Risk based monitoring concepts jobs

CRA II for FSP

Thermo Fisher Scientific · Posted Sep 8, 2026

Open

Remote, Mexico
Remote
1+ years

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CRA II for FSP

Thermo Fisher Scientific · Posted Sep 8, 2026

Open

Remote, Mexico
Remote
1+ years

Apply with Referso

CRA(Level II)

Thermo Fisher Scientific · Posted Nov 10, 2026

Open

Guangdong, China
1+ years

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Clinical Research Associate (Level II) responsible for monitoring investigator sites, ensuring compliance with ICH-GCP, managing documentation, and coordinating remote or on-site visits.

Responsibilities

Monitors investigator sites with risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates deficiencies and issues to clinical management
Maintains regular contact with investigative sites

Requirements

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

Skills

Clinical monitoring Medical/therapeutic area knowledge Medical terminology ICH GCPs Risk Based Monitoring concepts Microsoft Office Good oral and written communication

CRA(LevelII）

Thermo Fisher Scientific · Posted Nov 10, 2026

Open

Guangdong, China
1+ years

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Conduct remote or on‑site clinical monitoring and site management for pharmaceutical and biotech trials.

Responsibilities

Monitors investigator sites with a risk‑based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review
Documents observations in reports and letters
Escalates observed deficiencies and issues to clinical management
Maintains regular contact between monitoring visits and investigative sites

Requirements

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

Skills

Clinical monitoring skills Medical/therapeutic area knowledge Medical terminology ICH GCP knowledge Risk Based Monitoring concepts Critical thinking Problem solving

CRA (Level II)

Thermo Fisher Scientific · Posted Aug 6, 2026

Open

Remote, Austria
Remote
1+ years

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Clinical Research Associate (Level II) responsible for monitoring investigator sites, ensuring compliance with protocols and ICH-GCP guidelines, and managing documentation and communication with stakeholders.

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

Clinical monitoring skills Medical/therapeutic area knowledge Medical terminology ICH GCPs knowledge Risk Based Monitoring concepts Critical thinking

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

See full job description

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

Clinical Research Associate II (CRA II) – FSP Business Unit

Thermo Fisher Scientific · Posted Mar 27, 2026

Open

Remote, Romania
Remote
1+ years

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Clinical Research Associate (Level II) responsible for monitoring and site management across global clinical trials.

Responsibilities

Monitors investigator sites with a risk-based monitoring approach
Ensures data accuracy through SDR, SDV and CRF review via on-site and remote monitoring
Assesses investigational product through physical inventory and records review
Documents observations in reports and letters
Escalates deficiencies and follows issues to resolution

Requirements

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

Skills

Clinical monitoring skills Medical/therapeutic area knowledge Medical terminology Knowledge of ICH GCPs and applicable regulations Risk Based Monitoring concepts Microsoft Office proficiency

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

Senior Clinical Research Associate (Cell & Gene - FSP)

Thermo Fisher Scientific · Posted Nov 6, 2026

Open

Sydney, New South Wales, Australia +1 more
On-site
Full-time · Senior
1+ years

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Monitors investigator sites with a risk-based monitoring approach and ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.

Locations (2)

Sydney, New South Wales, Australia
Melbourne, Victoria, Australia

Compensation

We offer competitive remuneration, annual incentive plan bonus, and a range of employee benefits.

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 qualification
equivalent relevant academic or vocational qualification

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Locations (2)

Compensation

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Benefits