FULL REMOTE - CLINICAL TRIALS - Principal TA Methodology Statistician - $160,000 to $200,000

REMOTE, REMOTE · $160,000 to $200,000

OPEN JOB: Principal / Senior Principal TA Methodology Statistician (HTA and Market Access)
LOCATION: Job is fully remote
SALARY: $160,000 to $200,000
BONUS ELIGIBLE - Yes
FULL-TIME
FULL BENEFITS
INDUSTRY: Pharmaceutical / Biotech
JOB CATEGORY: Medical / Health - Healthcare IT

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

Description

Biostatistics and Data Sciences (BDS) is a global organization within the Human Pharma Business Unit. Working in close collaboration with other functions at the company and external vendors we combine methodological and technical data science skills with business and scientific expertise to drive smart, timely and confident decision making at every stage of drug development, approval, and access.
On our journey to transform BDS into a modern data science organization our intent is to create a learning organization in which people develop and deploy leading-edge data science approaches and technologies to actively plan, generate and evaluate evidence that shapes informed decision-making along the value chain.
Join our function Therapeutic Area and Methodology (TAM) Statistics and become part of our global methodology group. Drive user-centric innovations to foster holistic evidence implementation and their accessibility to our business by providing consultancy and solutions to our clinical development teams.

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.

Requirements
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)

If you are interested in pursuing this opportunity, please respond back and include the following:

MS WORD Resume
required compensation.
Contact information.
Availability

Upon receipt, one of our managers will contact you to discuss the position in full detail.

JASON DENMARK
Recruiting Manager
INTERMEDIA GROUP, INC.
EMAIL: jdenmark@intermediagroup.com
LINKEDIN: https://www.linkedin.com/in/jasondenmark/

FULL REMOTE - CLINICAL TRIALS - Principal TA Methodology Statistician - $160,000 to $200,000

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