Join Beacon Therapeutics (USA) Inc as an Associate Medical Director/Medical Director in Clinical Science and lead groundbreaking initiatives in the Biotech industry. This fully remote position allows you to work from home, fostering a flexible work-life balance while making remarkable contributions to innovative healthcare solutions. You will collaborate with a diverse and talented team passionate about advancing clinical science, all while upholding our core values of accountability, integrity, and continuous improvement.

Your expertise will directly impact patient outcomes and drive research projects that push the boundaries of science. Embrace the opportunity to engage in a forward-thinking environment where your insights can shape the future of therapeutics. You will receive 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 provided STD & LTD. Be a part of a culture that values transparency and respect, where your voice is heard and your contributions truly matter.

Who are we? An Introduction

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-national 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.

Your day as aN Associate Medical Director/Medical Director Clinical Science

As the Associate Medical Director or Medical Director of Clinical Science at Beacon Therapeutics (USA) Inc, you will be pivotal in shaping the future of ophthalmology through the design, implementation, and execution of groundbreaking clinical trials. In this role, you will collaborate closely with cross-functional teams, ensuring seamless integration of expertise from various disciplines. Your leadership will guide the strategic direction of clinical studies, focusing on innovative approaches that enhance patient care and improve therapeutic outcomes. With your deep understanding of ophthalmology, you will contribute to the advancement of clinical methodologies and regulatory submissions, all while fostering an environment of teamwork and continuous improvement.

This position offers a unique opportunity to make a meaningful impact in a rapidly evolving field, while working remotely within a professional and respectful culture.

Are you a good fit for this Associate Medical Director/Medical Director Clinical Science - REMOTE job?

To excel as the Associate Medical Director or Medical Director of Clinical Science at Beacon Therapeutics (USA) Inc, candidates must possess a robust set of skills and expertise. Proficiency in analytical and data interpretation is crucial, enabling you to review, clean, and interpret clinical and safety data effectively. A strong foundation in clinical development is necessary, with knowledge of clinical trial design, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and regulatory requirements from entities such as the FDA and EMA.

Successful candidates will demonstrate exceptional cross-functional collaboration and communication skills, working seamlessly with teams in medical affairs, clinical operations, biostatistics, and regulatory compliance. High integrity, autonomy, and motivation are key personal attributes, complemented by a quality-focused and well-organized work ethic. Excellent written and verbal communication skills are essential for presenting clinical findings and facilitating scientific discussions, alongside demonstrated strategic and critical thinking capabilities.

Knowledge And Skills Required For The Position Are

Analytical and data interpretation skills - ability to review, clean and interpret clinical and safety data. Strong clinical development knowledge a solid understanding of clinical trial design GCP ICH guidelines, regulatory requirements (FDA/EMA) a to support protocol development data review data analysis and AE reporting. Cross-functional Collaboration and communication 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 High level of integrity autonomy and motivation Quality focused and well-organized Excellent written and verbal communication skills Demonstrated strategic and critical thinking

Your next step

Applying for this position is a walk in the park if you feel it's a good fit for you. Best of luck! #J-18808-Ljbffr