PRN Outpatient Services Coordinator I (Clinical Research)

Baltimore · On-site

About this role

Position: PRN Outpatient Services Coordinator

Location: Baltimore, MD

FLSA Status: Non-Exempt, PRN 

Hourly Rate: $18-$20 Per hour 

About Pharmaron

Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life. With over 23,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 21,000 global customers. To learn more, visit www.pharmaron.com.

Job Overview:

As the PRN Outpatient Services Coordinator, you are responsible for performing the initial informed consent process with potential study subjects, collecting study-specific data as part of the screening process, completing outpatient study visits, conducting check in procedures on admission subjects.

We are conveniently located on the University of Maryland BioPark campus and provide paid parking for all employees. 

Responsibilities:

  • Follow Good Clinical Practices (GCPs) and adhere to Pharmaron CPC Standard Operating Procedures (SOPs).
  • Collaborate with departments to prepare required documentation for study screenings.
  • Screen potential participants to ensure study understanding and verify eligibility against protocol criteria.
  • Administer initial informed consent and explain study details to potential participants.
  • Review medical history and assess eligibility based on inclusion and exclusion criteria.
  • Confirm demographic information and assist with protocol‑required screening tests.
  • Respond to participant questions and complete all required screening documentation.
  • Perform clinical procedures such as vital signs, height/weight measurements, and ECGs.
  • Log subject information and update participant records in ClinSpark.
  • Conduct follow‑up visits for study participants in outpatient settings and conduct admission procedures for all study participants.
  • Perform quality assurance reviews of collected study data to ensure accuracy, consistency, and compliance.

What We're Looking For:

  • Associate or Bachelor's degree, preferably in biological science, nursing or other allied health profession.
  • Experience working cross-functionally with Project Manager, Clinical Research Coordinator and Research Associates

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

How to Apply:

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

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Company at a glance

Pharmaron: Global Life Sciences Services Provider

Stock Code: 300759.SZ/3759.HK

Founded in 2004, Pharmaron is a premier life sciences service provider that offers a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products.

Pharmaron’s Comprehensive CRO & CDMO Services

  • Synthetic, Medicinal, and Analytical Chemistry Services
  • Biology Services (e.g., in vitro screening, structural biology, biomarkers)
  • DMPK Services (e.g., in vitro ADME, in vivo PK, PKPD, mass balance)
  • Pharmacology Services (e.g., in vivo pharmacology, animal disease models, immunotoxicity)
  • Drug Safety Assessment Services (e.g., toxicology, safety pharmacology, genetic toxicology)
  • Radiochemistry and Isotopically Labelled Metabolism Services (e.g., 14C/Carbon-14 radiosynthesis, 3H/tritium radiosynthesis, QWBA, mARG)
  • CMC Services (e.g., API manufacturing, process chemistry, formulation development)
  • Clinical Development Services (e.g., First-in-Human [FIH], ethnobridging, microdosing Phase 0, absolute bioavailability)

Commitment to Excellence and Innovation

With a proven track record of success, Pharmaron continually invests in its people, facilities, and technologies to meet evolving scientific and regulatory demands. The company prides itself on enabling scientific breakthroughs and supporting its partners in advancing human health.

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Learn More: Explore Pharmaron’s services to discover how to accelerate your R&D programs. www.pharmaron.com.

Keywords: CRO, CDMO, synthetic chemistry, medicinal chemistry, biology, radiochemistry, toxicology, First-in-Human, API manufacturing, PKPD, 14C radiosynthesis, discovery biologics, clinical development, small molecules, biologics, cell and gene therapy (CGT) products

Founded2004
Team Size10,001+ employees
WorkspaceOn-site
IndustryPharmaceutical Manufacturing
Location
Baltimore, Maryland, United States
LinkedInLinkedIn

Top Benefits

  • Paid Parking

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