
3. PATH — https://path.org/careers
4. Bill & Melinda Gates Foundation — https://www.gatesfoundation.org/careers
5. UNICEF — https://www.unicef.org/about/employ
6. Clinton Health Access Initiative (CHAI) — https://www.clintonhealthaccess.org/careers
7. Wellcome Trust — https://wellcome.org/careers
8. Save the Children — https://www.savethechildren.net/careers
9. USAID (global health programs) — https://www.usaid.gov/careers
10. UNAIDS / UN Careers — https://careers.un.org

E. Academic Medical Centres & Research Institutes (10)

1. Johns Hopkins Medicine — https://www.hopkinsmedicine.org/careers
2. National Institutes of Health (NIH) — https://www.nih.gov/about-nih/what-we-do/nih-role (jobs & trainees)
3. University of Oxford (Clinical Trials Unit & careers) — https://www.ox.ac.uk/about/jobs
4. Imperial College London — https://www.imperial.ac.uk/jobs
5. KEMRI (Kenya Medical Research Institute) — https://www.kemri.org/careers
6. MRC (UK Medical Research Council) — https://mrc.ukri.org/careers/
7. Aga Khan University (research & clinical roles) — https://www.aku.edu/careers
8. University of Cape Town — https://www.jobs.uct.ac.za/
9. Harvard Medical School / affiliated hospitals — https://hms.harvard.edu/about-hms/careers
10. ClinicalTrials.gov (resource for trials — not hiring portal but excellent for research needs): https://clinicaltrials.gov

F. Government / Regulatory & Public Health Agencies (10)

1. U.S. Food & Drug Administration (FDA) — https://www.fda.gov/about-fda/jobs-and-training-fda
2. European Medicines Agency (EMA) — https://www.ema.europa.eu/en/about-us/jobs
3. UK MHRA / UKHSA — https://www.gov.uk/government/organisations/medicines-and-healthcare-products-regulatory-agency/about/recruitment and https://www.gov.uk/government/organisations/uk-health-security-agency
4. Centers for Disease Control & Prevention (CDC) — https://www.cdc.gov/jobs
5. National Public Health Institutes (e.g., Africa CDC) — https://africacdc.org/careers
6. NIH jobs & fellowships — https://www.nih.gov/about-nih/what-we-do/nih-role
7. NHS careers (UK) — https://www.healthcareers.nhs.uk
8. Kenya Ministry of Health (careers & consultants may post) — https://www.health.go.ke/ (check country portals for national hiring)
9. Nigeria Centre for Disease Control (NCDC) — https://ncdc.gov.ng
10. European & national public health jobs: check local health ministries and government portals (varies by country)

G. Pharma / Life-sciences Job boards & Niche Recruiters (20+)

1. LinkedIn Jobs — https://www.linkedin.com/jobs (search “remote clinical research”) LinkedIn
2. Indeed — https://www.indeed.com
3. Glassdoor — https://www.glassdoor.com
4. BioSpace Jobs — https://jobs.biospace.com/jobs/clinical-research/ jobs.biospace.com
5. CenterWatch Jobs — https://www.centerwatch.com/careers/jobs/clinical-research-jobs/
6. PharmaOpportunities — https://pharmaopportunities.com
7. PharmiWeb.jobs — https://www.pharmiweb.jobs
8. Nature / Nature Careers — https://www.nature.com/naturecareers
9. Monster — https://www.monster.com
10. FlexJobs (paid remote jobs board) — https://www.flexjobs.com
11. Remote.co — https://remote.co/remote-jobs/clinical/
12. We Work Remotely — https://weworkremotely.com
13. Remote OK — https://remoteok.com
14. Wellfound / AngelList — https://wellfound.com (startups & decentralized trial platforms)
15. JobsInClinicalResearch — https://jobsinclinicalresearch.com
16. MedZilla — https://www.medzilla.com
17. PharmiWeb (company news + jobs) — https://www.pharmiweb.com/jobs
18. ProClinical (recruiting & job board) — https://www.proclinical.com/jobs
19. Hays Life Sciences — https://www.hays.com/jobs/life-sciences
20. Randstad Life Sciences — https://www.randstadusa.com/jobs/life-sciences/
21. ClinicalTrialsArena company directory (A–Z) — https://www.clinicaltrialsarena.com/company-a-z/ Clinical Trials Arena

(Use job boards to set job alerts for “remote clinical research” / “remote CRA”.)

