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Theradex Oncology is a full-service CRO, conducting early- and late-phase oncology trials in the U.S, Europe and Asia. Theradex Oncology was founded in 1982, when we were awarded the Clinical Trials Monitoring Contract for the National Cancer Institute (NCI). We fully understand the science behind each potential cancer therapy and the challenges that come with moving therapies from mice to man. Theradex Oncology has designed and managed more than 250 early and late-phase oncology trials to date. Our mission is to assure that new discoveries in cancer drug development have the very best opportunity to be of benefit to mankind with a vision to improve treatment and make cancer a liveable disease.
What You'll Do
Theradex (Europe) Ltd. is a CRO specialising in oncology/immunology and hematology research and is focused on helping our clients bring new cancer treatments to market.
This is an excellent opportunity for the right candidate to join us to work on all aspects of the administration and documentation relating to our Phase I-III clinical trials and looking to establish a career in the pharmaceutical industry.
To apply you must at least have a Bachelor’s degree in a science discipline and having a MSc. PhD level will be an advantage. Prior relevant experience would be advantageous but is not mandatory. If you do not qualify with the required criteria, our Trainee Program may provide an opportunity within the organisation at an earlier level or provide different career pathway opportunities in other departments such as Pharmacovigilance, Data Management or Regulatory.
You will have excellent organisational and administrative skills, be enthusiastic and personable, a confident communicator and display precision and accuracy in your written work. You will assist Project Managers and Clinical Research Associates with project-related tasks in-house and occasionally at site.
Our Sponsors regularly complement us on the quality of the work we do on their behalf. That quality is no accident and you will find that we provide one of the better structured training programs in the industry as part of your induction as well as ongoing support in your role and professional development.
You will be based at our ideally located UK office in Crawley in West Sussex, close to Gatwick Airport and London, with excellent motorway and rail connections for travel when required.
Who You Are
The successful candidate will be:
- Highly Motivated
- Proactive
- Adaptable
Responsibilities
The primary responsibilities of this position include, but are not limited to, the following:
- Adhere to study-specific oversight plans.
- Support the development of study specific materials [e.g. study plans & operations manuals)
- Contribute to internal audit / corrective and preventive action (CAPA) management: contribute to the resolution of CAPA.
- Manage TMF filing of Clinical Operations documentation
- Management of study specific activities to ensure they occur per agreed timelines.
- Support management of clinical projects, to ensure issues are identified and solutions established.
- Support project meetings, arrange, take minutes, and ensure correct filing of study documents. Provide logistical and administrative support and for Theradex study team across departments including support of site visits.
- Assist the Project Manager and team in other activities, as appropriate.
- Assist new staff and provide training on electronic and other systems, as appropriate.
- Monitor and act upon study metrics.
- Maintain and ensure accuracy of information for study presented in status reports (CTMS).
What You Need
Basic Requirements
- BSc. required– preferably in a life science field or equivalent,
- MSc. PhD will be an advantage.
- Healthcare professional with at least 1 year of clinical experience, or Science Graduate with knowledge/experience in the healthcare field
- Experience of oncology clinical trials and cancer therapies preferred.
- Prior experience in a CRO/pharmaceutical environment preferred.
Preferred Requirements
- Fluent knowledge of written and verbal English
- Fluency in a second European language preferred
- Effective in writing emails/letters and varied correspondence
- Ability to set and meet personal short- and long-term goals.
- Proficient computer skills of MS Office Suite
- Able to adapt to change and work in a face paced environment.
- Strong organizational, planning, and time management skills
What we offer
We offer a friendly and supportive culture that puts people first. We provide a competitive compensation and benefits package including 6% pension contribution, private medical insurance, sick pay and income protection insurance, life assurance and eyecare voucher scheme.
This job does not offer company sponsorship
Theradex is an equal opportunity employer. All qualified applicants are encouraged to apply and will receive consideration for employment.
