Referso Jobs

Senior Clinical Research Associate

Premier Research · Posted Nov 9, 2026

Open

Canada
Full-time · Senior
4+ years

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Senior Clinical Research Associate

Premier Research · Posted Nov 9, 2026

Open

Canada
Full-time · Senior
4+ years

Apply with Referso

Clinical Research Associate II

Premier Research · Posted Nov 9, 2026

Open

United States
Full-time
2+ years

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Clinical Research Associate II

Responsibilities

Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines
Maintains submission of expenses according to travel and expense requirements within company guidelines
Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements
Monitors (remote, onsite or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations
Plans day-to-day activities for monitoring a clinical study and sets priorities per site

Requirements

Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience
Nice to have: global experience

Skills

clinical trials CRA ICH GCP FDA Guidance Documents

Senior Clinical Research Associate (Contract)

Premier Research · Posted Nov 9, 2026

Open

United States
Hybrid
Contract · Senior

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The Senior Clinical Research Associate delivers quality monitoring reports and ensures data integrity and subject safety in accordance with ICH GCP/ISO14155 and regulations.

Compensation

This is a full-time contract position for 12 months.

Responsibilities

Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan (CMP) timelines
Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements
Monitors (remote, on site or other approved mode of monitoring) with a focus on data integrity and subject safety in accordance with local/regional laws and country specific regulations
Plans day-to-day activities for monitoring of a clinical study and sets priorities per site
Prepares for and conducts on site and/or remote qualification, study initiation, interim monitoring, dosing observation, and close out monitoring visits as directed per CMP

Requirements

Undergraduate degree or its international equivalent in clinical, science, or health-related field
licensed health-care professional (i.e., registered nurse)
Nice to have: Oncology
Nice to have: CNS
Nice to have: Dermatology

Skills

ICH-GCP

Clinical Research Associate

Premier Research · Posted Nov 9, 2026

Open

United States
Full-time
2+ years

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Responsible for monitoring clinical trials, ensuring data integrity, patient safety, and compliance with regulatory standards across multiple sites.

Responsibilities

Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines
Maintains submission of expenses according to travel and expense requirements within company guidelines
Responsible for the validity, correctness, and completeness of the clinical data reviewed and collected at assigned sites as dictated by ICH GCP/ISO14155, protocol and client requirements
Monitors (remote, onsite or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations
Plans day-to-day activities for monitoring a clinical study and sets priorities per site

Requirements

Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution
Licensed health-care professional (i.e., registered nurse)
Nice to have: global experience

Skills

clinical trials ICH GCP FDA Guidance Documents

Sr. Engineer Electrical Systems

Ge · Posted Nov 9, 2026

Open

Warsaw, Mazovia, Poland
Senior

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Lead electrical systems design for aeroderivative gas turbine products, driving quality, compliance, and integration across multiple product lines.

Responsibilities

Lead electrical systems design enhancements and solutions for aeroderivative gas turbine package
Design electrical layouts, sizing and specifications for LV/MV equipment
Conduct RCA and FMEA analyses
Lead design reviews for reliability, performance and safety
Ensure compliance with electrical codes and standards

Requirements

Bachelor’s degree in electrical engineering (ABET or equivalent accredited program)
Nice to have: Master’s degree in electrical engineering

Skills

generator system design electrical systems design gas turbine generator products electrical codes and standards EU directives hazardous area safety

Senior Consultant Corporate Tax - Industries

EY · Posted Nov 5, 2026

Open

Diegem, Flanders, Belgium
Senior
3+ years

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Provide tax advisory services to Belgian and foreign based companies, including cross‑border tax matters, and support clients through the full transaction life cycle.

Compensation

Attractive remuneration package - We offer an attractive remuneration package; including a company car and charging card, iPhone plus subscription, health insurance, pension plan, meal vouchers, and eco vouchers.

Responsibilities

Autonomously write standard and complex tax advice for Belgian and foreign companies
Accompany executives in client meetings and with tax authorities
Prepare proposals and external publications
Maintain client relationships and identify new opportunities
Supervise junior work and ensure quality

Requirements

Master’s degree in law or economics, potentially with a supplementary degree in fiscal matters

Skills

tax advisory cross‑border tax matters treaties WHT FTC PE

Senior to Principal Air Quality Consultant

Mott MacDonald · Posted Nov 4, 2026

Open

Düsseldorf, North Rhine-Westphalia, Germany
Hybrid
Senior

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Lead and review air quality and emissions assessments for energy and industrial infrastructure projects in Germany, providing technical and regulatory advice, managing multidisciplinary teams, and supporting business development.

Responsibilities

Lead and review air quality and emissions assessments
Provide technical and regulatory advice on BImSchG, EU directives and TA Luft
Manage multidisciplinary teams and coordinate contributions
Build and maintain client and authority relationships
Support development of junior team members

Requirements

Bachelor's or equivalent degree in Environmental Engineering, Environmental Sciences or related field
Nice to have: Experience with other countries' environmental regulations
Nice to have: Experience in business development activities
Nice to have: Experience in project management

Skills

German language proficiency English language proficiency Knowledge of BImSchG, EU directives, TA Luft Experience with air quality and emissions assessments

Senior Clinical Research Associate

Senior Clinical Research Associate

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Clinical Research Associate II

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Senior Clinical Research Associate (Contract)

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Clinical Research Associate

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Sr. Engineer Electrical Systems

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Senior Consultant Corporate Tax - Industries

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Senior to Principal Air Quality Consultant

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