Latest Clinical Research Associate Jobs

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight and clinical development for oncology and hematology programs, with responsibilities spanning study design, safety monitoring, data interpretation, and regulatory engagement. The Medical Director will collaborate with cross-functional teams and external experts to ensure clinical integrity and patient-centered decision-making in late-stage drug development. The position requires deep expertise in hematology-oncology and experience in Phase I–III trials within a pharmaceutical or biotech setting.

GSK PLN 455,250 – PLN 758,750 pa

Medical Director, Oncology Clinical Development - Hematology

Serves as the physician lead within the oncology clinical development team, providing medical expertise to design, conduct, and interpret clinical studies in hematology oncology. Responsible for medical monitoring, safety oversight, protocol development, and cross-functional collaboration to ensure patient safety and clinical integrity. Engages with investigators and regulatory bodies, contributing to regulatory submissions and scientific communications.

GSK

Global Labelling Associate Director, Content (Established Products)

Leads the development and maintenance of global labelling strategies and core documents for pharmaceutical products, ensuring scientific accuracy and regulatory compliance. Facilitates cross-functional alignment, supports health authority interactions, and mentors team members. Focuses on consistent, competitive product information across global markets.

Novartis

Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves leading the development and maintenance of global labelling strategies and core documents for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will work cross-functionally to align labelling content, interpret clinical data, and ensure compliance with global regulatory standards. Key responsibilities include supporting health authority interactions, mentoring team members, and maintaining scientific accuracy across product lifecycles.

Novartis London, United Kingdom

Hybrid Permanent

Senior Executive Assistant to CEO

Provide high-level executive support to the CEO of a clinical-stage TechBio company, managing a complex calendar, international travel, and communications while serving as a key liaison across global teams and stakeholders. Enable strategic priorities through proactive coordination of board meetings, investor events, and cross-functional initiatives in a fast-paced biotechnology environment. Operate with discretion and precision in a mission-driven organization focused on accelerating drug discovery through AI and industrialized biology.

Recursion North Tyneside, NE29 8EP, United Kingdom US$130,460 – US$164,780 pa

On-site Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads global labelling strategy and governance for oncology products, managing a team of professionals and ensuring compliance with regulatory standards. Works cross-functionally across R&D, Regulatory, Safety, and Commercial to shape clear, patient-focused product labels. Engages with regulatory authorities and drives innovation in labelling policy and practice.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and governing oncology product labelling across the R&D lifecycle. Ensures regulatory compliance, shapes patient-focused labelling strategies, and collaborates with cross-functional stakeholders including Regulatory, Safety, and Commercial. Engages with health authorities to advance innovative labelling approaches in oncology.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labelling across the drug lifecycle, ensuring regulatory compliance and alignment with patient needs. Works cross-functionally with R&D, Regulatory, Safety, and Commercial to shape strategic labelling policies and engage with health authorities. Focuses on creating clear, compliant, and patient-centric product information in a highly regulated environment.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global labelling team for oncology products, shaping clear, compliant, and patient-focused product labels. Interfaces with regulatory authorities and cross-functional stakeholders to drive labelling strategy and governance. Focuses on aligning regulatory, scientific, and commercial objectives across the oncology portfolio.

GSK

Hybrid Permanent

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

Leads medical writing for complex clinical and regulatory projects, including protocols, study reports, and submission dossiers. Translates clinical data into clear scientific narratives and acts as a subject matter expert on regulatory standards. Works cross-functionally in a fast-paced, mission-driven HIV-focused environment.

GSK

On-site Permanent

Senior Director, Translational Genetics

Lead a team of translational genetics scientists to drive data-driven insights across GSK's drug development pipeline, integrating genetic, genomic, and clinical data to inform target validation, biomarker discovery, and patient stratification. Work within cross-functional teams to address key translational questions in therapeutic areas such as respiratory, immunology, and neurodegeneration. Foster innovation through internal collaboration and external academic partnerships while advancing methodological development in statistical genetics.

GSK Stevenage, United Kingdom US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic, and clinical data in support of drug discovery and development. Focuses on generating disease-relevant insights across therapeutic areas such as respiratory, immunology, neurodegeneration, and hepatology. Drives innovative analytical approaches and external collaborations to address key translational questions and advance GSK’s pipeline.

GSK Canterbury, United Kingdom US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic, and clinical data in support of drug discovery and development. Focuses on addressing key translational questions using statistical genetics and innovative analytical approaches across therapeutic areas such as respiratory, immunology, and neurodegeneration. Works within cross-functional teams and establishes external collaborations to advance GSK's R&D pipeline.

GSK

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to drive data-driven insights supporting drug discovery and development across key therapeutic areas. Applies advanced statistical genetics and integrates genomics and clinical data to address translational questions. Fosters innovation, external collaborations, and scientific leadership within a multidisciplinary environment.

GSK US$207,075 – US$345,125 pa

Hybrid Permanent