Description
Job Location: London, UK
Job Location Type: Remote
Job Contract Type: Contract
Job Seniority Level: Mid-Senior level
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
- Design and develop clinical study protocols in collaboration with clinical, regulatory, and medical teams.
- Ensure protocols are scientifically sound, aligned with regulatory requirements, and meet the strategic objectives of the project.
- Oversee the execution of clinical trials, ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Monitor study progress, manage timelines, and ensure the quality and integrity of data.
- Collaborate with biostatisticians and data management teams to analyze clinical trial data.
- Interpret data and prepare clinical study reports, manuscripts, and presentations for internal and external stakeholders.
- Prepare and review regulatory documents for clinical trial applications and submissions.
- Liaise with regulatory authorities as needed to facilitate approvals and address queries.
- Work closely with cross-functional teams including medical affairs, regulatory affairs, pharmacovigilance, project management.
- Communicate study progress findings issues to internal external stakeholders.
Qualifications
- Advanced degree (PhD MD or equivalent) in a relevant scientific discipline.
- Minimum of 10 years experience in clinical research preferably within biotechnology or pharmaceutical industry.
- Strong understanding of clinical trial design methodology regulatory requirements.
- Experience managing clinical trials across different phases (Phase I-IV).
- Proficient in data analysis interpretation solid understanding biostatistics.
- Excellent written verbal communication skills English; proficiency other EU languages is a plus.
- Ability work independently remotely strong organizational time management skills.
- Proficient Microsoft Office clinical trial management systems (CTMS).
How To Apply
Interested candidates are invited to submit their resume outlining their qualifications experience Applications can be sent to [email] with subject line "Clinical Scientist Application".
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