H. Staffing & Specialist Recruiters (10)

1. Kelly Scientific / Kelly Services — https://www.kellyservices.com/us/careers/
2. Aerotek Life Sciences — https://www.aerotek.com/en/careers
3. Hays Life Sciences — https://www.hays.com/careers
4. ProClinical (specialist recruiter) — https://www.proclinical.com
5. Real Staffing (life sciences staffing) — https://www.realstaffing.com (region dependent)
6. Barrington James — https://www.barringtonjames.com/careers
7. SRG (specialist life sciences recruitment) — https://srgtalent.com
8. NonStop Clinical (recruitment) — https://www.nonstoprecruitment.com/clinical
9. Cpl Healthcare — https://www.cpllifesciences.com
10. Michael Page Life Sciences — https://www.michaelpage.com/jobs/clinical-research

(Specialist recruiters often have exclusive CRA roles — create recruiter profiles.) Jake Jorgovan

How to use this list (practical playbook)

1. Set job alerts on LinkedIn, Indeed, BioSpace, CenterWatch for keywords: “remote CRA”, “remote clinical research”, “decentralized trials”, “central monitor”. LinkedIn+1
2. Apply selectively: tailor your CV (EDC, CTMS, GCP) to the JD — use 3 achievement bullets that map to the job.
3. Network: reach out to current CRAs on LinkedIn, join ACRP/SOCRA local groups, attend (virtual) conferences.
4. Leverage platforms: sign up on decentralized trial vendor sites (Science37, Medable) and startup hubs (Wellfound) — many hire remotely. Roots Analysis+1

Sample resume bullets for a Remote CRA

• “Performed remote central monitoring across 6 Phase II–III sites; reduced average query closure time from 11 to 4 days by coordinating daily query triage and liaising with site coordinators.”
• “Executed eTMF reconciliation and documented submission readiness for 3 clinical sites during pre-monitoring visits using Veeva; supported successful inspections.”
• “Administered eConsent workflows and trained site staff on ePRO platform, increasing patient retention by 18% over 6 months.”

Short list of trusted learning & certification links

• ACRP certification & resources — https://acrpnet.org/certification. ACRP
• SOCRA CCRP — https://www.socra.org/certification. socra.org
• NIH / CITI GCP training resources — https://grants.nih.gov/policy-and-compliance/policy-topics/clinical-trials/good-clinical-training and https://about.citiprogram.org/series/good-clinical-practice-gcp/. Grants.gov+1

Final quick checklist before you apply (remote CRA)

• Up-to-date GCP certificate (within 3 years)
• EDC / CTMS names on CV (Medidata, Oracle, Veeva, Castor etc.)
• One remote-specific line on CV: “Remote-work setup: encrypted laptop, stable 1 Gbps connection, VPN, time-zone flexibility”
• Be ready to demonstrate your clinical judgement with 2 concise STAR stories in interviews
• If internationally mobile, know whether the role requires work-authorization in the employer’s country (many require it)

Entry / Junior Remote Clinical Research Associate (CRA) — CV (Template)

John/Jane Doe
Email: jane.doe@email.com · Phone: +44 7X XXX XXXX · LinkedIn: linkedin.com/in/janedoe · Location: Nairobi, Kenya (remote; GMT+3)
Remote-ready: Encrypted laptop, VPN, reliable fibre (100 Mbps), flexible hours (UTC±4) · Eligible to work remotely for employers worldwide / Willing to travel ≤10%

Professional Summary

Organised and detail-oriented Clinical Research Assistant with 2 years’ experience supporting Phase II/III trials, eCRF data entry and regulatory documentation. Strong working knowledge of ICH-GCP, eTMF and Oracle/Medidata EDC. Proven ability to resolve data queries quickly, support remote monitoring visits and coordinate cross-functional vendor activity. Seeking a remote CRA role to apply central monitoring and CTMS skills.

