ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- Madrid, Spain
- Type
- Full-time
- Posted
- Jun 19, 2026
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Director, Biostatistics
at ACUTA
Job Overview
With global impact and oversight, manage a department of Biostatistics and
Statistical Programming staff ensuring that target productivity (project
allocations, utilization, and output) levels are met. May fulfill the role of
site head or functional head within a site. Manage direct personnel reports
typically consisting of Manager to Associate Director level staff from each
function. Participate in sales meetings as required and oversees departmental
proposal preparation. Monitors budget and scope of within-office projects and
takes action necessary to maximize realization. Ensure that departmental staff
contribute to intra- and interdepartmental process improvement to achieve
"best practices". Ensure that appropriate levels of professional development
and training are provided to staff. Serve as a Biostatistical resource for the
department, ensuring scientific integrity in the application of statistical
methodology to clinical trials. Provide statistical direction, technical
oversight, or consultancy on major projects or on projects involving
particularly complex statistical analyses. Represent clients at the Food and
Drug Administration (FDA) or other scientific meetings as required.
Essential Functions
• Production of High-Quality Deliverables: Ensure the high quality and
timeliness of deliverables from the Biostatistics department. Oversee and
ensures the high quality level of the Biostatistics expert review process.
Leadership: Where relevant, may include: Serve as a statistical consultant for
other members of the department and staff members from other Biostatistics
departments within the company. Maintain knowledge and awareness of
developments in Biostatistics and clinical trial methodology, and regulatory
requirements that impact analyses. Represent clients at meetings with
regulatory agencies or other regulatory meetings, may participate as a member
of a Data and Safety Monitoring Committee. May participate in independent
research activities, teaching opportunities, presentations, and preparation of
manuscripts for publication, as approved. May participate as high level lead
biostatistician on major project(s) including developing/reviewing protocols,
preparing analysis plans, and writing sections of joint clinical/statistical
reports, integrated summaries and/or new drug application (NDA) sections, as
required. Provide advanced technical expertise for internal and external
clients. Assist and contribute to governance structures where relevant.
• Management: Manage staff in accordance with organization’s policies and
applicable regulations. Responsibilities include planning, assigning, and
directing work, appraising performance and guiding professional development,
rewarding and disciplining employees, addressing employee relations issues and
resolving problems, ensure compliance with operational components (e.g.
Standard Operating Procedures (SOPs), Timesheets). Approve actions on human
resource matters. Accountable for the project level work of staff including
awareness of resource reports/strategy. Responsible for guiding leads toward
financial success at a study level.
• Compliance: Ensures compliance with strategy and initiatives. Implements
strategy and initiatives and collects feedback from the implementation (e.g.
metrics). Develop and/or provide training to staff across the business unit.
May provide feedback to draft strategy and initiatives.
• Financials: Client leaders are accountable for controlling cost and
maximizing revenue at a client/service group level. Regarding ownership of
operational components, ensure remit is in line with or maximizes business
unit needs to control costs and maximize revenue recognition. Participate in
monthly project review and operations meetings.
• Strategy and Initiatives: Defines overall strategy and initiatives for
service group or client in line with business segment owners and business unit
expectations. Contributes to global strategy and Initiative discussions with
the Senior Directors. May provide training. Owns/Project Manages defined
strategies and initiatives from the Senior Directors including delegation of
components of strategy and initiatives to Associate Directors, when it is of
when appropriate. Collaborate with other business units to develop strategies
for process improvement. Customer: Develop, maintain and expand key client
relationships. Act as Client/service group owner where significant business
unit portfolio presence exists. Own operational pieces of the business segment
(e.g. resource management for a business segment, recruitment management for a
business segment). Take responsibility for client/service group level
strategies and initiatives. Identify opportunities for additional business
from existing clients and seek to develop new clients/service offerings.
• Risk Management: Manage risks to project delivery and/or quality. Able to
manage and accountable for all study level escalations. When managing leads:
operate as an escalation point for Biostatistical team leads
• Proposals: Participate in sales meetings, as required. Contribute to
marketing materials. Create budgets, propose adjustments, and be able to
discuss budget assumptions with clients, as well as the ability to understand
and discuss pricing models. Write proposals and budgets at a study/submission
level (may have experience drafting partnership proposals). Attend project
defenses that could potentially expand the account and act as Primary Point of
Contact (POC) for New Account Defenses. Explore new business growth
opportunities and provide input into strategies that will enable Biostatistics
to capitalize on those opportunities. Take a leadership role in project
defenses that could potentially expand the account and Primary Point of
Contact (POC) for New Account Defenses. Explore new business growth
opportunities and provide input into strategies that will enable Bios to
capitalize on those opportunities.
Qualifications
• Bachelor's Degree Biostatistics or related field and 11 years relevant
experience including 4 years experience managing staff Req Or
• Master's Degree Biostatistics or related field and 11 years relevant
experience including 4 years experience managing staff Req Or
• Ph.D. Biostatistics or related field and 7 years relevant experience
including 4 years experience managing staff Req
• Typically requires 11+ years of prior relevant experience, including 4 years
experience managing staff or equivalent combination of education, training and
experience.
• Requires broad management knowledge to lead teams, and well as the ability
to influences others outside of own job area regarding policies, procedures,
and goals.
• Familiarity with most complex statistical methods that apply to Phase I-IV
clinical trials.
• In-depth knowledge of applicable clinical research regulatory requirements,
i.e., Good Clinical Practice (GCP) and International Conference on
Harmonization (ICH) guidelines.
• Excellent written and oral communication skills with excellent interpersonal
skills.
• Excellent problem solving skills.
• Excellent presentation skills.
• Excellent judgment/decision making.
• Leadership and line management skills.
• Some demonstrated success of operation within senior/executive management
teams.
• Ability to establish and maintain effective working relationships with
coworkers, managers and clients.
• Working knowledge of relevant Data Standards (such as Clinical Data
Interchange Standards Consortium (CDISC)/ADaM).
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.