Job Description
Job Description
Description :
- Note : exact level depending on experience
Company Overview :
Vividion is a next generation biotechnology company based in San Diego that is leveraging its proprietary chemical proteomics platform to conduct proteome-wide footprinting of drug-protein interactions with unprecedented breadth and precision. Our technology allows us to screen, identify and optimize novel drugs that selectively bind virtually any protein, including proteins previously considered “undruggable”. Our pipeline and emerging programs reflect a matured and productive platform capable of delivering first in class drugs utilizing novel mechanisms of action (allosteric inhibitors, protein-protein interaction inhibitors, functional activators, degraders etc.) against undruggable targets in the oncology and immunology space.
We prize scientific excellence, creativity, team players and we are committed to continued innovation. We have worked hard to create a collaborative and dynamic work culture where your ideas and discoveries are valued and will have an impact. We are growing and there are opportunities for mentorship and career progression.
Vividion has been recognized as a Top Workplace by The San Diego Union-Tribune in 2022, 2023, and 2024.
Job Summary :
The Associate Director / Director, Clinical Operations will provide clinical operations strategy, planning, initiation, and execution of clinical trials, including vendor selection, contracts and budgets, vendor oversight and management, and proactive risk identification to ensure on-time delivery of quality trials that meet the highest level of compliance.
Requirements :
Essential Duties and Responsibilities :
Oversee tactical implementation of the clinical development plan by managing the timeline, resources, and budget of clinical studiesContribute to execution strategy of clinical programs and work collaboratively with the clinical operations group and cross functional team to ensure successful implementation of clinical trialsLead clinical studies and provide strategic planning, direction, and tracking for completing studies within project timelinesDevelop request-for-proposals documents and solicit and evaluate bids; lead contracting process with selected CROs, collaborating with relevant departments such as Legal and FinanceManage CROs to execute clinical trials in accordance with contracted scope, costs, and timelines and within budget; actively engage with CROs on defining, monitoring and reporting on all aspects of key trial performance indicators, including country and site initiation activities, patient screening and randomization rates, and data collection activities; review and approve study documents, review and participate in the preparation of clinical documents (protocols, study reference manuals, documents to be submitted to Regulatory agencies or ethics boards, Standard Operating Procedures, guidelines and departmental policies)Prospectively identify budget, timeline, and quality risks, proactively communicate risks to management team, internal stakeholders and CRO teams, and bring team together to develop and implement risk mitigation strategies and tactics to enable trials to complete on budget, per specified timelines, and with high-quality data and deliverablesPlan and manage project finances in accordance with the Company’s strategic and operating plans and Finance policiesLead data review activities in collaboration with Data Management and other cross functional team members to ensure data quality and proactively address issues associated with the dataAssist in safety monitoring and Data Management activitiesCollaborate with the senior management team to ensure consistency across the clinical trial portfolioExperience and education requirements :
BA / BS degree or higher, preferably in the life sciencesMinimum of 10 years prior clinical trial management experience within the pharmaceutical / biotech industry or relevant clinical research organizationPrevious oncology clinical trial experience in early phase development is strongly preferredProven track record in overseeing multiple studies and in successful implementation and completion of clinical trial programsThorough knowledge of current clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical trials, clinical study design, and data management methods to ensure that the Clinical Operations remains compliant with GCP and other global regulatory guidelines or lawsPrior experience with the preparation of NDAs and MAAs and other regulatory documentsExcellent writing skills as they relate to preparation of regulatory documentsDemonstration of a broad-based and cross-functional understanding of the drug development processPay & Benefits :
The anticipated base salary for this position ranges from $180,000 to $230,000 depending on relevant skills, competencies, experience, and education. In addition, this position is eligible for target bonus, long-term-incentives, 401k retirement savings plan with company match, and a comprehensive benefits package which includes medical, dental, vision, life, and disability insurance.
EEO & Employment Eligibility :
Vividion Therapeutics, Inc. is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Privacy Policy :
The protection of your personal information is a commitment we take seriously. For information regarding our Privacy Policy (CA candidates) please visit https : / / vividion.com / publication / privacy - noticeforcalifornia -candidates / .
Salary : $180,000 - $230,000
