Clinical Research Associate - PhD in Life Sciences

Medpace; Irving (TX); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Competitive travel bonus

401K matching

Home office furniture allowance

Flexible work hours

Annual merit increases

Job summary

A leading clinical research organization is seeking a Clinical Research Associate in Irving, TX. This role requires a PhD or a Bachelor's in a relevant field, offering a unique career opportunity in drug research and development. The candidate will conduct site visits, verify information, and ensure protocol compliance, traveling 60-70% of the time. Training is provided to enhance skills and career advancement is available. Competitive pay and numerous benefits are included.

Qualifications

• Ability to travel 60-70% to locations nationwide.
• Must maintain a valid driver's license.
• Minimum 1 year healthcare-related work experience preferred.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites.
• Verify adequate investigator qualifications, training, and resources.
• Communicate with medical site staff.

Skills

Detail-oriented

Time management

Strong communication skills

Proficient in Microsoft Office

Education

Bachelor’s degree in a health or science related field

PhD (preferred)

Job description

Medpace Clinical Research Associate – PhD required

Positions are office based in our Irving, TX.

We are hiring PhD candidates at Medpace! The Clinical Research Associate position offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a Life Science background who want to explore the research field, travel the US, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

MEDPACE CRA TRAINING PROGRAM (PACE®)

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE® Training Program, you will join other professionals achieving CRA excellence. PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA. PACE® will prepare you by developing your CRA skills through interactive discussions and hands on job‑related exercises and practicums. To supplement your in‑house and field‑based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

WHY BECOME A CRA

• Dynamic working environment, with varying responsibilities day‑to‑day
• Expansive experience in multiple therapeutic areas
• Work within a team of therapeutic and regulatory experts
• Defined CRA promotion and growth ladder with potential for mentoring and management advancements
• Competitive pay and many additional perks unmatched by other CROs

WE OFFER THE FOLLOWING

• Competitive travel bonus
• Equity/Stock Option program
• Training completion and retention bonus
• Annual merit increases
• 401K matching
• Opportunity to work from home
• Flexible work hours across days within a week
• Retain airline reward miles and hotel reward points
• Home office furniture allowance, laptop, mobile phone with hotspot for internet access anywhere
• In‑house travel agents, reimbursement for airline club, TSA pre‑check
• Opportunity for leadership positions – Lead CRA, CRA Manager, Clinical Trial Manager, Training and Development Manager, and many more
• CRA training program (PACE®)
• Ongoing therapeutic training by our in‑house physicians who are medical and regulatory experts
• In‑house administrative support for all levels of CRAs; and
• Opportunities to work with international team of CRAs

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
• Communication with the medical site staff including coordinators, clinical research physicians, and their site staff
• Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
• Verification that the investigator is enrolling only eligible subjects
• Regulatory document review
• Medical device and/or investigational product/drug accountability and inventory
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
• Assess the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
• Completion of monitoring reports and follow‑up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance

Qualifications

• Must have a minimum of a Bachelor’s degree in a health or science related field; PhD preferred
• Ability to travel 60‑70% to locations nationwide is required, or less if remote/virtual visits required
• Must maintain a valid driver’s license and the ability to drive to monitoring sites
• Minimum 1 year healthcare‑related work experience preferred
• Proficient knowledge of Microsoft® Office
• Strong communication and presentation skills; and
• Must be detail‑oriented and efficient in time management

Medpace Overview

Medpace is a full‑service clinical contract research organization (CRO). We provide Phase I‑IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti‑viral and anti‑infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Dallas Perks

• Dallas Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company‑sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with nonprofit organizations
• Structured career paths with opportunities for professional growth
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on‑site fitness center
• Free on‑site parking
• Outdoor seating and workspace

Awards

• Named a Top Workplace in 2024 by The Cincinnati Enquirer
• Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What To Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.