Clinical Research Coord I at Thermo Fisher Scientific

Las Vegas, Nevada, United States

Thermo Fisher Scientific Logo
Not SpecifiedCompensation
Entry Level & New GradExperience Level
Full TimeJob Type
UnknownVisa
Clinical Research, Pharmaceuticals, HealthcareIndustries

Requirements

  • Bachelor’s degree or equivalent experience in a clinical/medical field
  • BLS certificate
  • Prior experience (0 to 2 years) demonstrating necessary knowledge, skills, and abilities, or comparable combination of education, training, and/or directly relevant experience
  • Basic understanding of clinical research processes, including GCP, SOPs, informed consent, and safety monitoring
  • Ability to work autonomously, evaluate data, and prioritize intricate information with meticulousness
  • Proven ability to exercise discretion, good judgment, decision-making, negotiation, and influencing skills
  • Strong communication skills and proficiency in English
  • Excellent organizational skills
  • Proficiency in basic computer applications
  • Strong interpersonal skills to work effectively in a team environment
  • Capability to remain in a vertical or fixed position for 6-8 hours daily
  • Ability to perform repetitive hand movements and frequent mobility
  • Occasional crouching, stooping, frequent bending, and twisting of upper body and neck
  • Ability to lift and carry objects up to 15-20 lbs
  • Ability to use various computer software applications
  • Strong ability to communicate, understand information, interact with diverse groups, perform under stress, and multitask
  • Regular and consistent attendance

Responsibilities

  • Conduct at least one ongoing clinical trial involving patients or healthy volunteers
  • Interact with research site team and interdepartmental staff to ensure positive interactions with patients at site for study planning, from initiation to closeout
  • Conduct clinical studies in strict adherence to FDA/GCP and ICH regulations, ensuring patient safety and providing medical care to patients
  • Perform study activities, including informed consent, screening, and protocol procedures (vital signs, pregnancy tests, height, weight, ECGs)
  • Accurately record patient information and test results, complete IP accountability logs, and report non-compliance
  • Ensure IRB approval and compliance
  • Promote the company and build positive patient relationships
  • Manage patient bookings, follow-up calls, and log information on sponsor systems
  • Gather source documents and update patient files
  • Adhere to company standards and maintain a neat facility appearance

Skills

GCP
ICH regulations
FDA regulations
Informed Consent
Patient Screening
Vital Signs
ECG
IRB compliance
Clinical Trial Management
Source Documentation
Patient Recruitment

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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