If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to
transform the lives of patients and their families.
We are dedicated to developing
life-changing medicines for people with serious diseases — often with limited or no
therapeutic options.
We have a diverse portfolio of marketed medicines, including leading
therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments.
Our patient-focused and science-driven approach powers pioneering research and development
advancements across our robust pipeline of innovative therapeutics in oncology and
neuroscience.
Jazz is headquartered in Dublin, Ireland with research and development
laboratories, manufacturing facilities and employees in multiple countries committed to
serving patients worldwide.
Please visit
www.jazzpharmaceuticals.com
for more information.
Brief Description
The Business & Technology Capabilities (B&TC) Sr.
Analyst works closely with B&TC and GCDO colleagues, in collaboration with Information Services (IS) to support cross functional clinical study teams regarding the implementation and management of digital systems/technology used by GCDO including but not limited to Veeva Clinical Vault.
The B&TC Sr.
Analyst demonstrates a good understanding of Veeva Clinical Vault functionality.
The B&TC Sr.
Analyst works with the 'Performance and Training' function to facilitate the collation, visualization, analysis & storage of relevant metrics for GCDO to ensure optimal trial performance and aid continuous improvement
Essential Functions/Responsibilities
Establishes and maintains, digital systems on behalf of GCDO primarily the Veeva Clinical Vault applications e TMF, CTMS, SSU and Site Connect, plus other Clinical Systems as required
Carry out required activities in JV e TMF for all Clinical Vault/e TMF user access requests in accordance with the documented process
Carry out required system maintenance in JV e TMF to ensure end users can perform their role in accordance with the documented process
Works closely with Business owners and system owners of digital system including but not limited to Veeva Clinical Vault, to ensure GCDO teams are trained appropriately in the functionality of relevant digital systems
Collaborates with other functional areas/departments and key stakeholders to maximize the utilization of the digital systems (e.g.
creating dashboards, reports, ensuring best use of all Clinical Vault functionality
Collaborates with partner vendors, as needed, in relation to system knowledge sharing and utilization
Collaborates with subject matter experts on development of relevant digital system training materials, QMS documentation, and Validation activities and documentation
Maintains a sound familiarity with Jazz's systems and related processes
Establishes and maintains, digital systems on behalf of GCDO primarily the Veeva Clinical Vault applications e TMF, CTMS, SSU and Site Connect, plus other Clinical Systems as required
Carry out required activities in JV e TMF for all Clinical Vault/e TMF user access requests in accordance with the documented process
Carry out required system maintenance in JV e TMF to ensure end users can perform their role in accordance with the documented process
Works closely with Business owners and system owners of digital system including but not limited to Veeva Clinical Vault, to ensure GCDO teams are trained appropriately in the functionality of relevant digital systems
Collaborates with other functional areas/departments and key stakeholders to maximize the utilization of the digital systems (e.g.
creating dashboards, reports, ensuring best use of all Clinical Vault functionality
Collaborates with partner vendors, as needed, in relation to system knowledge sharing and utilization
Collaborates with subject matter experts on development of relevant digital system training materials, QMS documentation, and Validation activities and documentation
Maintains a sound familiarity with Jazz's systems and related processes
Identifies improvement opportunities related to digital systems, and assists with developing enhancement plans and roadmaps
Organizes and delivers relevant specialist training sessions and workshops with a key focus on digital systems
Required Knowledge, Skills, and Abilities IT-literate and passionate/experienced towards new technology and digital systems including, but not limited to Microsoft-based applications and Veeva Clinical Vault applications CTMS, e TMF, SSU and Site Connect
An experienced clinical trials professional who is well versed in the field of clinical study management activities, combined with excellent project management, training & mentoring capabilities
Previous experience working in Veeva Clinical Vault as an end user, business, or system administrator
Ability to effectively interface with CROs and software vendor
Previous experience working in clinical trials, with emphasis on Gx P and compliance
Has a sound working knowledge of clinical operations, clinical processes, Trial Master File regulations medical terminology, global CROs and vendor management
Excellent interpersonal and communication skills, both written and verbal
Good time management and organizational skills
Quality driven with a focus on attention to detail
Ability to work independently and take initiative
Flexible approach with respect to work assignments and new learning
Ability to prioritize workload and manage multiple and varied tasks with enthusiasm
Ability to work effectively in a matrix environment and to demonstrate, and foster, teamwork within the group, as well as across the organization
Required/Preferred Education and Licenses A minimum of a BA/BS, preferably in the scientific/healthcare and/or technology field
A minimum of 5 years of experience in clinical related technology for the pharmaceutical/biotechnology industry
Knowledge of FDA/ICH guidelines and industry standard practices regarding the management of clinical trial data and studies.
Working knowledge of FDA Guidance Documents: Computerized Systems Used in Clinical Trials, General Principles of Software Validation.
Working knowledge of 21 C.
F.
R.
Part 11 Jazz Pharmaceuticals is an equal opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
FOR US BASED CANDIDATES ONLY
Jazz Pharmaceuticals, Inc.
is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive.
For this role, the full and complete base pay range is: $100,000.00 - $150,000.00
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors.
The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy.
Internal equity considerations will also influence individual base pay decisions.
This range will be reviewed on a regular basis.
At Jazz, your base pay is only one part of your total compensation package.
The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation.
For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html .