Referso Jobs

CRA(LevelII）

Thermo Fisher Scientific · Posted Nov 10, 2026

Open

Guangdong, China
1+ years

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CRA(LevelII）

Thermo Fisher Scientific · Posted Nov 10, 2026

Open

Guangdong, China
1+ years

Apply with RefersoAI Apply on careers page

Clinical Research Associate – Level II/Sr

Thermo Fisher Scientific · Posted Jul 28, 2026

Open

Remote, Portugal
Remote
Senior
1+ years

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Clinical Research Associate responsible for monitoring and managing clinical trials, ensuring compliance with protocols and regulations, conducting on‑site and remote visits, and maintaining documentation.

Responsibilities

Monitors investigator sites using risk‑based monitoring
Applies root cause analysis and corrective actions
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates deficiencies and follows through to resolution

Requirements

Bachelor's degree in a life sciences related field
Registered Nursing certification or equivalent

Skills

Clinical monitoring Medical terminology ICH GCP knowledge Risk Based Monitoring concepts Microsoft Office English language and grammar

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FSP CRA (Level II)

Thermo Fisher Scientific · Posted Sep 9, 2026

Open

Shanghai, China
On-site
1+ years

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Clinical Research Associate (Level II) responsible for monitoring and managing clinical trial sites, ensuring compliance with protocols and regulations.

Responsibilities

Monitors investigator sites using risk-based monitoring
Ensures data accuracy through SDR, SDV and CRF review
Conducts on-site file reviews and remote monitoring activities
Escalates deficiencies and follows through to resolution
Participates in investigator meetings and site initiation

Requirements

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent

Skills

Clinical monitoring Medical terminology ICH GCP knowledge Risk Based Monitoring concepts Microsoft Office Good oral and written communication Critical thinking

SR CRA (Level II)

Thermo Fisher Scientific · Posted Oct 9, 2026

Open

Remote, Argentina
Remote
Senior
2+ years

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Senior Clinical Research Associate II responsible for monitoring investigator sites, ensuring compliance with ICH-GCP, and managing documentation and communication between sites and the client company.

Responsibilities

Monitors investigator sites with a risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Assesses investigational product through physical inventory and records review
Documents observations in reports and letters
Escalates observed deficiencies and issues to clinical management

Requirements

Bachelor's degree in a life sciences related field
Registered Nursing certification or equivalent

Skills

Basic medical/therapeutic area knowledge Medical terminology ICH GCP knowledge Risk Based Monitoring concepts Microsoft Office Critical thinking Problem solving

Trial Clinical Delivery Lead- Oncology

IQVIA · Posted Nov 5, 2026

Open

Durham, North Carolina, United States
$103K–$286K per year
10+ years

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Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out.

Compensation

The potential base pay range for this role, when annualized, is $102,500.00 - $285,500.00.

Responsibilities

Participate in bid defense preparations and lead presentations
Develop and support integrated study management plans
Accountable for strategic development and execution of clinical studies
Serve as primary project oversight and contact with customers
Set objectives for core project team

Requirements

Bachelor's Degree Life sciences or related field

Skills

advanced knowledge of job area broad knowledge of related job areas 10 years clinical research experience 6 years project management experience knowledge of clinical trials

FSP CRA I/II Gen Med - Respiratory - HIV - Oncology

Lifelancer · Posted Nov 6, 2026

Open

Remote, United States
Remote
Full-time
1+ years

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FSP Clinical Research Associate (Level I or II) responsible for remote or on‑site monitoring of clinical trials, ensuring compliance with ICH‑GCP and regulatory requirements.

Responsibilities

Monitors investigator sites with a risk‑based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Assesses investigational product through physical inventory and records review
Documents observations in reports and letters
Escalates deficiencies and issues to clinical management

Requirements

Bachelor's degree in a life sciences related field
Registered Nursing certification

Skills

clinical monitoring skills medical/therapeutic area knowledge ICH GCP knowledge root cause analysis risk based monitoring communication skills organization skills

ICH GCP knowledge jobs

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