Drug development processes jobs

Senior Clinical Research Associate I/II - FSP - Sydney or Melbourne

Fortrea · Posted Nov 11, 2026

Open

Sydney, New South Wales, Australia +1 more
Senior
3+ years

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Senior Clinical Research Associate I/II - FSP - Sydney or Melbourne

Fortrea · Posted Nov 11, 2026

Open

Sydney, New South Wales, Australia +1 more
Senior
3+ years

Apply with Referso

Senior Manager, Medical Science Liaison, France

Revolution Medicines · Posted Nov 11, 2026

Open

Paris, Île-de-France, France
Manager
8+ years

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Lead field medical activities within an assigned French territory, engaging KOLs, supporting medical education, and providing scientific insights to internal teams.

Responsibilities

Execute approved field medical plans within an assigned French territory
Engage in peer-to-peer scientific dialogue with healthcare professionals
Serve as therapeutic expert and thought partner to internal teams
Liaise between Revolution Medicines and clinical study sites/investigators
Provide support for medical education, advisory boards, and medical congresses

Requirements

Doctoral degree in scientific or medical discipline
Nice to have: Experience in lung and gastrointestinal cancers

Skills

Relationship building with KOLs Scientific presentation Clinical data communication Scientific insight synthesis Cross-functional collaboration Knowledge of clinical research methodologies

Global Product Leader

AstraZeneca · Posted Nov 9, 2026

Open

Boston, Massachusetts, United States +1 more
Hybrid
Full-time · Senior
$252K–$377K per year
5+ years

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A senior leadership role leading a cross-functional Global Product Team to design and deliver a successful strategy for a respiratory asset through the brand's entire life cycle.

Locations (2)

Boston, Massachusetts, United States
Gaithersburg, Maryland, United States

Compensation

The annual base salary for this position ranges from $251,610–377,415.

Responsibilities

Define and drive the strategic and scientific value creation of the brand
Manage the development path, governance approval, growth, and maturity of the brand (Life Cycle Management)
Engage and consult with KEEs to establish and nurture effective partnerships and networks
Build and effectively lead high-performing cross-functional teams
Ensure disease strategy is innovative with a balanced focus on safety, efficacy, and market access

Requirements

Masters Degree
Nice to have: PhD

Global Product Leader

AstraZeneca · Posted Nov 9, 2026

Open

Boston, Massachusetts, United States +1 more
Hybrid
Full-time · Director
$252K–$377K per year
5+ years

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Senior leadership role for a Global Product Leader in Respiratory, leading a cross-functional Global Product Team to design and deliver a successful global brand strategy through the brand's life cycle.

Locations (2)

Boston, Massachusetts, United States
Gaithersburg, Maryland, United States

Compensation

The annual base salary for this position ranges from $251,610–377,415. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program.

Responsibilities

Define and drive the strategic and scientific value creation of the brand
Manage development path, governance approval, growth and maturity of the brand (Life Cycle Management)
Integrate diverse internal and external perspectives into the process
Engage and consult with KEEs to establish and nurture effective partnerships and networks
Build and effectively lead high performing cross-functional teams

Senior Regulatory Affairs Director- Infectious Diseases

AstraZeneca · Posted Nov 5, 2026

Open

Gaithersburg, Maryland, United States
Full-time · Senior
$218K–$327K per year
10+ years

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Lead the global regulatory strategy for complex products, securing rapid approval and guiding high-profile development programs across therapeutic areas.

Compensation

The annual base salary for this position ranges from $218,058.40 - $327,087.60 USD Annual. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles) or to receive a retirement contribution (hourly roles).

Responsibilities

Effectively lead or deputise for Therapeutic Area (TA) VP/Regional VP in senior-level interactions internally or externally, including contributions to internal governance
Develop and implement regulatory strategies for products, ensuring rapid approval with advantageous labeling
Lead the planning and construction of global dossiers and core prescribing information
Conduct regulatory risk planning and mitigation
Serve as the single point of contact and Global Regulatory Affairs representative on Product Development Teams

Requirements

Master's degree in a science-related field
Nice to have: experience in Infectious Diseases
Nice to have: FDA advisory committee meetings
Nice to have: Oral explanations
Nice to have: Scientific Advice

Skills

regulatory strategy

Safety Surveillance Principal Specialist

Novo Nordisk A/S · Posted Nov 8, 2026

Open

Søborg, Capital Region, Denmark
Senior
DKK 847K–DKK 1M per year

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Lead the safety surveillance strategy for responses to Health Authority questions across Novo’s incretin portfolio, mainly within diabetes and obesity treatment.

Compensation

Salary: For this role, the Annual Base Salary ranges from 847,000.00 to 1,245,100.00 DKK, corresponding to the level of the position.

Responsibilities

Lead high‑impact activities across the incretin portfolio
Act as the safety surveillance lead for strategic, scientific responses to safety Q&A from all Health Authority interactions
Maintain overview of activities, including studies, submissions and questions and answers from Health Authorities
Represent Safety Surveillance in Health Authority meetings
Maintain overview of safety contributions to study reports, regulatory submissions, protocols and other key documents

Requirements

Master’s degree in Life Sciences (e.g. Pharmacy, Medicine, Veterinary Medicine or Biology)

Skills

drug safety pharmacovigilance drug development processes global regulatory requirements

Manager

Boehringer Ingelheim · Posted Nov 4, 2026

Open

Shinagawa, Japan

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Clinical Data Scientist

Responsibilities

Lead and/or support statistical analyses, data transformation, interpretation, and reporting for Phase I-IV clinical trials.
Contribute to the analysis of clinical registries, observational studies, and real-world data sources.
Develop and implement data science solutions to support drug development, regulatory submissions, and evidence generation.
Collaborate with cross-functional stakeholders including Clinical Development, Regulatory Affairs, Pharmacovigilance, Medical Affairs, and Global Development teams.
Ensure statistical deliverables are scientifically sound, regulatory compliant, and delivered according to timelines.

Requirements

Bachelor's in Statistics
Master's in Statistics
PhD in Statistics
Bachelor's in Mathematics
Master's in Mathematics

Skills

clinical data science biostatistics clinical trial analytics statistical programming analytical tools global cross-functional development clinical trial methodology statistical principles drug development processes

See full job description

Senior Regulatory Affairs Director- Infectious Diseases

AstraZeneca · Posted Nov 5, 2026

Open

Gaithersburg, Maryland, United States
Hybrid
Full-time · Director
$218K–$327K per year
10+ years

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The Senior Regulatory Affairs Director (SRAD) leads the global regulatory strategy for complex products to secure rapid approval that meets business, market, and patient needs.

Compensation

The annual base salary for this position ranges from $218,058.40 - $327,087.60 USD Annual.

Responsibilities

Effectively lead or deputise for Therapeutic Area (TA) VP/Regional VP in senior-level interactions internally or externally
Develop and implement regulatory strategies for products, ensuring rapid approval with advantageous labeling
Lead the planning and construction of global dossiers and core prescribing information
Conduct regulatory risk planning and mitigation
Serve as the single point of contact and Global Regulatory Affairs representative on Product Development Teams

Requirements

Master’s degree in a science-related field
Nice to have: Infectious Diseases
Nice to have: Advanced degree

Skills

global regulatory science drug development processes Major Health Authority interactions FDA advisory committee meetings

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