Senior Clinical Scientist, Clinical Development

Biogen, Inc.; Cambridge (MA); In loco; USD 141.000 - 188.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical, Dental, Vision Insurance

Life insurance

401(k) with company matching

Tuition reimbursement

Descrizione del lavoro

Biogen is seeking a Senior Clinical Scientist to contribute to clinical strategy and execution across ophthalmology programs, with potential expansion into immunology, hematology, or neurology. You will collaborate across Clinical Development to provide scientific expertise and shape program decisions while advancing patient outcomes.

The role requires a strong track record in clinical development, data interpretation, and publication activities, with travel up to 10% to field sites and

Competenze

• Requires advanced degree in life/health science and at least 6 years in clinical development.
• Experience with ophthalmology and preferably immunology/hematology/neurology is desired.
• Strong analytical skills and ability to translate data into actionable insights.

Mansioni

• Review and interpret clinical safety and efficacy data across programs.
• Design and execution of clinical studies in collaboration with Operations and Medical Affairs.
• Manage multiple projects across therapeutic areas with cross-functional input.
• Support clinical data reviews, data cleaning, and study reporting.

Conoscenze

Biostatistics

Clinical trial design

GCP

Regulatory requirements

Ophthalmology

Interacting with investigators

Cross-functional collaboration

Scientific writing

Formazione

Master’s/PhD/ PharmD in a life/health science

Descrizione del lavoro

About This Role

As a Senior Clinical Scientist, you will be an integral member of the clinical development team, significantly contributing to the development and execution of clinical strategies across various programs. Initially focusing on ophthalmology, your expertise may later extend to hematology, neurology, or immunology indications. In this role, you will collaborate across the clinical development organization, providing scientific and medical expertise, and contributing strategically and scientifically to both current and future clinical programs. Your work will be vital in guiding evidence-based program decisions and ensuring the successful progression of clinical studies. This position offers the opportunity to influence the clinical development landscape and make a tangible impact on patient outcomes.

What You’ll Do

• Collaborate with the clinical development team to accurately review, analyze, interpret, and present clinical safety and efficacy data.
• Contribute to the design and execution of clinical studies in partnership with various departments including Clinical Operations and Medical Affairs.
• Manage multiple projects across therapeutic areas, independently prioritizing deliverables and coordinating cross-functional input.
• Support clinical database lock activities, including data review and cleaning, and contribute to clinical study reports.
• Remain up to date on current regulations, relevant guidelines, and scientific advances.
• Facilitate collaboration with Translational Medicine for transitioning research stage assets to clinical development.
• Develop clinical study reports, manuscripts, abstracts, scientific publications, and conference presentations.
• Provide scientific support for advisory boards, consultant meetings, and investigator meetings.
• Cultivate relationships with external partners such as clinical investigators and key opinion leaders.
• May include up to 10% of travel to field sites, internal and external meetings, and conferences.

Who You Are

You possess a strong scientific acumen and have a proven track record in clinical development. Your ability to analyze complex clinical data and translate it into actionable insights sets you apart. You are driven by a passion for advancing medical science and thrive in collaborative environments where your expertise can shape strategic decisions. With excellent communication skills, you effectively engage with diverse stakeholders, nurturing relationships that enhance innovation and business growth. Your proactive approach and adaptability allow you to navigate the dynamic landscape of clinical development seamlessly.

Required Skills

• Master’s, PhD, or PharmD in a related life science or health science discipline.
• At least 6 years of clinical development experience in the pharmaceutical or biotechnology industry.
• Strongly preferred experience in ophthalmology; preferred experience in immunology, hematology, or neurology.
• Demonstrated experience in analyzing and interpreting clinical safety and efficacy data.
• Working knowledge of biostatistics, clinical trial design, GCP, and regulatory requirements.
• Experience interacting with clinical investigators and medical experts.
• Experience in a cross-functional clinical development role.
• Familiarity with scientific writing and publication processes.
• Proven ability to work independently and manage multiple priorities effectively.

Job Level

Management

Additional Information

The base compensation range for this role is: $141,000.00-$188,250.00. Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity. Regular employees are eligible to receive both short term and long term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.

• In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to: Medical, Dental, Vision, & Life insurances Fitness & Wellness programs including a fitness reimbursement Short- and Long-Term Disability insurance A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit 401(k) program participation with company matched contributions Employee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participation

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law.

Biogen is an E-Verify Employer in the United States.

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.

As Biogen recently acquired Apellis, you can find additional open jobs on our Apellis website here.