Senior Data Manager - Clinical Data
- Employer
- 4D Molecular Therapeutics
- Location
- Emeryville, California
- Start date
- Sep 22, 2024
View more categoriesView less categories
- Discipline
- Clinical, Clinical Data, Clinical Research
- Required Education
- Bachelors Degree
- Position Type
- Full time
- Hotbed
- Biotech Bay, Best Places to Work
Job Details
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
SUMMARY:
The Sr. Data Manager will be responsible for performing or overseeing vendors to perform Data Management operational end-to-end activities and participate as an active member in a cross-function study team to plan, lead, and execute tasks required for assigned clinical studies across all phases. The Senior Data Manager has a broad, fundamental knowledge of the data management process and can perform most required tasks with minimal guidance.
Data management is one of the essential functions of the Clinical Development organization at 4DMT. Together with the other two functions within the Data Science group, Biostatistics, and Statistical Programming, we provide critical support for the company’s clinical development programs in gene therapies for retina diseases and other therapeutic areas.
RESPONSIBILITIES:
- Lead Data Management of a clinical study or a series of related studies with minimal guidance
- Manage and monitor the progress of data management activities with CROs, vendors, and stats/programming groups on assigned studies
- Review protocols for appropriate data capture, including electronic Case Report Form (eCRF) design.
- Perform a thoroughly detailed review of eCRF data requirements.
- Lead the development of data edit check specifications and data listings
- Coordinate Electronic Data Capture (EDC) system design and testing according to company standards.
- Develop or lead the development of the Data Management and Data Transfer Plan for assigned clinical studies.
- Attend study meetings and provide Data Management updates and metrics.
- Review and provide feedback to the clinical team on other study documents, e.g., Clinical Monitoring plans, Statistical Analysis Plans, and vendor specifications
- Provide training on the EDC system and/or eCRF Completion Guidelines to internal and external study team members as needed
- Perform or ensure assigned CRO reconciliation of header data from external data sources against the clinical database
- Perform or ensure assigned CRO completed Serious Adverse Event reconciliation activities according to SOPs and guidelines
- Lead database upgrades/migrations, including performing User Acceptance Testing
- Maintain data management files / eTMF
- Perform and coordinate database interim snapshot, lock, and freeze activities
- 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 higher (life-science-related fields preferred)
Experience:
- 6+ years of data management experience in the biotech/pharmaceutical industry or clinical data management service providers. Of which at least three (3+) years in a lead study data manager role.
- Experience in retina diseases and/or gene therapies a plus.
- Hands-on operational experience as Data Management Lead in all phases of clinical trials, including development/deployment/validation/maintenance/closeout of a clinical database, coordination of data transfers/reconciliations, training on data management systems, etc.
- Experience in vendor management and performance assessments
- In-depth knowledge and expertise with CDISC data standards and models.
- Proficient in using clinical data management systems (e.g., Medidata Rave) and the data flow, including those from external sources (IRT, safety, central/specialty labs, reading centers, PROs, etc.)
- Proficiency in data management process and knowledge of Good Clinical Data Management Practices (GCDMP) in global clinical trials
- Knowledge of ICH GCP and other applicable regulatory rules and guidelines.
- Knowledge of the clinical development process.
Skills:
- Proficient with MS Office (Word, Excel, PowerPoint, etc.)
- Excellent interpersonal communication skills (written and verbal)
- Innate collaborative attitude, with demonstrated ability to work effectively in a small company environment that moves at a tremendous pace.
- Excellent organization and project/time management skills
- Ability to multitask in a high-volume environment with shifting priority and conflicting deadlines
- Proven conceptual, analytical and strategic thinking
- Excellent attention to details
Base salary compensation range $164,000 - $196,000
Please note: the base salary compensation range and actual salary offered to the final candidate depends on various factors: 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 DisabilitiesCompany
4DMT is a gene therapy company with a transformative discovery platform --Therapeutic Vector Evolution --that enables our “disease first” approach to product discovery and development, thereby allowing us to customize our AAV vectors to target specific tissue types associated with the underlying disease.
At 4DMT we are creating and developing optimized “biopharmaceutical grade” AAV vectors that will allow us uniquely to unlock the full potential of gene therapy. Our customized and proprietary AAV vectors are each designed, according to a 4DMT Target Vector Profile, to deliver genes to specific cells and tissues in the body to eradicate both rare and large market diseases.
While AAV gene therapy pioneers are making great strides with the first wave of products, hurdles still exist with the use of conventional vectors. The most commonly used AAV capsids (e.g., AAV2, 5, 8 and 9) were identified either 1) as contaminants in lab stocks of adenovirus, or 2) through monkey tissue processing. Therefore, these conventional vectors are not targeted specifically to any tissue in the body. This can lead to inefficient and non-specific delivery, thus requiring extremely high doses and potentially resulting in toxicities (including inflammation), high manufacturing burdens and suboptimal efficacy. In addition, suboptimal routes of delivery can be required for delivery to the right tissues (e.g., subretinal delivery to the retina). Finally, pre-existing neutralizing antibodies in many patients can limit efficacy, clinical trial enrollment and market sizes. 4DMT Innovation empowers us to create new and improved next generation AAV capsids to allow targeted delivery of our products by the optimal clinical route of administration.
At 4DMT we use our robust discovery platform, termed “Therapeutic Vector Evolution,” to create customized and proprietary gene delivery vehicles (novel AAV vectors) to deliver genes to specific tissues and cells in the body by the optimal route of administration. We use the power of evolution to create and refine these optimized vectors through genetic diversification and then natural selection in vivo.
4D Purpose Statement: Boldly Innovating to Unlock the Full Potential of Gene Therapy for Countless Patients
GUIDING PRINCIPLES
- Dare to Cure - Patients are waiting. Create big dreams for patients and take calculated risks to achieve them
- Break Boundaries - Question the status quo and innovate beyond conventional approaches
- Beyond Yourself - It's about patients, their families, our team, our families. We strengthen each other.
- Prepare and Execute Relentlessly - Start with the end in mind, over-prepare and make contingency plans to your contingency plans
We invite all of you who share our passion and vision in creating the ultimate gene therapy products to cure genetic and rare diseases in children and adults. We seek the best people in the industry who identify with our mission and innovative results-driven approach. We offer an inspiring and collaborative environment that encourages individual contributions, recognizes performance in multiple ways, offers generous benefits and provides challenging opportunities for career development.
- Website
- http://www.4dmoleculartherapeutics.com/
- Phone
- 510-505-2680
- Location
-
5858 Horton St. Suite 455
Emeryville
California
94608
United States
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