This job is expired.

Associate Director, Clinical Trial Lead

South San Francisco, CA
Full-Time

Job Description

Job Description

About This Role

Make the most meaningful impact of your career in this rewarding role with Biogen, a well established pioneer in the pharmaceutical industry. This is your rare opportunity to transcend day-to-day management operations as you design operational strategy and oversee our clinical research organization (CRO) partners to develop clear protocol concepts and final protocols. The best part: You will own responsibility for entire clinical trial studies, including operational design, successful delivery, and the positive impact on the lives of patients with a wide array of conditions, including nephrotic conditions, multiple sclerosis (MS), Alzheimer's disease, and spinal muscular atrophy (SMA). Working from home, office, or both on a flexible, hybrid schedule, you'll have the support of a team with well-established procedures in place to make your vision a reality.

What You'll Do

  • Develop and oversee implementation of the study-level operational strategy for the successful delivery of clinical studies.
  • Chair the Clinical Study Team (CST) to drive development of scientifically robust, operationally feasible, and clear concepts/protocols.
  • Oversee delivery of studies by CROs to ensure quality execution in line with time and budget forecasts.
  • Partner with the CRO SMT lead to ensure the CRO creates appropriate risk-mitigation plans and effectively identifies/resolves issues.
  • Establish and drive efficient team operations by establishing an open culture defined by communication, goal setting, and oversight of strategy implementation.
  • Ensure effective, consistent, efficient and compliant processes.
  • Champion synergies among other studies, programs, and development units to enhance excellence in study planning and execution.

Who You Are

Scientifically and clinically astute, you're a mission-driven individual with the strategic vision to see the big picture and assume responsibilities much broader and more meaningful than day-to-day operations. Decisive, analytical and self-confident, you are determined to own all of your career and the difference you can make on the lives of others through your leadership and ability to inspire excellence.

Qualifications

Required Skills

  • Bachelors Degree in a scientific discipline
  • 8 + years in clinical operations management, overseeing outsourced clinical trials per quality, timeline, and budget expectations, preferably with a sponsor company and/or a CRO
  • Related scientific and clinical expertise and exceptional project-management, risk-assessment, contingency-planning, and communication skills
  • Extensive knowledge of clinical development related to one or more trial phases (I, II, III, or IV), as well as cross-functional drug development
  • Unquestioned expertise in Good Clinical Practices (GCP), International Council for Harmonisation (ICH) guidelines and regulatory requirements for clinical development
  • Ability to establish operational plans and support the CRO in executing them
  • Effective CRO management skills and ability to adapt to the Global Clinical Operations (GCO) outsourcing model

Preferred Skills

  • Experience operationalizing nephrology clinical studies
  • An advanced degree, such as a master's or PhD in a related field
  • Investigator site and/or monitoring experience

Additional Information

The base compensation range for this role is $172,000-237,000. Base salary offered is determined though 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 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 our DE&I efforts.

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.

 

PDN-9ec9d02e-d93d-4fea-9ce2-04077ef57e91

Job Description

About This Role

Make the most meaningful impact of your career in this rewarding role with Biogen, a well established pioneer in the pharmaceutical industry. This is your rare opportunity to transcend day-to-day management operations as you design operational strategy and oversee our clinical research organization (CRO) partners to develop clear protocol concepts and final protocols. The best part: You will own responsibility for entire clinical trial studies, including operational design, successful delivery, and the positive impact on the lives of patients with a wide array of conditions, including nephrotic conditions, multiple sclerosis (MS), Alzheimer's disease, and spinal muscular atrophy (SMA). Working from home, office, or both on a flexible, hybrid schedule, you'll have the support of a team with well-established procedures in place to make your vision a reality.

What You'll Do

  • Develop and oversee implementation of the study-level operational strategy for the successful delivery of clinical studies.
  • Chair the Clinical Study Team (CST) to drive development of scientifically robust, operationally feasible, and clear concepts/protocols.
  • Oversee delivery of studies by CROs to ensure quality execution in line with time and budget forecasts.
  • Partner with the CRO SMT lead to ensure the CRO creates appropriate risk-mitigation plans and effectively identifies/resolves issues.
  • Establish and drive efficient team operations by establishing an open culture defined by communication, goal setting, and oversight of strategy implementation.
  • Ensure effective, consistent, efficient and compliant processes.
  • Champion synergies among other studies, programs, and development units to enhance excellence in study planning and execution.

Who You Are

Scientifically and clinically astute, you're a mission-driven individual with the strategic vision to see the big picture and assume responsibilities much broader and more meaningful than day-to-day operations. Decisive, analytical and self-confident, you are determined to own all of your career and the difference you can make on the lives of others through your leadership and ability to inspire excellence.

Qualifications

Required Skills

  • Bachelors Degree in a scientific discipline
  • 8 + years in clinical operations management, overseeing outsourced clinical trials per quality, timeline, and budget expectations, preferably with a sponsor company and/or a CRO
  • Related scientific and clinical expertise and exceptional project-management, risk-assessment, contingency-planning, and communication skills
  • Extensive knowledge of clinical development related to one or more trial phases (I, II, III, or IV), as well as cross-functional drug development
  • Unquestioned expertise in Good Clinical Practices (GCP), International Council for Harmonisation (ICH) guidelines and regulatory requirements for clinical development
  • Ability to establish operational plans and support the CRO in executing them
  • Effective CRO management skills and ability to adapt to the Global Clinical Operations (GCO) outsourcing model

Preferred Skills

  • Experience operationalizing nephrology clinical studies
  • An advanced degree, such as a master's or PhD in a related field
  • Investigator site and/or monitoring experience

Additional Information

The base compensation range for this role is $172,000-237,000. Base salary offered is determined though 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 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 our DE&I efforts.

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.

 

PDN-9ec9d02e-d93d-4fea-9ce2-04077ef57e91

About Biogen

Biogen Inc. is an American multinational biotechnology company based in Cambridge, Massachusetts, specializing in the discovery, development, and delivery of therapies for the treatment of neurological diseases to patients worldwide.

Related Jobs

Apply For This Job
Associate Director, Clinical Trial Lead
Biogen
South San Francisco, CA
Apr 29, 2025
Full-time
Your Information
First Name *
Last Name *
Email Address *
This email belongs to another account. Please use a diferent email address or Sign In.
Zip Code *
Password *
Confirm Password *
Create your Profile from your Resume
By clicking the Apply button, you agree to the terms of use and privacy policy and consent to receive emails from us about job opportunities, career resources, and other relevant updates. You can unsubscribe at any time.
Supercharge Your Resume with AI

Boost your resume with AI-driven enhancements. The tool analyzes and refines your content, highlighting your strengths and tailoring it for maximum impact. Get personalized suggestions and apply improvements instantly to stand out in the job market.

©2025 International Association of Women.
Powered by TalentAlly.