Unser Klient ist einer der 10 grĂ¶Ăźten CROs in Deutschland und ist Momentan auf der Suche nach Projektleitern mit starker Erfahrung, die so bald wie mĂ¶glich Ihrer Firma beitreten kĂ¶nnen. LĂ¤ngere KĂĽndigungsfristen werden fĂĽr die idealen Kandidaten auch in betracht genommen.
Clinical Project Manager. Are you looking for an exciting opportunity to join a recognised company who are going through an overwhelming period of growth? A leading pharmaceutical company in Oxfordshire are seeking a committed and proactive individual to join their team as a Clinical Project Manager operating in their Medicines Development and Medical Affairs functional area.
My client is a Global Top 5 CRO, looking to recruit a Senior Director to manage an assigned portfolio of clients. You will be working within Phase II and III and ideally have Senior Director experience in a CRO or Pharma environment. You will be required to maintain strong client relationships and drive repeat business.
An excellent opportunity has arisen for a Regulatory Affairs Manager, Medical Devices to join a global technology-driven multi-speciality healthcare company focused on discovering, developing and commercialising innovative products for the eye care, neuromodulator, skin care and other specialty markets. With specialty product lines focused on high-growth markets, the company represents a new multi-specialty health care model for the future.
Fantastic opportunity for a senior Regulatory Affairs Manager looking to provide regulatory support for oncology products where you will plan, manage and execute regulatory activities within European territories as required. Working on assigned oncology project or projects (either investigational or marketed products) you may also be required to provide support to Director, Regulatory Affairsâ€“ Oncology.
Fantastic opportunity for an experienced Clinical Project Manager to join a high performance team within global pharma. You will aid the cross-functional study team in managing one or more clinical studies globally or within specified regions within the Neuroscience & General Medicine PCU, ensuring that study milestones and deliverables are achieved according to agreed quality standards & timelines & that quality of data are acceptable and suitable for reg submission.
Our client, a top global pharma company is looking for talented regulatory affairs professional. This role will be based at their award winning Development site and take lead EU regulatory responsibility for an exciting Oncology development candidate with multiple indications. /b>
Study Management Associate - Pharma - UK (office based) - contract
Study Management Associate required for a world leading Pharmaceutical company to join their operations on a 12 month contract. Your background should consist of previously working as a CRA and if you have been involved in trial coordination it would be useful as well.
This role is office-based at their operations at Uxbridge. Excellent day rate on offer. ...
JOB ROLE The Regulatory Affairs Manager will manage all aspects of regulatory submissions (preparation, submission and approval) for Class III Medical Devices in Europe, Africa and Middle East. You will provide regulatory input and guidance to project and regulatory teams by keeping up to date with latest medical device regulations.
Opportunity for an experienced Senior CRA / Lead CRA to join this Global Pharma organisation based to the West of London. There is emphasis on clinical study implementation oversight including study monitoring, compliance and youâ€™ll supervise CRA/CTA (TMF) activities provided by external partners. Youâ€™ll co-monitor across a range of clinical studies (Phase I-IV) and support Clinical Project Managers in the overall management of global trials.
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