Alnylam Pharmaceuticals
Associate Director Clinical Operations
Alnylam Pharmaceuticals, Cambridge, Massachusetts, us, 02140
Associate Director Clinical Operations
Alnylam Pharmaceuticals
Overview
The Associate Director is responsible for leading a team of Global Trial Leaders and Trial Managers within the Study Management Organization. The position is responsible for staff development and study oversight, and will work closely with the Director for input on project assignments, workload distribution, resourcing, and prioritization. The Associate Director directly influences trial objectives and ensures common operational issues/challenges are identified within and potentially across trials and programs and are addressed through operational risk mitigation, including proposals for alternative solutions. The Associate Director is also accountable for the operational execution of all trials within a program.
Summary of Key Responsibilities
Define the Operational Strategy for each trial in the program and gain governance endorsement on proposed plans.
Lead operational scenario planning and mitigate trial-level risks that may impact timelines or budget.
Ensure appropriate timely and quality oversight, and appropriately escalated issues to the Director, Quality and functional leadership.
Communicate the operational strategy, and defend the operational plan and costs associated to CTWG, CDST, Director, leadership and at governance meetings as appropriate.
Lead and ensure inspection readiness for the trial/s.
Build a knowledgeable and skilled team with competencies and capabilities to successfully set up and deliver clinical trials.
Promote strong collaboration across cross-functional teams.
Set goals in alignment with company, program, and departmental goals.
Ensure staff training on procedures and systems associated with their roles.
Develop a team that consistently achieves strong results through nurturing individual growth, effectively managing performance, and providing guidance.
For early development programs, AD may represent Clinical Operations at CDST.
Interface with internal key stakeholders including Finance, Program Management, Vendor Management, Safety, Accounting, Supply, Quality Assurance, Data Management, Statistics, Clinical Research, Commercial, Regulatory, Bio Analytical, Medical Affairs; and act as a liaison between groups.
Lead or participate in process improvement activities at a trial and department level as needed.
Participate in preparation for, and conduct of, Health Authority Inspections and internal QA audits.
Travel as expected (average annual 10% but flexible to exceed or fall below as required).
Qualifications
BS/BA degree is required.
Minimum 8+ years of clinical research experience gained with a CRO, Biotech, or Pharmaceutical Company working on Phase 1-4 global clinical trials.
3-5 years leading end-to-end global clinical trials with experience in conducting Phase 3 registrational trials.
Experience in and knowledge of the pharmaceutical development process.
Excellent decision-making, analytical and strong financial management skills are essential to this position.
Ability to manage all aspects of execution of a clinical trial.
Must possess excellent leadership skills, proven ability to foster team productivity and cohesiveness, and the ability to operate and execute with limited supervision.
Experience in leading without authority and in multifaceted matrixed and global environments.
Strong project planning/management, communication (written and verbal) and presentation skills.
Minimum 2+ years prior line management experience or 3+ years matrixed leadership experience required.
Exceptional organizational skills and ability to deal with competing priorities, also strong reasoning and problem-solving ability.
Apply project management best practices to programs. Experience in novel clinical drug development.
Proficient with MS Office Suite (Excel, Word, PowerPoint) and MS Project.
Seniority level
Director
Employment type
Full-time
Job function
Project Management
Industry
Pharmaceutical Manufacturing
Location: Cambridge, MA
Compensation range: $260,000.00–$360,000.00
For full details, see the original job posting.
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Overview
The Associate Director is responsible for leading a team of Global Trial Leaders and Trial Managers within the Study Management Organization. The position is responsible for staff development and study oversight, and will work closely with the Director for input on project assignments, workload distribution, resourcing, and prioritization. The Associate Director directly influences trial objectives and ensures common operational issues/challenges are identified within and potentially across trials and programs and are addressed through operational risk mitigation, including proposals for alternative solutions. The Associate Director is also accountable for the operational execution of all trials within a program.
Summary of Key Responsibilities
Define the Operational Strategy for each trial in the program and gain governance endorsement on proposed plans.
Lead operational scenario planning and mitigate trial-level risks that may impact timelines or budget.
Ensure appropriate timely and quality oversight, and appropriately escalated issues to the Director, Quality and functional leadership.
Communicate the operational strategy, and defend the operational plan and costs associated to CTWG, CDST, Director, leadership and at governance meetings as appropriate.
Lead and ensure inspection readiness for the trial/s.
Build a knowledgeable and skilled team with competencies and capabilities to successfully set up and deliver clinical trials.
Promote strong collaboration across cross-functional teams.
Set goals in alignment with company, program, and departmental goals.
Ensure staff training on procedures and systems associated with their roles.
Develop a team that consistently achieves strong results through nurturing individual growth, effectively managing performance, and providing guidance.
For early development programs, AD may represent Clinical Operations at CDST.
Interface with internal key stakeholders including Finance, Program Management, Vendor Management, Safety, Accounting, Supply, Quality Assurance, Data Management, Statistics, Clinical Research, Commercial, Regulatory, Bio Analytical, Medical Affairs; and act as a liaison between groups.
Lead or participate in process improvement activities at a trial and department level as needed.
Participate in preparation for, and conduct of, Health Authority Inspections and internal QA audits.
Travel as expected (average annual 10% but flexible to exceed or fall below as required).
Qualifications
BS/BA degree is required.
Minimum 8+ years of clinical research experience gained with a CRO, Biotech, or Pharmaceutical Company working on Phase 1-4 global clinical trials.
3-5 years leading end-to-end global clinical trials with experience in conducting Phase 3 registrational trials.
Experience in and knowledge of the pharmaceutical development process.
Excellent decision-making, analytical and strong financial management skills are essential to this position.
Ability to manage all aspects of execution of a clinical trial.
Must possess excellent leadership skills, proven ability to foster team productivity and cohesiveness, and the ability to operate and execute with limited supervision.
Experience in leading without authority and in multifaceted matrixed and global environments.
Strong project planning/management, communication (written and verbal) and presentation skills.
Minimum 2+ years prior line management experience or 3+ years matrixed leadership experience required.
Exceptional organizational skills and ability to deal with competing priorities, also strong reasoning and problem-solving ability.
Apply project management best practices to programs. Experience in novel clinical drug development.
Proficient with MS Office Suite (Excel, Word, PowerPoint) and MS Project.
Seniority level
Director
Employment type
Full-time
Job function
Project Management
Industry
Pharmaceutical Manufacturing
Location: Cambridge, MA
Compensation range: $260,000.00–$360,000.00
For full details, see the original job posting.
#J-18808-Ljbffr