Trial Management Systems jobs

Senior Medical Operations Associate

AbbVie · Posted Nov 9, 2026

Open

Sydney, New South Wales, Australia
On-site
Contract · Senior

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Senior Medical Operations Associate

AbbVie · Posted Nov 9, 2026

Open

Sydney, New South Wales, Australia
On-site
Contract · Senior

Apply with Referso

SENIOR SITE MANAGER

Johnson & Johnson · Posted Apr 8, 2025

Open

Warsaw, Masovian, Poland
Hybrid
Full-time · Mid
3–5 years

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A Senior, Site Manager is a mid-level site management role serving as the primary contact point between the Sponsor and the Investigational Site to ensure inspection readiness and compliance with clinical trial protocols, SOPs, and GCP.

Responsibilities

Acts as primary local company contact for assigned sites for specific trials
Participates in site feasibility and/or Site Qualification Visit
Attends/participates in investigator meetings and prepares materials
Executes activities within site initiation, start-up, site monitoring (on-site and remote), site management, and site/study close-out
Implements analytical risk-based monitoring model at the site level

Requirements

BA or BS degree in Pharmacy
Nursing
Life Sciences
related scientific field
Nice to have: Specific therapeutic area experience

Skills

Clinical trial monitoring GCP SOP Site management Site initiation Subject recruitment

Risk Manager (Clinical Research)

Indero · Posted Nov 7, 2026

Open

Czech Republic
Full-time · Mid
3–5 years

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The Risk Manager (Clinical Research) develops and executes risk-based monitoring strategies, ensuring data quality and integrity in clinical research projects.

Responsibilities

Provide subject matter expertise for developing and updating the risk-based monitoring strategy tailored to project needs.
Collaborate with cross-functional teams to identify and mitigate risks associated with complex indications.
Coordinate with central monitor team and verify work.
Provide budget recommendations and change orders.
Draft initial risk assessments and support the finalization of Risk Assessment and Categorization Tools (RACT).

Requirements

Bachelor’s degree in a field relevant to clinical research

Skills

Good Clinical Practice/ICH E6 (R3) Guidelines Risk-Based Monitoring strategies Risk-Based Monitoring tools MS Excel Analytical data visualization tools Lean Six Sigma

Risk Manager (Clinical Research)

Indero · Posted Nov 7, 2026

Open

Romania
Hybrid
Full-time · Senior
3+ years

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The Risk Manager (Clinical Research) plays a pivotal role in developing and executing risk-based monitoring strategies, ensuring data quality and integrity in clinical research projects, supporting Risk-Based Study Management (RBSM) principles.

Responsibilities

Provide subject matter expertise for developing and updating the risk-based monitoring strategy tailored to project needs.
Collaborate with cross-functional teams to identify and mitigate risks associated with complex indications.
Coordinate with central monitor team and verify work.
Provide budget recommendations and change orders.
Draft initial risk assessments and support the finalization of Risk Assessment and Categorization Tools (RACT).

Requirements

Bachelor’s degree in a field relevant to clinical research
Nice to have: Clinical monitoring experience
Nice to have: Data management experience
Nice to have: Drug safety experience
Nice to have: Health Canada and FDA regulations knowledge

Skills

Good Clinical Practice/ICH E6 (R3) Guidelines Risk-Based Monitoring strategies MS Excel Analytical data visualization tools

Risk Manager (Clinical Research)

Indero · Posted Nov 7, 2026

Open

Poland
Hybrid
Full-time · Senior
5+ years

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The Risk Manager (Clinical Research) plays a pivotal role in developing and executing risk-based monitoring strategies, ensuring data quality and integrity in clinical research projects.

Responsibilities

Provide subject matter expertise for developing and updating the risk-based monitoring strategy tailored to project needs.
Collaborate with cross-functional teams to identify and mitigate risks associated with complex indications.
Coordinate with central monitor team and verify work.
Provide budget recommendations and change orders.
Draft initial risk assessments and support the finalization of Risk Assessment and Categorization Tools (RACT).

Requirements

Bachelor’s degree in a field relevant to clinical research

Skills

Good Clinical Practice/ICH E6 (R3) Guidelines Risk-Based Monitoring strategies MS Excel Analytical data visualization tools Lean Six Sigma RACT tools

Senior Medical Operations Associate

Senior Medical Operations Associate

Responsibilities

Requirements

Skills

SENIOR SITE MANAGER

Responsibilities

Requirements

Skills

Risk Manager (Clinical Research)

Responsibilities

Requirements

Skills

Risk Manager (Clinical Research)

Responsibilities

Requirements

Skills

Risk Manager (Clinical Research)

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits