Clinical Trials Operations jobs

Associate Principal Scientist, Clinical Research

MSD (I.A.) LLC, TW Branch · Posted Nov 9, 2026

Open

Rahway, New Jersey, United States
Hybrid
Full-time · Principal
$142K–$224K per year

Associate Principal Scientist, Clinical Research

MSD (I.A.) LLC, TW Branch · Posted Nov 9, 2026

Open

Rahway, New Jersey, United States
Hybrid
Full-time · Principal
$142K–$224K per year

Director, Clinical Research

MSD (I.A.) LLC, TW Branch · Posted Nov 9, 2026

Open

Beijing, China
Manager
10+ years

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Lead and oversee clinical research activities for the CVRM therapeutic area in China, driving strategy, execution, and compliance.

Responsibilities

Provide strategic leadership and scientific direction for CVRM clinical research
Develop and implement clinical development strategy aligned with regulatory and market needs
Oversee global clinical research program planning, execution, and management
Lead and mentor a team of clinical research professionals
Collaborate with cross‑functional teams and external partners

Requirements

Advanced degree in a relevant scientific discipline (MD, PhD)

Skills

Adaptability Clinical Development Clinical Trial Management Clinical Trial Planning Clinical Trials Monitoring Clinical Trials Operations Cross‑Cultural Awareness

Clinical Trials Coordinator

MSD · Posted Oct 30, 2026

Open

Macquarie Park, New South Wales, Australia
Full-time

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Support trial and site administration across the clinical trial lifecycle

Compensation

competitive remuneration and benefits

Responsibilities

Track essential documents and report safety reports
Ensure collation and distribution of study tools and documents
Update Clinical Trial Management Systems and tracking tools
Support clinical and non-clinical supply management
Manage labelling requirements and coordinate/sign translation change requests

Requirements

Bachelor’s degree in office management, administration, finance or healthcare

Skills

Accountability Analytical Problem Solving Clinical Data Management Clinical IT Clinical Trial Compliance Clinical Trial Documentation Clinical Trial Management

CRA Manager

MSD · Posted Nov 2, 2026

Open

Alimos, Attica, Greece
Hybrid
8–10 years

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Manage a team of CRAs, ensuring strong monitoring in clinical trials and compliance with regulations.

Compensation

We offer an attractive compensation package, outstanding benefits, and an exciting work environment with varied tasks in an international environment.

Responsibilities

Work allocation, staff development and performance appraisal
Provides input for capacity planning
Work with CRAs, PLMS and other functions to ensure consistency of processes and protocol implementation across the country
Interacts with sites to resolve operational issues
Attend local Investigator Meetings if requested

Requirements

Bachelor’s degree in Science required; advanced degree in a relevant scientific or healthcare field preferred

Skills

Adaptability Capacity Planning Clinical Research Clinical Research Management Clinical Trial Documentation Clinical Trial Management

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