715 matching jobs for “Senior Clinical Research Associate”

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Merck (MSD)

Digital and Data Quality (Snr Specialist)

IRL - Tipperary - Ballydine

… (Snr Specialist) to join the global Digital & Data Quality (DDQ) team in Ballydine, reporting to the Associate Director of DDQ for EMEA. In this hands-on role, you will support manufacturing, laboratory, and logistics …

Added Oct 16, 2026

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Abbott Laboratories

Instrumentation/Automation Service Engineer I - OS

United States > Madison : 650 Forward Dr

Pay posted by employer$22.45–$44.85 per hour

… of automation equipment. This encompasses automation across a range of laboratory settings, including clinical, research and development (R&D), manufacturing, and quality control laboratories. The automation used in …

Added Oct 15, 2026

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Labcorp Holdings

Intern-Animal Operations

Shanghai, China 3 postings

Full time
Internship

… Room and equipment compliance with GLP and AAALAC requirements. Learn how to identify, record, and review clinical observations, weight data, food consumption data, environmental data, and other data in appropriate data …

Added Oct 16, 2026

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Amgen

Legal Head, Mexico and Latam Distributors

Mexico - Mexico City

Full time
Regular

… cancer. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our …

Added Oct 15, 2026

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Becton Dickinson

Marketing Director, Strategic Customer Group

USA NJ - Franklin Lakes

In person
Full time
Regular

Pay posted by employer$192,000–$307,200 USD

… digital engagement, and field enablement. This is a rare role that combines the strategic altitude of a senior marketing leader with the executional ownership of a marcom director. Key Responsibilities Enterprise Brand …

Added Oct 27, 2026

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Danaher

Platform Information Security Officer (PISO), Life Sciences Platform

USA - Remote

Regular

Pay posted by employer$225,000–$275,000 per year

… operating companies serving the biopharma R&D, genomic medicine, and bioproduction ecosystem — Abcam (research antibodies and reagents), Aldevron (nucleic acid and protein CDMO for gene and cell therapies, gene …

Added Oct 15, 2026

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Abbott Laboratories

Instrumentation/Automation Service Engineer I

United States > Madison : 1 Exact Lane

Pay posted by employer$22.45–$44.85 per hour

Added Oct 22, 2026

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Abbott Laboratories

Instrumentation/Automation Service Engineer I - OS

United States > Madison : 650 Forward Dr

Pay posted by employer$22.45–$44.85 per hour

Added Oct 15, 2026

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Abbott Laboratories

Instrument/Automation Service Engineer I OS

United States > Madison : 650 Forward Dr

Pay posted by employer$22.45–$44.85 per hour

Added Oct 15, 2026

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Amgen

Biostatistical Programming Manager

United States - Remote

Added Oct 28, 2026

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Biogen

Director, US HCP Marketing - Lupus

Cambridge, Massachusetts, United States

Hybrid
Full time
Regular

Pay posted by employer$199,000–$274,000

… and patients to provide innovative solutions. The Director, US HCP Marketing – Lupus will be a senior leader on the US Lupus Marketing team, responsible for shaping and executing the HCP strategy as the …

Added Oct 16, 2026

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Merck (MSD)

Executive Director, PDMB Outsourcing

USA - Pennsylvania - West Point +3 locations

Pay posted by employer$255,800–$402,700

… leadership and talent management for the group through: Leading a team of ~35 professionals, including Senior Directors, PhD and BS/MS level scientists, including people management, scientific and operational …

Added Oct 16, 2026

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Humana (CenterWell)

Dispensing Pharmacist

West Chester Twp, OH

Full time
Regular

… Partner with fellow healthcare team members Ensure compliance with legal requirements within pharmacy Research medication issues, ensure accurate resolution, and provide guidance to team members and member clients when …

Added Oct 15, 2026

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Becton Dickinson

Field Service Engineer (Myrtle Beach or Florence)

