Cra I - Fsp - Central Scotland & North England

2+ years

Not Disclosed

Remote, USA

10 Nov. 11, 2024

Job Description

Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Clinical Research Associate (FSP)

Location: Remote/Field-based
Work Schedule: Full-Time

About Thermo Fisher Scientific:

At Thermo Fisher Scientific, you will engage in meaningful work that has a positive impact on a global scale. We empower our teams with the resources and training needed to make a difference in the world of scientific research, life-changing therapies, and clinical trials. With clinical trials conducted in over 100 countries and continuous development of novel clinical research frameworks, we deliver life-saving innovations that improve health outcomes for people and communities worldwide.

Division Overview:

PPD's Functional Service Provider (FSP) division partners with customers to provide key functional support across clinical research. As a part of our FSP team, you’ll help clients optimize their clinical trials and manage capacity while maintaining an uncompromising commitment to quality and excellence. You will join top-tier talent deployed across all engagement models, supported by state-of-the-art technology and rigorous training.

Job Summary:

As a Clinical Research Associate (CRA) at Thermo Fisher, you will be an integral part of a multinational project team, responsible for delivering exceptional customer service on complex clinical trials. You'll take full ownership of your work, thrive in a collaborative environment, and independently perform clinical monitoring activities. The role offers excellent training and opportunities for career growth within the industry.

Key Responsibilities:

Clinical Monitoring: Perform and coordinate all aspects of the clinical monitoring process for trials in compliance with ICH-GCP, EU, FDA, and local regulatory requirements.
Site Management: Conduct site visits independently, ensuring accurate data collection, informed consent process, and adherence to protocol guidelines.
Collaboration: Work closely with multidisciplinary teams to ensure successful trial outcomes, providing support to site staff and resolving queries promptly.
Training & Development: Benefit from award-winning training programs to enhance your technical and professional skills.
Customer Service: Foster strong relationships with site personnel and study teams to ensure project goals are met.

Qualifications & Skills:

Education: University degree in a life sciences field or equivalent experience.
Experience: Independent, on-site monitoring experience in a pharmaceutical or clinical research organization (CRO).
Knowledge & Abilities:
- Strong understanding of ICH-GCP, EU, and FDA requirements.
- Solid medical/therapeutic area knowledge and medical terminology.
- Exceptional communication, collaboration, and organizational skills.
- Fluency in German and English.
Time Management: Strong organizational and time management skills with the ability to manage multiple priorities simultaneously.

What We Offer:

Competitive Compensation: Competitive salary, annual incentive plan bonus, and a comprehensive benefits package.
Career Development: Thermo Fisher Scientific is committed to your growth and offers outstanding opportunities for advancement.
Innovative Culture: Join an organization that thrives on Integrity, Intensity, Innovation, and Involvement. Be part of a forward-thinking company that values diverse perspectives and ideas.

Additional Information:

Thermo Fisher Scientific is an EEO/Affirmative Action Employer, providing equal employment opportunities to all employees and applicants, irrespective of race, color, religion, sex, gender identity, sexual orientation, national origin, disability, or veteran status.

Accessibility for Applicants with Disabilities:
If you require accommodation during the job application process, please contact us at 1-855-471-2255. We are committed to providing accessible services for job seekers with disabilities.

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