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Senior Clinical Scientist - Remote

ZipRecruiter

Cambridge

Remote

GBP 60,000 - 80,000

Full time

30+ days ago

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Job summary

An established industry player in biotech is seeking a Senior Clinical Scientist to join their innovative team. This fully remote role offers the chance to contribute to groundbreaking clinical programs and enhance patient care through rigorous data analysis and collaboration with cross-functional teams. You will play a pivotal role in designing and executing clinical trials while ensuring compliance with regulatory standards. With a commitment to scientific excellence and a culture that values integrity, this opportunity allows you to make a meaningful impact in the field of healthcare. If you are passionate about advancing clinical science and improving patient outcomes, this role is perfect for you!

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k)
Life Insurance
Health Savings Account
Flexible Spending Account
Paid Time Off
Employee Discounts
Employer paid STD/LTD

Qualifications

  • Strong foundation in clinical regulatory and pharmacovigilance knowledge.
  • Ability to collaborate and communicate across cross-functional teams.

Responsibilities

  • Design, execute, and analyze clinical trials ensuring data integrity.
  • Support protocol development and engage in scientific discussions.

Skills

Clinical regulatory knowledge
Pharmacovigilance knowledge
Clinical trial design
Analytical skills
Data interpretation skills
Cross-functional collaboration
Communication skills

Job description

Job Description

Join Beacon Therapeutics (USA) Inc as a Senior Clinical Scientist (REMOTE) and immerse yourself in cutting-edge biotech research that is shaping the future of healthcare. This fully remote position allows you to collaborate with a diverse team of forward-thinking professionals committed to making remarkable advancements in clinical science. Your expertise will play a crucial role in driving critical projects, facilitating continuous improvement, and enhancing patient outcomes.

At Beacon Therapeutics, accountability and integrity are at the heart of our work culture, empowering you to make impactful contributions from anywhere. Embrace the opportunity to work collaboratively and transparently with talented individuals who share your passion for innovation. You can get great benefits such as Medical, Dental, Vision, 401(k), Life Insurance, Health Savings Account, Flexible Spending Account, Competitive Salary, Paid Time Off, Employee Discounts, and Employer paid STD/LTD. If you are ready to take the next step in your career and drive meaningful change, we encourage you to apply today!

Hello, we're Beacon Therapeutics (USA) Inc

If you are passionate about gene therapy and its ability to enhance the lives of patients, then Beacon is a great team to join. We are a diverse, multi-team of talented people all working together at our sites in the US and the UK, or as a remote contributor. Everyone here, whatever their role or location, plays a genuine part in bringing our treatments to patients. Everyone has a voice, and every contribution makes a difference.

What would you do as a Senior Clinical Scientist

As a Senior Clinical Scientist at Beacon Therapeutics (USA) Inc, you will play a pivotal role in advancing our innovative clinical programs. Collaborating with cross-functional teams, you will design, execute, and analyze clinical trials, ensuring the highest standards of data integrity, regulatory compliance, and scientific rigor. Your expertise will support protocol development, safety monitoring, and the interpretation of medical data, while also driving pharmacovigilance activities. This multifaceted position offers you the chance to influence trial outcomes and contribute to groundbreaking research that enhances patient care and therapeutic effectiveness.

Join us and be part of a professional team dedicated to making remarkable achievements in the biotech industry.

Does this sound like you?

To excel as a Senior Clinical Scientist at Beacon Therapeutics (USA) Inc, you will need a robust skill set that aligns with our commitment to scientific excellence. A strong foundation in clinical regulatory and pharmacovigilance knowledge is essential, along with a solid understanding of clinical trial design and regulatory requirements, including GCP and ICH guidelines as set forth by the FDA and EMA. Your analytical and data interpretation skills will enable you to review, clean, and interpret complex clinical and safety data effectively. Furthermore, the ability to collaborate and communicate across cross-functional teams, including medical affairs, clinical operations, biostatistics, and regulatory and safety departments, is critical.

You will be expected to present clinical findings and engage in scientific discussions with both internal and external stakeholders, ensuring that our studies uphold the highest standards of integrity and rigor.

Knowledge and skills required for the position are:

  • Strong clinical regulatory and pharmacovigilance knowledge
  • A solid understanding of clinical trial design
  • Working knowledge of GCP ICH guidelines regulatory requirements (FDA, EMA) and pharmacovigilance principles to support protocol development, data analysis, and AE reporting.
  • Analytical and data interpretation skills with ability to review, clean, and interpret clinical and safety data.
  • Cross-functional collaboration and communication - a strong ability to work with medical affairs, clinical operations, biostatistics, regulatory, and safety, effectively presenting clinical findings and supporting scientific discussions with internal and external stakeholders.

Are you ready for an exciting opportunity?

If you believe that this position matches your requirements, applying for it is a breeze. Best of luck!

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