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Principal / Senior Principal TA Methodology Statistician (HTA and Market Access)

Key Facts

Remote From: 
Category:  Statistician
Full time
Senior (5-10 years)
English

Roles & Responsibilities

  • Master of Science (MSc) or Doctoral Degree (PhD) in Statistics or Mathematics or related field
  • At least five (5) years of experience for Principal and seven (7) years for Senior Principal
  • Solid knowledge/learning abilities on statistical methodology
  • HTA knowledge related to global reimbursement process

Requirements:

  • Collaborate with statisticians and provide statistical-methodological expertise
  • Integrate external data into clinical development and HTA reports
  • Evaluate advanced statistical methods to foster holistic evidence generation
  • Provide statistical-methodological trainings to statisticians and non-statisticians

Job description

Principal / Senior Principal TA Methodology Statistician (HTA and Market Access)

Remote

Full Time

Ideal Candidate
Experience with clinical trial development, not just at the trial level but the overall asset development process.

Solid knowledge/learning abilities on statistical methodology

Focus on talent with a pharma background as being the ideal

HTA - health technology assessment knowledge - this is related to global reimbursement process

Market Access knowledge

Duties & Responsibilities

In your new role, you will closely collaborate with other statisticians and provide statistical-methodological expertise on multiple of the following topics:

integration of external data into clinical development and HTA reports, e.g. via usage of Bayesian borrowing and external control

complex evidence synthesis including Bayesian network meta-analysis

patient-focused drug development including clinical endpoint development and psychometric validation of instruments

clinical trial design that enables RCT generalizability to real world populations and settings, for example, pragmatic trial and flexible augmented clinical trial for improved evidence generation (FACTIVE)

target trial emulation, causal inference and real world evidence methodology

You will evaluate advanced statistical methods to foster holistic evidence generation by prototyping and developing ready-to-use toolkits. you will drive their implementation.

You will contribute to the large-scale implementation for such innovation toolkits.

You will provide pragmatic solutions to our clinical development teams to foster holistic evidence generation that accompanies needs for different stakeholders including internal decision making, regulatory, market access and medical affairs.

You will present and quantitively illustrate the application of complex statistical concepts to stakeholders like management, external partners, and/or regulatory agencies.

Furthermore, you will provide statistical-methodological trainings to statisticians and non-statisticians.

Additionally, you will mentor and guide other colleagues. You will define and supervise the technical and scientific work of interns and students and contribute to their professional journey.

Principal Requirements:

Master of Science (MSc) or Doctoral Degree (PhD) from an accredited institution, in Statistics or Mathematics or related field (Psychology, Data Science, Finance, etc.).

At least five (5) years of experience as a statistician or data scientist in an area relevant for the specific role

Senior Principal Requirements:

Master of Science (MSc) or Doctoral Degree (PhD) from an accredited institution, in Statistics or Mathematics or related field (Psychology, Data Science, Finance, etc.).

At least seven (7) years of experience as a statistician or data scientist in an area relevant for the specific role.

Additional Requirements:

Working experience might be partially compensated by broad and deep topic-specific knowledge, e.g. with respect to statistical methodology.

Statistical experience gained in an international context and ideally in different companies/ academic institutions.

Ideally, additional qualification and experience in a leadership role.

In-depth knowledge of competitor and agency strategies and/or in-depth knowledge regarding statistical approaches developed and implemented by other companies or academia in a global context.

In-depth knowledge of parts of BDS and related parts of other organizations at BI regarding their contribution to BIs strategy.

In-depth knowledge of statistical methodology and clinical development.

In-depth understanding of statistical concepts related to clinical development.

Ability to supervise scientific/technical work.

Proficient in the use of software languages to implement statistical concepts.

Mindful of local, global, internal and external cultures to ensure that messages are received positively and effectively.

Ability to lead and facilitate meetings required.

Evidence of strong teamwork, ideally also in global and remote context.

Very good interpersonal skills with the ability to interact effectively with people, internally and externally (e.g., CROs, experts, management).

Ability to pro-actively identify issues and solutions and to interact with internal and external bodies on statistical topics.

Language skills: English: fluent (Read/Write/Speak).

Know, understand, and implement:

International regulations and guidelines for good clinical and statistical practice from all ICH regions

The various international guidelines on clinical development, data standardization, and

BI processes and SOPs that govern clinical development in particular with respect to strategic areas e.g. Clinical Development Plan)

Skills and Certifications

Statistical Methodology
Clinical Development

Screening Questions – Explain in detail for below questions.

Full Name:

Master of Science (MSc) or Doctoral Degree (PhD) from an accredited institution, in Statistics or Mathematics or related field (Psychology, Data Science, Finance, etc.)?

Total experience as Principal / Senior Principal TA Methodology Statistician (HTA and Market Access)?

At least five (5) years of experience as a statistician or data scientist in an area relevant for the specific role?

What has been your exposure to the clinical development process?

What have you been responsible for contributing to the process?

Experience with clinical trial development, not just at the trial level but the overall asset development process?

Solid knowledge/learning abilities on statistical methodology ?

Focus on talent with a pharma background as being the ideal?

HTA - health technology assessment knowledge - this is related to global reimbursement process?

Market Access knowledge?

Statistical Methodology?

Clinical Development?

Contact Number:

E mail Id:

LinkedIn Id:

Full Address (Street, City, States, Zip Code Required)

Notice period: (in weeks):

Current work authorization status:

Expected Salary?

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