FSP CRA II at Thermo Fisher Scientific

Beijing, Beijing, China

Thermo Fisher Scientific Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, Pharmaceuticals, HealthcareIndustries

Requirements

  • Applies root cause analysis (RCA), critical thinking and problem-solving skills
  • Knowledge of protocol compliance, ICH-GCP guidelines, applicable regulations, and SOPs
  • Ability to conduct remote or on-site visits and manage documentation
  • Familiarity with risk-based monitoring approach
  • Proficiency in data review processes (SDR, SDV, CRF)
  • Skills in business writing standards for reports and letters
  • Experience with investigational product accountability (inventory and records)
  • Ability to manage procedures and guidelines from sponsors/supervising environments (FSO, FSP, Government, etc.)
  • Competence in study systems (e.g., CTMS) and QC checks

Responsibilities

  • Monitors investigator sites using risk-based monitoring: applies RCA, identifies site process failures, and implements corrective/preventive actions
  • Ensures data accuracy through SDR, SDV, and CRF review via on-site and remote activities
  • Assesses investigational product through physical inventory and records review
  • Documents observations in reports and letters timely using approved standards
  • Escalates deficiencies/issues to clinical management and follows through to resolution
  • Maintains regular contact with sites between visits to ensure protocol adherence, issue resolution, and timely data recording
  • Conducts supervising tasks per approved monitoring plan
  • Participates in investigator payment process
  • Shares responsibility with project team on issues/findings resolution and investigates/follows up as applicable
  • Provides trial status tracking and progress update reports to CTM
  • Updates study systems (e.g., CTMS) per conventions and performs QC checks on reports
  • Participates in investigator meetings
  • Identifies potential investigators in collaboration with client
  • Initiates clinical trial sites per procedures, ensuring compliance and making recommendations
  • Ensures trial close-out and retrieval of materials
  • Verifies crucial documents are complete per ICH-GCP and regulations; conducts on-site file reviews
  • Contributes to project team by assisting in publications/tools and sharing ideas
  • Performs additional study tasks as assigned by CTM

Skills

Clinical Monitoring
Site Management
ICH-GCP
Risk-Based Monitoring
Root Cause Analysis
SDV
SDR
Protocol Compliance
Regulatory Compliance
SOPs

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters
1956Year Founded
$17MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.
Sale of anatomical pathology business could create a temporary product gap.
Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.
Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.
They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.
Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.
Collaboration with Mainz Biomed positions them in the growing cancer detection market.

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