[Remote] Clinical Trial Coordinator at Thermo Fisher Scientific

India

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Life SciencesIndustries

Requirements

Bachelor's degree preferred
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 2 years); in some cases, an equivalency consisting of a combination of appropriate education, training, and/or directly related experience will be considered sufficient
Ability to work in a team or independently as required
Strong organizational skills and attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Proven ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Demonstrated flexibility and adaptability to reprioritize workload and provide efficient support to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all nonclinical/clinical aspects of project implementation, execution, and closeout
Excellent communication and interpersonal skills
Excellent computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete PPD clinical training program
Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner
Able to work upright and stationary for typical working hours
Ability to use and learn standard office equipment and technology with proficiency
Able to perform successfully under pressure while prioritizing and handling multiple projects or activities
May require travel

Responsibilities

Provides administrative and technical support to the Project Team
Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document
Provides administrative support for site activation activities
Aids the development of the critical path for site activation within assigned projects in support of rapid site activations
Represents the organization in the global medical research community
May develop collaborative relationships with investigators and site personnel to conduct feasibility assessments in accordance with feasibility processes and within deliverable timelines
May develop a local knowledge base of sites in the respective market through collaboratively working with local company personnel
May utilize local knowledge, organization systems, external site lists, and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process
May act as a buddy during onboarding phase
Supports training of new staff and participates in departmental initiatives to aid in process improvements/enhancements

Skills

Key technologies and capabilities for this role

Administrative SupportTechnical SupportAudit ReadinessSite ActivationFeasibility AssessmentsInvestigator RelationsSite ListsOnboardingStaff TrainingProcess ImprovementsSOP ComplianceProject Coordination

Questions & Answers

Common questions about this position

What education and experience are required for the Clinical Trial Coordinator role?

A Bachelor's degree is preferred, along with previous experience comparable to at least 2 years that provides the necessary knowledge, skills, and abilities. Equivalency of appropriate education, training, and/or directly related experience may also be considered sufficient.

What key skills are needed for this position?

Key skills include strong organizational skills and attention to detail, ability to handle multiple tasks efficiently, flexibility to reprioritize workload, knowledge of regulations like ICH Good Clinical Practices, and excellent communication and interpersonal skills.

Is this a remote position, or does it require office work?

This is an office-based role with standard Monday-Friday hours and office environmental conditions.

What is the salary or compensation for this role?

This information is not specified in the job description.

What makes a strong candidate for the Clinical Trial Coordinator position?

Strong candidates demonstrate the ability to work in a team or independently, have proven organizational skills with attention to detail, can analyze data accurately, show flexibility in changing timelines, and possess excellent communication skills along with regulatory knowledge.

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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