Not SpecifiedCompensation
Entry Level & New GradExperience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Biotechnology, Clinical ResearchIndustries

Position Overview

  • Location Type: Not Specified
  • Job Type: Full time
  • Work Schedule: Standard (Mon-Fri)
  • Environmental Conditions: Office
  • Salary: Not Specified

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Summarized Purpose: Performs remote activities on assigned projects in liaison with the Remote CRA, On-Site CRA and study CTM. Provides support with regards to site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines. May be assigned limited site contact activities during study start-up, site management, recruitment and close out phases.

Key Responsibilities

  • Completes study and site management activities as defined in task matrix, and as applicable and advised for study assigned.
  • Completes and documents study-specific training.
  • Orients and trains on any CRG/study-specific systems.
  • Provides in-house support during pre-study assessments and with pre-study assessment waivers, as agreed for project.
  • Supports to customize Site ICF with site contact details, as needed.
  • Performs remote review of EMR/EHR checklist and supports collection, as applicable assessments.
  • Verifies document collection and RCR submission status; updates site EDL and verifies site information.
  • Reviews patient facing materials and review translations, as directed.
  • Supports site staff with the vendor related qualification process, where applicable.
  • Provides support by ensuring system access is requested/granted and revoked for relevant site staff during pre-activation and subsequent course of the study.
  • Provides support to follow-up on site staff training, as applicable.
  • Coordinates and supports logistics for IM attendance, as advised.
  • Supports maintenance of vendor trackers, as advised.
  • Coordinates study/site supply management during pre-activation and subsequent course of the study.
  • Supports Crucial Document collection, review and updating in systems, as applicable.
  • Follows up and supports on missing study vendor data like ECGs, lab samples, and e-diaries, as advised.
  • Supports ongoing remote review of centralized monitoring tools, as advised.
  • Supports Site payments processes by coordinating with various functional departments within organization and site.
  • Supports system updates and reconciliations, as advised and follows-up on site invoices throughout the study period.
  • Performs reconciliation tasks on assigned trials including but not limited to CRF and query status, deviations, SAEs and safety reports, as applicable.
  • Verifies document collection status in CRG systems and drives action for missing/incomplete/expired documents and open document findings, as advised.
  • May perform other assigned site management tasks, as directed by RCRA and as per Task Matrix.
  • May perform a specific role profile for FSP opportunities according to Client requests.
  • Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.

Keys to Success

  • Education and Experience: Bachelor's degree or equivalent and relevant formal academic / vocational qualification.
  • Experience: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
  • Knowledge, Skills and Abilities: Basic medic

Skills

Remote Monitoring
Clinical Trial Support
Site Management
Regulatory Compliance
EMR/EHR Review
Documentation
Training and Orientation

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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