Data Coordinator & QC Reviewer

Pharmaron Beijing Co. Ltd.; Exton (PA); Presencial; USD 65 000 - 70 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Comprehensive Medical, Dental & Vision

401(k) Retirement Plan with employer-m

Paid Time Off & Holidays

Health Savings Account (HSA)

Life Insurance & AD&D

Employee Assistance Program

Professional development

Resumo da oferta

Pharmaron Beijing Co. Ltd. in Germantown, MD seeks a detail-oriented Data Coordinator & QC Reviewer to support the review, organization, quality control, and delivery of scientific data generated in a regulated laboratory environment.

This role ensures data accuracy, regulatory compliance, and timely transfer of study results to pharmaceutical and biotech clients, collaborating with scientists, PMs, QA, and QC teams.

Qualificações

• Bachelor's degree in Life Science or related field.
• Minimum 2 years of experience in a regulated laboratory, CRO, pharmaceutical, or clinical research environment.
• Working knowledge of GLP, GCP, ICH guidelines, and 21 CFR Part 11.
• Strong attention to detail and organizational skills.
• Proficiency in Microsoft Office, particularly Excel.
• Ability to manage multiple projects and meet deadlines.

Responsabilidades

• Review, compile, and organize scientific documents and study data in compliance with GLP, GCP, and internal SOPs.
• Perform quality control reviews of laboratory data and supporting documentation.
• Prepare and coordinate data transfers according to sponsor specifications and timelines.
• Generate and manage transfer files including Excel, CSV, PDF, and ZIP formats.
• Collaborate with scientists, project managers, QA, and QC teams to ensure accurate and timely data delivery.
• Support audit responses, reconciliation activities, and continuous process improvement initiatives.
• Track project timelines and communicate data transfer status to stakeholders.

Conhecimentos

Attention to detail

Organizational skills

Multi-tasking / manage multiple work #

Formação académica

Bachelor's degree in Life Science or related field

Ferramentas

Excel

LIMS

eTMF

Descrição da oferta de emprego

Position

Data Coordinator & QC Reviewer

Salary Range:

$65,000- 70,000

Location:

Germantown, MD

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, 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 887 discovery projects , 1,100+ CMC programs , and 1,397 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 3,300 global customers. To learn more, visit www.pharmaron.com.

Pharmaron is seeking a detail-oriented Data Coordinator & QC Reviewer to support the review, organization, quality control, and delivery of scientific data generated in a regulated laboratory environment. This role plays a critical part in ensuring data accuracy, regulatory compliance, and timely delivery of study results to our pharmaceutical and biotechnology clients.

Key Responsibilities

• Review, compile, and organize scientific documents and study data in compliance with GLP, GCP, and internal SOPs.
• Perform quality control reviews of laboratory data and supporting documentation.
• Prepare and coordinate data transfers according to sponsor specifications and timelines.
• Generate and manage transfer files including Excel, CSV, PDF, and ZIP formats.
• Collaborate with scientists, project managers, QA, and QC teams to ensure accurate and timely data delivery.
• Support audit responses, reconciliation activities, and continuous process improvement initiatives.
• Track project timelines and communicate data transfer status to stakeholders.

What We\'re Looking For

• Bachelor\'s degree in a Life Science or related field.

• Minimum 2 years of experience in a regulated laboratory, CRO, pharmaceutical, or clinical research environment.
• Working knowledge of GLP, GCP, ICH guidelines, and 21 CFR Part 11.
• Strong attention to detail and organizational skills.
• Proficiency in Microsoft Office, particularly Excel.
• Ability to manage multiple projects and meet competing deadlines.

Preferred Qualifications

• Experience with laboratory data management, quality review, or scientific document control.
• Experience supporting sponsor data transfers and regulatory inspections.
• Familiarity with LIMS, eTMF, or other regulated data systems.

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 US, UK, China, and Singapore. 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.

Benefits:

• Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance, AD\&D, Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP), mental health resources, and wellness programs
• Family-friendly benefits, including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

As an Equal Employment Opportunity and Affiantive 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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