USA SC - Moncks Corner +2 locations

Field
Full time
Regular

Pay posted by employer$28.20–$45.10 USD per hour

… our global reach, BD leads in patient and healthcare worker safety and the technologies that enable medical research and clinical laboratories. Our quality policy is straightforward….”We will consistently provide superior …

Added Oct 31, 2026

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Amgen

Process Analytical Engineer

Holly Springs, North Carolina, United States

Full time
Regular

… each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our …

Added Oct 15, 2026

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Merck (MSD)

Digital and Data Quality (Snr Specialist)

IRL - Tipperary - Ballydine

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Required Skills · employer excerpt

Current Employees apply HERE
Current Contingent Workers apply HERE
Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs /…

About this opportunity

Original employer description

Job Description

A wonderful opportunity has arisen for a Digital and Data Quality (Snr Specialist) to join the global Digital & Data Quality (DDQ) team in Ballydine, reporting to the Associate Director of DDQ for EMEA.

In this hands-on role, you will support manufacturing, laboratory, and logistics teams to assess, select, and validate computerized systems used in GMP processes, ensuring validation effort matches system complexity and risk. You will provide quality oversight for computerized systems used in support of GMP processes, provide expert Data Integrity (DI) guidance, and support inspection readiness.

At our company, we aspire to be the premier research-intensive pharmaceutical company. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We use the power of leading-edge science to save and improve lives around the world. As a Senior Specialist Digital and Data Quality, you will play a vital role in ensuring compliance with our company’s policies, procedures, and regulatory expectations.

Key Responsibilities

The responsibilities cover the quality aspects of data integrity, GMP computerized systems, master data management, laboratory instrumentation/systems, and supporting infrastructure used in site facilities, utilities, manufacturing, and laboratories to ensure compliance with company policies, procedures, and regulatory expectations.

•Act as a change driver and strategic lead to site processes within the global Quality Management System (QMS) framework.

•Influence the organizational future through review and approval of all quality-related activities, such as policies, procedures, plans, protocols, requirements, reports, deviations, and changes, as well as contributing to site inspection readiness.

•Introduce strategic initiatives on site, driving standardisation across the GMP environment for computerized systems and data integrity, and representing DDQ in global governance meetings for data integrity, computerized system validation, master data management, and lab instrumentation / systems.

•Promote cGMP and Data Integrity awareness and support a culture of continuous improvement. Help develop and maintain training on computerized systems validation, data integrity, and internal procedures.

•Work together with the business to resolve regulatory non-conformances for cGMP computerized systems and data integrity in a way that ensures business efficiency and compliance. Drive improvements on both a local and global level, based on emerging trends, compliance gaps, and system weaknesses.

•Act as a representative for DDQ management in site- and above-site meetings as needed.

Qualifications & Experience

•Bachelor’s degree, preferably in Science, Information Technology, Engineering, or equivalent.

•At least five years of demonstrable experience delivering validated IT solutions or working in an application support role.

•Strong understanding of the current pharmaceutical industry and applicable regulations (FDA/EU/ICH)

•Familiarity or practical experience in the implementation of quality systems in a pharmaceutical, laboratory, or manufacturing environment.

•Strong analytical and problem-solving skills, complemented by strong communication and teamwork skills that add great value to the team’s success.

•Timely decision-making and the ability to manage changing priorities, with strong project management skills, a sense of urgency, and a track record of delivering quality deliverables.

•Extended experience with deviations, CAPA, change control, master data, qualification/validation, and inspection readiness in a GxP environment.

Ballydine is the primary Drug Substance commercialisation hub within the network, where new processes are scaled and transitioned to commercial manufacture. The site supports clinical and commercial API supply and the transfer of processes and technologies across internal manufacturing sites and external partners.

We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of the world’s most challenging healthcare needs. So, if you are ready to: Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

Additional location(s) Compensation Information:

Required Skills:

cGMP Regulations, Change Management, Deviation Management, Good Automated Manufacturing Practice (GAMP), Manufacturing Quality Control, Pharmaceutical Quality Assurance, Product Disposition, Quality Auditing, Quality Management Standards, Regulatory Compliance, Risk Management, Strategic Planning

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

10/30/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

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