Core Competencies

• Remote monitoring support · Risk-based monitoring (RBM) · Query resolution
• ICH-GCP compliance · eTMF & regulatory document control
• eCRF/EDC: Medidata Rave / Castor / Oracle (basic)
• CTMS: Veeva / basic CTMS workflows
• Patient-facing tele-visits / eConsent support
• Excellent written English · Cross-cultural communication

Technical Skills

Medidata Rave, Castor EDC, Oracle Clinical, Veeva CTMS, Microsoft Excel (pivot tables), MS Teams/Zoom, eTMF platforms, eConsent/ePRO basics

Professional Experience

Clinical Research Assistant (Remote Support) — HealthTrials Africa / Remote
Jan 2023 — Present

• Supported central monitoring for a Phase II vaccine study across 8 sites; triaged and closed 85% of data queries within 5 working days using Medidata.
• Performed eTMF reconciliations for site files and reduced outstanding TMF items by 40% before site initiation.
• Coordinated remote site activation tasks (document collection, eConsent setup) and prepared monitoring packs for virtual initiation meetings.
• Assisted in SAE documentation collection and prepared initial safety summaries for the safety team.

Clinical Data Intern — University Clinical Trials Unit, Nairobi
Jun 2021 — Dec 2022

• Entered and validated 1,200+ CRF records into Castor EDC; resolved discrepancies in collaboration with site CRCs.
• Maintained trial trackers and supported ethics submission document preparation.

Education

BSc. Biological Sciences — University of Nairobi — 2020

Certifications

• ICH-GCP Certificate — CITI Program — 2024
• Introduction to Clinical Data Management — Coursera — 2022

Additional

Languages: English (fluent), Swahili (native)
References: Available on request

Experienced Remote Clinical Research Associate — CV (Template)

Alex Sample
Email: alex.sample@email.com · Phone: +1 (555) 555-5555 · LinkedIn: linkedin.com/in/alexsample · Location: Remote (EST / willing to work UTC±5)
Remote-ready: Full encrypted remote workstation, company-grade VPN, HIPAA/GDPR aware; willing to travel up to 25% globally

Professional Summary

Proactive Senior Clinical Research Associate with 6+ years’ experience in monitoring Phase II–IV trials and leading remote central monitoring programs for oncology and infectious disease studies. Track record of improving query closure rates, executing risk-based monitoring plans, supporting TMF readiness for inspections, and training site staff on eConsent and ePRO platforms. Experienced with Medidata Rave, Oracle, Veeva CTMS and eTMF systems.

Key Skills

• Remote & hybrid monitoring · Vendor oversight · RBM & central monitoring
• eTMF readiness & inspection support · SAE/ISR reporting workflows
• Protocol compliance & corrective action plans
• Cross-functional leadership · Mentoring junior CRAs
• CTMS & EDC expert (Veeva, Medidata, Oracle)
• Stakeholder communication across time zones

Technical Proficiency

Medidata Rave, Oracle InForm, Veeva CTMS, eTMF (DigiTracking / Veeva Vault), Castor, eConsent (Medable), Microsoft Excel (advanced), PowerBI basics, Jira/Confluence, Zoom/WebEx

Professional Experience

Senior Remote CRA — Oncology (Lead CRA, Central Monitoring) — ICON plc (Contract)
Mar 2021 — Present

• Led central monitoring for a global Phase III oncology immunotherapy trial across 60+ sites; implemented centralized query algorithms that reduced data discrepancy rates by 28% in the first 6 months.
• Conducted remote source document review where permitted and coordinated focused on-site visits for high-risk sites, decreasing protocol deviation incidence by 22%.
• Mentored and trained a team of 5 junior CRAs on RBM tools and eTMF best practices; instituted a weekly metrics dashboard to track query closure SLAs.
• Managed vendor oversight for central labs and ePRO vendors; negotiated SLA changes and improved turnaround times for lab data integration.

