Lead Project Data Manager
SEC Pharma is working closely with a world leading service provider to the Pharmaceutical industry in the search for a Project Clinical Data Manager. This company provides a full service of CRO activities to the majority of the big Pharma and Biotech's. You will be working at a company renowned for their exceptional service delivery and repeat business. Not only this, they also provide the best training of any CRO in the industry and they are able to offer a great salary as well as a generous benefits and bonus package.
This role has two main functions: Project Management and DM operational expertise.
You will be the main point of contact for the study sponsor for your studies. You will have a support network of other DMs who you will delegate work too. You will be a subject matter expert in Study set-up, leading studies, communication of timelines to internal and external stakeholders and you will be responsible for data quality and metrics. You will be an adept EDC user across the major EDC platforms. Phase I-IV experience is preferred as well as specific TA experience including Oncology, CVS or Neurology. If you have some experience working on Biotech company trials this would also be great.
To be considered for interview I would suggest you have a CRO background with experience leading multiple studies at once. If you are home based you will need to be self-sufficient. This role will be autonomous and although you will have support, you will be expected to very self-proficient in the running of your projects.
The key duties;
- Primary point of contact for customer/Sponsor
- Oversight lead of all CDM deliverables
- Establish strong communication channels with internal and external stake holders
- Drive and motivate key personnel within your teams
A full job description is available on request