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Research Associate (Per Diem - Weekends)

0-2 years
$20.00 – $22.00 per hour
10 Nov. 13, 2025
Job Description
Job Type: Full Time Part Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Research Associate (Per Diem – Weekends)

Location: United States – Baltimore, Maryland
Job ID: R0000034825
Category: Clinical Trials


About the Role

Position: Entry-Level Research Associate (Per Diem)
Work Type: On-site (Baltimore, MD)

At Parexel’s Early Phase Clinical Unit, we play a critical role in developing innovative new medicines through early phase and first-in-human trials — the first step in testing novel treatments in humans.

As a Research Associate, you will be essential to ensuring the success of Phase I clinical trials. This entry-level role offers excellent growth potential within Parexel — ideal for those aspiring to become enrollment specialists, clinical research coordinators, or clinical managers.


Key Responsibilities

After completion of training, you will:

  • Understand and follow study protocols, performing required medical procedures.

  • Recruit study participants by calling databases, attending community events, and posting flyers in various local venues (schools, senior centers, supermarkets, etc.).

  • Maintain accurate participant tracking systems, appointment calendars, and related documentation.

  • Conduct screening and protocol-specific visits, assisting staff physicians in reviewing medications, adverse events, and test results.

  • Prepare and monitor study supplies and stock levels in the clinic/hospital.

  • Ensure participant safety and compliance with clinical operating guidelines.

  • Assist in monitor visits (e.g., room setup and support).

  • Maintain high-quality source documentation and case report forms (CRFs).

  • Comply with Quality Management (QM) and Clinical Research Coordinator (CRC) requirements, ensuring timely corrections when needed.


Qualifications

Education

  • Bachelor’s degree in Life Sciences or a related field preferred, or

  • High School Diploma/GED with relevant medical or clinical experience

Preferred Certification

  • CPT/Phlebotomy certification (highly preferred)


Experience & Skills

  • Proven customer service experience in a fast-paced environment

  • Experience working in a medical or clinical setting

  • Ability to stand and walk for prolonged periods

  • Strong communication and interpersonal skills

  • Attention to detail and commitment to compliance


Work Schedule

  • Training Period:

    • Duration: 4–6 weeks

    • Hours: 30–40 hours/week

    • Schedule: Monday–Friday, 6:50 AM – 3:20 PM

  • Post-Training Schedule:

    • Weekend shifts: Saturday and Sunday (12-hour shifts)

    • Bi-monthly training sessions: May be required based on training availability

  • Employment Type: Per Diem (not eligible for full-time benefits)


Compensation

  • Base Pay Range: $20.00 – $22.00 per hour

  • Eligible for shift differentials

  • Actual pay may vary based on education, training, experience, and location


Additional Benefits

  • Some roles may be eligible for:

    • Annual performance-based bonus plan

    • Salary review and incentive programs

    • Paid time off, 401(k) match, life and health insurance, and other benefits (based on eligibility)


Equal Employment Opportunity

Parexel is an equal opportunity employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.