Clinical Pharmacology Associate - Pharmaceutical - Surrey, 1 year

Surrey  ‐ Onsite
This project has been archived and is not accepting more applications.
Browse open projects on our job board.

Keywords

Description

Clinical Pharmacology Associate - Pharmaceutical - Surrey, 1 year

  • Bachelor's degree in a scientific or health-related field.

  • Minimum of at least three years clinical research or relevant experience.

  • Strong leadership and networking skills.

  • Previous experience working in cross-functional teams or projects.

  • Strong communication skills.

  • Demonstrated problem-solving abilities.

  • Strong self-management and organizational skills.

  • First-hand experience in data management and medical writing activities and processes.

  • Demonstrated ability to work effectively cross-culturally and in a virtual work environment.

  • Strong knowledge of regulations and guidelines that apply to conduct of studies.

  • Proficiency in Excel, MS Project, risk management tools, budget monitor & control tools.

The purpose of the Associate, Clinical Pharmacology role is to provide input to the cross-functional molecule team on the clinical strategy and plan, and leads study teams of internal and external partners in the execution of studies within the clinical plan. The CPA achieves this while ensuring quality on-time and on-budget fulfilment of study deliverables. The CPA may also support non-study project assignments to transform and improve the business.

Nature of the Work:
Collaborates with colleagues in bioanalytics, biometrics, clinical development, drug metabolism and pharmacokinetics, toxicology, and regulatory affairs for the conduct and interpretation of clinical studies. Provides scientific and technical input about clinical pharmacology related issues within project teams assigned. Designing, planning and conducting controlled experiments to improve understanding of a compounds activity. Using computers, high technology measuring systems and other sophisticated equipment to collect, analyse and interpret complex data. Applying and developing the results of research to work through a variety of applications, such as new products, processes, techniques and practices. Drawing up proposals for future developmental tests. Organizing and overseeing tests of new drugs and medicines, ensuring quality control and securing approval for their use. Liaising with regulatory authorities to ensure compliance with local, national and international regulations. Interpret and integrate preclinical PK/PD information into the design, conduct and analysis of preclinical, clinical pharmacology and biopharmaceutical studies.

Start date
n.a
Duration
1 year
From
Templeton and Partners
Published at
18.07.2014
Project ID:
744090
Contract type
Freelance
To apply to this project you must log in.
Register