Clinical Scientist

PharmiWeb.jobs: Global Life Science Jobs; London; Remote; GBP 50,000 - 80,000; Full time

Job summary

A leading biotechnology company is seeking a Clinical Scientist to design and manage clinical trials. This remote position requires an advanced degree and significant experience in clinical research. The successful candidate will collaborate with cross-functional teams to ensure compliance and integrity of clinical data.

Qualifications

• Minimum of 10 years of experience in clinical research.
• Strong understanding of regulatory requirements.
• Excellent written and verbal communication skills in English.

Responsibilities

• Design and develop clinical study protocols.
• Oversee execution of clinical trials ensuring compliance.
• Prepare and review regulatory documents for submissions.

Skills

Clinical trial design

Data analysis

Communication

Organizational skills

Education

PhD, MD, or equivalent

Tools

Microsoft Office

Clinical trial management systems (CTMS)

Job description

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Job Title: Clinical Scientist

Location: Remote (within the EU)

Contract Type: Full-Time, 12-Month Contract

Company Overview

I am currently partnered with a leading biotechnology company committed to innovative research and development in the healthcare sector. Their mission is to discover and develop groundbreaking treatments that address unmet medical needs and improve the quality of life for patients worldwide.

Position Overview

They are seeking a highly motivated and experienced Clinical Scientist to join their dynamic team. This position will play a crucial role in the design, implementation, and management of clinical trials to support our drug development programs. The successful candidate will work remotely, collaborating closely with cross-functional teams across the EU.

Key Responsibilities

1. Design and develop clinical study protocols in collaboration with clinical, regulatory, and medical teams.
2. Ensure protocols are scientifically sound, aligned with regulatory requirements, and meet the strategic objectives of the project.
3. Oversee the execution of clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
4. Monitor study progress, manage timelines, and ensure the quality and integrity of data.
5. Collaborate with biostatisticians and data management teams to analyze clinical trial data.
6. Interpret data and prepare clinical study reports, manuscripts, and presentations for internal and external stakeholders.
7. Prepare and review regulatory documents for clinical trial applications and submissions.
8. Liaise with regulatory authorities as needed to facilitate approvals and address queries.
9. Work closely with cross-functional teams, including medical affairs, regulatory affairs, pharmacovigilance, and project management.
10. Communicate study progress, findings, and issues to internal and external stakeholders.

Qualifications

1. Advanced degree (PhD, MD, or equivalent) in a relevant scientific discipline.
2. Minimum of 10 years of experience in clinical research, preferably within the biotechnology or pharmaceutical industry.
3. Strong understanding of clinical trial design, methodology, and regulatory requirements.
4. Experience in managing clinical trials across different phases (Phase I-IV).
5. Proficient in data analysis and interpretation, with a solid understanding of biostatistics.
6. Excellent written and verbal communication skills in English; proficiency in other EU languages is a plus.
7. Ability to work independently and remotely, with strong organizational and time management skills.
8. Proficient in Microsoft Office and clinical trial management systems (CTMS).

How To Apply

Interested candidates are invited to submit their resume outlining their qualifications and experience. Applications can be sent to [e-mail] with the subject line "Clinical Scientist Application".