---
title: 'Manager, Quality Control & Data Entry at Celerion'
canonical: 'https://feeny.ai/job/manager-quality-control-data-entry-celerion-tempe-m7k3wt0r5ngc'
type: 'job'
last_seen: '2026-09-07'
---

# Manager, Quality Control & Data Entry at Celerion

- **Company:** Celerion
- **Location:** Tempe, AZ
- **Employment:** full-time
- **Work type:** onsite
- **Posted:** 2026-09-01
- **Last confirmed live:** 2026-09-07
- **Apply:** https://jobs.lever.co/celerion/e34524f0-0abb-44b7-9e3a-b7e5350c9098

## Job description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

Responsible for managing the data workflow through Quality Control (QC) and Data Entry (DE) for studies, maintains timelines for client deliverables and ensures regulatory compliance.  Requires interface with other departments and/or sites.  Requires interface with Sponsors.

Essential Functions

- Responsible for staff management in accordance with the organization's policies and applicable laws
- Responsibilities include interviewing, hiring, and training employees; planning, assigning and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; development and coaching of employees
- Communicate and provide support/guidance to appropriate groups/staff as required to ensure established, revised and/or new processes are followed to ensure quality on-time/zero defect standards
- Plan, organize and facilitate workloads and schedules of staff to ensure that timelines are met and are compliant with regulatory and internal procedure requirements.
- Attend and participate in study specific meetings related to study set up, timeline production and management, and study status
- May be required to carry out study tasks, including but not limited to, complete QC review of source data and raw data for studies, performing accurate data entry, attending internal study initiation meetings to determine QC criteria and timelines for studies
- Write QC and DE SOPs and Procedure guides and participate in SOP and Procedure Guide Reviews
- Create and track metrics associated with QC and DE responsibilities
- Present the QC processes to sponsors and auditors
- Lead Process Improvement initiatives to improve the quality of the source data
- Participate in regulatory inspections, audits and meet with Sponsors as required
- Monitor process efficiency and implement process improvement as needed, including data flow and identification of error trends and resolutions.
- Lead and/or participate in problem solving for the data collection, quality control and data entry processes.

Knowledge/Skills/Education/Licenses

- Bachelor’s degree in a related field is required.
- 1-2 years of supervisory or trainer/leader experience required.
- Knowledge of Good Clinical Data Management Practices, Medical Terminology, GCP, ICH Guidelines, and 21 CFR Part11 preferred
- Ability to adjust hours to meet workload priorities
- Strong process improvement skills and change management experience
- Critical thinking skills
- Clinical data experience preferred
- **Equivalent education and experience will be consider

Celerion Values:       Integrity   Trust   Teamwork   Respect

Are you ready to join our team?

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

## About Celerion

## Company Overview
- **One-liner**: Celerion is a global contract research organization (CRO) specializing in early-phase clinical trials and bioanalytical services to accelerate drug development for pharmaceutical and biotechnology partners.
- **Entity Type**: Private (no public ticker; no funding rounds disclosed – operates as an established, privately-held CRO)
- **Headquarters**: Lincoln, Nebraska, USA
- **Founded**: 1969 (legacy company); current entity operates under the Celerion name with 50+ years of experience
- **Founders**: Not publicly available

## Core Business
- **Primary industry**: Clinical Research / Contract Research Organization (CRO) – early-phase drug development
- **Target customers**: Pharmaceutical and biotechnology companies (B2B)
- **Mission or purpose**: Accelerating the development of breakthrough therapies to address patient needs, enabling faster go/no-go decisions and speed-to-market for new treatments.

## Products & Services
- **Early Phase Services**: Fully integrated clinical trial management across Phase I/IIa studies, with dedicated inpatient clinics (650+ beds worldwide) and experienced medical/nursing staff.
- **Global Clinical Development**: Project-based support for complex studies across 30+ countries, from study award to database lock.
- **Bioanalytical Sciences**: PK, immunogenicity, and biomarker assays supporting all phases of drug development, with laboratories in Lincoln, NE and Zurich, Switzerland.
- **Drug Development & Regulatory Affairs**: Strategic guidance for clients initiating clinical studies, helping enable early and informed decisions.
- **Data Management & Biometrics**: Study design, modeling & simulation, biostatistics, clinical data management, and medical writing.

## Market Standing
- **Valuation/Market Cap**: Not disclosed (privately held)
- **Key Metric**: More than 1,000 full-time scientific and medical personnel; 650+ beds across clinics in North America, Europe, and Asia
- **Notable Investors/Partners**: Not publicly listed (operates as a standalone CRO)
- **Growth Signals**: 50+ years of industry experience; 80% of management roles filled through internal promotions; global presence in 30+ countries; continued expansion of facilities and service lines.

## Competitive Advantages
- **Largest global network of early-phase operations** – 650+ beds allow rapid patient recruitment and high-throughput studies.
- **Speed and reliability** – Company name derived from Latin “celeritas” (swiftness); built to deliver key data faster for earlier decision-making.
- **Integrated bioanalytical + clinical services** under one roof reduces handoff delays and maintains data consistency.
- **Deep expertise** – 50+ years of early-phase experience with a proven track record of regulatory submissions.

## Strategic Focus
- Continuing to expand global clinic and laboratory footprint to serve a broader set of clients and geographies.
- Investing in data science and modeling capabilities to answer complex client questions more quickly.
- Strengthening internal talent pipelines through leadership development and promotion-from-within programs.

## Why Work Here
- **Culture**: Emphasizes inclusion, collaboration, and employee well-being; “passion for helping people” is core to the mission.
- **Career growth**: 80% of management roles filled internally; Leadership Accelerator Program; specialized learning opportunities including industry conferences and scientific publications.
- **Work environment**: Some teams offer remote or hybrid work options; fast-paced, scientific atmosphere.
- **Benefits (U.S. employees)**: Medical, dental, prescription, vision; 401(k) with company match (after 1 year) and Student Debt Retirement Savings Match; HSA/FSA; tuition reimbursement; paid vacation, sick, and holiday leave; short/long-term disability; life insurance; voluntary plans (critical illness, accident, pet insurance, legal assistance).
- **Diversity & Inclusion**: Committed to creating an inclusive environment where all employees feel valued and can bring their authentic selves to work.

## Sources
1. [Celerion Careers Page](https://www.celerion.com/careers/)
2. [Celerion Homepage](https://www.celerion.com/)
3. [Celerion About Page](https://www.celerion.com/about/)
4. [Celerion Jobs on Lever](https://jobs.lever.co/celerion)
5. [Celerion Services Page](https://www.celerion.com/services/)

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