Clinical Research Associate — Infectious Disease Studies — Medpace
Jan 2019 — Feb 2021

• Monitored Phase II/III trials across APAC and EMEA regions (remote + on-site visits); achieved 95% audit readiness in eTMF audits.
• Prepared monitoring reports and supported regulatory inspections; authored SOP amendments for remote monitoring procedures.

Clinical Research Coordinator — City Hospital Research Unit
Jul 2016 — Dec 2018

• Coordinated patient visits, consent process and source documentation for multiple interventional trials; collaborated with CRO monitoring teams.

Education

MSc Clinical Research — University of London (distance) — 2018
BSc Nursing (Registered Nurse) — University of Cape Town — 2014

Certifications & Licences

• ICH-GCP (CITI) — 2024
• ACRP — CCRA (or ACRP-CP) — 2022
• Registered Nurse — South Africa Nursing Council (active)
• GDPR / Data Privacy Awareness — 2023

Achievements / Metrics (Quick)

• Reduced average query closure time from 11 days to 4 days (Phase III trial).
• Achieved <2% protocol deviations across 60 sites through targeted remote monitoring.

Additional

Languages: English (native), French (conversational)
References: Available on request

Two-Line Cover Notes (paste-ready / interchangeable)

Option A — Mid / Senior CRA (Remote)
I’m an experienced Senior CRA with 6+ years in remote central and hybrid monitoring (Medidata, Veeva, RBM) who reduced query closure times by 60% and improved eTMF inspection readiness across multi-region trials. I’m excited to bring my remote-monitoring setup, vendor oversight experience and timezone flexibility to [Company Name]’s clinical operations team.

Option B — Entry / Junior CRA (Remote)
As a Clinical Research Assistant with hands-on eCRF and eTMF experience and a current ICH-GCP certificate, I’ve supported multi-site Phase II work and closed 85% of queries within 5 working days. I’m eager to contribute to [Company Name] as a remote CRA and support efficient central-monitoring activities.

ATS & Recruiter Keywords to include (copy into top of CV or skills)

Remote CRA, Clinical Research Associate, Central Monitoring, Risk-Based Monitoring, ICH-GCP, eCRF, EDC (Medidata Rave, Oracle, Castor), CTMS (Veeva), eTMF, SAE reporting, protocol compliance, eConsent, ePRO, vendor oversight, clinical operations, monitoring reports, query resolution

Quick Customization Checklist — How to turn the template into your CV in <10 minutes

1. Replace name/contact + LinkedIn.
2. Pick the version (Entry or Experienced) and edit the professional summary to reflect your years and therapeutic area.
3. In Experience, replace 2–3 bullets with your real metrics (e.g., number of sites, query closure rate, number of CRFs, percent reduction, travel %). Use numbers where possible.
4. Add real EDC/CTMS software names you’ve used. Add GCP cert with date.
5. Save as PDF and plain-text copy for ATS systems. File name: FirstnameLast_CRA_Remote.pdf

Sources & further reading (selected)

• ProClinical — Top CROs to watch (industry CRO ranking & consolidation). proclinical.com
• RootsAnalysis — Leading decentralized clinical trials companies. Roots Analysis
• BioSpace — active clinical research job listings. jobs.biospace.com
• ACRP (certification info) — https://acrpnet.org. ACRP
• SOCRA (certification) — https://www.socra.org. socra.org
• NIH / GCP guidance — https://grants.nih.gov/.../good-clinical-training. Grants.gov
• Glassdoor / PayScale / Indeed (salary data). Glassdoor+2Payscale+2