logo inner

Senior Manager, Monitoring Oversight

4D Molecular TherapeuticsEmeryville, California, United StatesOnsite
This job is no longer open

Attention recruitment agencies:


All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.4DMT is a clinical-stage biotherapeutics company harnessing the power of directed evolution for targeted genetic medicines. We seek to unlock the full potential of gene therapy using our platform, Therapeutic Vector Evolution (TVE), which combines the power of directed evolution with our approximately one billion synthetic AAV capsid-derived sequences to invent evolved vectors for use in our products.

We believe key features of our targeted and evolved vectors will help us create targeted product candidates with improved therapeutic profiles. These profiles will allow us to treat a broad range of large market diseases, unlike most current genetic medicines that generally focus on rare or small market diseases.  Company Differentiators: •    Fully integrated clinical-phase company with internal manufacturing•    Demonstrated ability to move rapidly from idea to IND•    Five candidate products in the clinic and two declared pre-clinical programs•    Robust technology and IP foundation, including our TVE and manufacturing platforms•    Initial product safety and efficacy data substantiates the value of our platforms•    Opportunities to expand to other indications and modalities within genetic medicine

GENERAL SUMMARY: 


The Sr Manager Clinical Oversight Monitoring (COM Sr Mgr.) will be responsible for overseeing clinical monitoring activities performed by CRO and contract monitors, ensuring compliance with clinical monitoring plans, protocols, ICH/GCP guidelines, and related documents. They will work cross-functionally with stakeholders to maintain inspection readiness and monitoring quality, develop oversight processes, and SOPs. The role involves progressing the 4DMT monitoring oversight program, scaling operations across global programs, and managing organizational structure to meet regulatory and 4DMT requirements. 

RESPONSIBILITIES:  


  • Manage the 4DMT COM function globally as required

  • Collaborate with management to develop a monitoring oversight function

  • Further develop, execute, and manage the Clinical Oversight Monitoring Plan and ensure compliance with industry standards

  • Develop, utilize, and oversee metrics tools to assure the oversight activities are conducted in accordance with applicable regulations, SOPs and trial and Travere objectives

  • Interacts closely with study team throughout the lifecycle of the study.

  • Conduct QC review of monitoring visit reports, monitor visit scheduling, report completion metrics, protocol deviations, issues, and action items to identify COM, monitor, site, and study-level issues.

  • Oversee the internal process of monitoring visit report reviews by COM team and finalization metrics to assure compliance with internal and trial-specific plans

  • Proactively identify trends, issues, and risks related to monitoring and monitoring processes/plans

  • Work cross-functionally to create shared solutions

  • Ensure cross-functional understanding of applicable regulations and requirements 

  • Develop metrics as required

  • Other duties as assigned, nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time 

QUALIFICATIONS: 


Education: 

  • Bachelor’s degree or master’s degree in related Life Sciences discipline.  Equivalent combination of education and applicable job experience may be considered. 

Experience: 

  • It is preferred that the candidate have 8+ years of experience in a similar role.

  • Clinical Monitoring experience required, with a preference for Ophthalmology monitoring experience (retina experience is a definite plus)

  • Understanding of clinical trials and advanced knowledge of ICH-GCP, Clinical trials regulations, and applicable global and regional/country requirements.

  • Mastery of global regulatory requirements and guidelines 

  • Inspection experience (MHRA/EMA experience a plus)

  • Previous management experience of direct reports

  • Excellent stakeholder management skills coupled with influencing and negotiation skills

  • Understanding of resource management and organizational capacity

  • Demonstrated ability to think strategically across the organization.

Skills: 

  • The ideal candidate will embody 4DMTs core values:Dare to Cure - Break Boundaries - Beyond Yourself - Prepare & Executive Relentlessly

  • Strong interpersonal communication (written and verbal), and organizational skills

  • Able to motivate a team to work effectively under a fast-paced and changing environment

  • Strong work ethic and demonstrated ability to deliver assignments on time

  • Proficient with office automation tools, such as Microsoft Office toolkit.

  • Strong professional experience in a similar role within the pharmaceutical industry.

  • Well organized with the ability to multitask, prioritize, and manage shifting responsibilities in a dynamic, cross-functional teamwork environment.

  • Excellent collaboration skills with strong attention to detail and the ability to multi-task and manage complexity.

  • Ability to adapt to modification and changes to project plans, demonstratingflexibility to implement new strategies and tactics to accommodate these changes.

  • Ability to travel as required.  

Base salary compensation range: $114K - $181KPlease note, the base salary compensation range and actual salary offered to the final candidate depends on various factors: candidate’s geographical location, relevant work experience, skills, and years of experience.4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This job is no longer open

Life at 4D Molecular Therapeutics

The mission of 4D Molecular Therapeutics is to design and develop transformative gene therapy products using our proprietary technology to create novel adeno-associated virus variants to be utilized as treatments for serious unmet medical conditions. Our products are unlocking the full potential of gene therapy to treat, and potentially cure, genetic diseases. A large number of patients and diseases, who previously were not treatable by gene therapy, will be addressable by 4D products. 4D has one of the deepest and most diverse product pipelines in the gene therapy field. Adeno-associated virus (AAV) vectors have emerged as a favored delivery vehicle for gene therapy in the human body. They can deliver the genes for therapeutic proteins to accessible tissues in the body and are generally considered safe. Several AAV gene therapy products are in late-stage clinical development, and one product is approved in the EU (Glybera, Uniqure). However, these first-generation AAV vectors have limited utility for the majority of diseases. Many of these common AAV were discovered as laboratory contaminants and monkey infections, for example; they have not been customized as targeted medicines. In contrast, 4D customized AAV vectors, and the products made from them, are designed to unlock the full potential of gene therapy. Through 4D's Therapeutic Vector Evolution, we are able to create customized vectors solutions to overcome the hurdles identified with first-generation AAV vectors. 4D is creating the ultimate gene therapy products to cure genetic diseases using new customized delivery vehicles (vectors) to shuttle genes into the cells in any organ in the body. This 4D library of vectors will soon include several for the liver, several for the brain, several for the heart, the eye, muscle, and so on. Doctors will be able to hand pick a vector for any patient based on the organ that is diseased.
Thrive Here & What We Value1. Collaborative and innovative work environment2. Emphasis on scientific excellence and innovation3. Focus on patient outcomes and improving lives through genetic medicine4. Opportunities for career growth and professional development5. Commitment to diversity, equity, and inclusion6. Robust technology and IP foundation, including TVE and manufacturing platforms7. Initial product safety and efficacy data substantiates platform value8. Rapid progression from idea to IND9. Expanding opportunities in genetic medicine indications and modalities10. Internal manufacturing capabilities
Your tracker settings

We use cookies and similar methods to recognize visitors and remember their preferences. We also use them to measure ad campaign effectiveness, target ads and analyze site traffic. To learn more about these methods, including how to disable them, view our Cookie Policy or Privacy Policy.

By tapping `Accept`, you consent to the use of these methods by us and third parties. You can always change your tracker preferences by visiting our Cookie Policy.

logo innerThatStartupJob
Discover the best startup and their job positions, all in one place.
Copyright © 2024