Senior Clinical Scientist, Clinical Development

Biogen; Cambridge (MA); On-site; USD 141,000 - 188,000; Full time

Benefits offered by this job

Medical, Dental, Vision, & Life ins.

Disability insurance

Vacation and holidays

401(k) with match

Employee stock purchase plan

Job summary

Biogen is seeking a Senior Clinical Scientist to lead and shape clinical development strategies across programs, initially ophthalmology, with potential expansion to hematology, neurology, or immunology. You will collaborate across departments, design studies, analyze safety/efficacy data, and contribute to reports, publications, and presentations.

You will manage multiple projects, maintain regulatory awareness, and engage with investigators and key opinion leaders, traveling up to 10% for

Qualifications

• Master’s, PhD, or PharmD in a related life science or health science.
• 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.
• Proven ability to work independently and manage multiple priorities effectively.

Responsibilities

• Collaborate with the clinical development team to review, analyze, interpret, and present clinical safety and efficacy data.
• Contribute to the design and execution of clinical studies in partnership with Clinical Operations and Medical Affairs.
• Manage multiple projects across therapeutic areas, 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 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.

Skills

Biostatistics

Clinical trial design

GCP

Regulatory knowledge

Interacting with investigators

Cross-functional collaboration

Scientific writing

Independent work

Education

PhD/MD/PharmD

Advanced degree

Job description

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.

Benefits

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, 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

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.

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.