My client is looking for a Director Business Development and a Business Development Manager to join their global sales team. The right candidate will need to come from a recruitment background as you will be selling my clients staffing solutions throughout Europe.
A CRA II role has come up with a midsized German CRO. A Clinical Research Associate / CRA with at least 2 years previous monitoring experience, looking for a new challenge will be rewarded with a unique chance at a midsized European CRO. New career development opportunities, office-based option.
JOB TITLE CRA II / Clinical Research Associate II in Kiel
LOCATION Kiel / Germany / office based / Central Europe / Schleswig-Holstein /DACH AREA
A Senior Clinical Research Associate (Senior CRA) role has come up with a midsized CRO. A Clinical Research Associate / SCRA with more than 3 years previous monitoring experience, looking for a new challenge will be rewarded with a unique chance at a CRO with a good working environment. New career development opportunities, home or office-based options.
JOB TITLE Senior Clinical Research Associate / Senior CRA / Senior Clinical Research Associate
Manager/Senior Medical Writer - W.London / Middlesex / Bucks / Berks An exciting opportunity to join a fast paced and dynamic team in one of the leading CROs in the world. The Senior Medical Writer researches, creates and edits all documents relating to clinical trials. You will be the primary contact for medical writing projects, setting timelines, providing leadership and running training to support more junior writing staff.
Regulatory Affairs Specialist - Medical Devices - United Kingdom
This company is a leader in medical device manufacturing and specialises within the orthopaedics market. The company operates in more than 90 countries, with over 7000 employees and generates billions of dollars in sales. With a very successful history, this company looks to always improve and adapt to increase innovation and quality.
A global CRO, specialising in all major therapeutic areas, is looking to recruit a talented Medical Writer to work within Clinical Research Services - specifically phase II. This is a home based position; you will become an integrated member of a well-established team, responsible for producing high quality regulatory documents. You will be rewarded with a highly competitive salary, and excellent opportunities to progress your career, and your own personal development.
Our client is a growing pharmaceutical company with therapy franchises in oncology and cardiovascular medicine. The European team is becoming increasingly busy and as a result, the company is seeking a Quality Assurance Manager to manage the functions of a fully functional GCP/GLP Quality Assurance program that will assure all global studies (Phase I through III) can withstand regulatory scrutiny from all regulatory bodies.
A Clinical Study Manager is required for a leading global CRO, to coordinate clinical operations and the activities of project teams. Ideal for candidates looking for career progression within an award winning and reputable company. The position is permanent, home-based and full- time.
i-Pharm Consulting are seeking on behalf of a leading CRO a FREELANCE CRA to work on an initial 6 month contract. This is a home-based role covering monitoring of sites in the North-West of the UK. These are sites in Birmingham, Nottingham, Derby, Leicester.
Our client is a world leader in the pioneer of clinical research and works on behalf of a large number of global pharmaceutical companies.
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