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Senior Clinical Project Manager - Geneva Description PURPOSE OF THE ROLE To drive and manage... as the Clinical Trial Leader (CTL) or Clinical Research Manager (CRM). The Senior Clinical Project Manager (SCPM... decisions, Lead and coordinate investigator/site selection and manage/present at Investigator Meetings
Contract: Permanent
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Salary: On Application
BACKGROUND Our client has a well-earned reputation for introducing innovative and effective medicines for disease areas in need of new therapies - particularly in oncology, transplantation and ophthalmology. They are also known for producing new and ever-more efficient medicines for the more common cardiovascular and respiratory diseases, as well as for diseases affecting the brain. They have one
Requirements: and acting as chief investigator on Phase II-IV trials for pipeline developments. Based at the company’s offices in Surrey.
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Outsourcing Manager for Investigator Grants and Academic Partnerships. The purpose of the job is to: Set up... strategies for investigator grant spending and academic partnerships and other clinical categories as needed... or as significant events dictate, and is endorsed by Senior functional stakeholders. 3. Set up and conduct projects... the projects according to the expectations of the Functional Stakeholders, Analyzing key investigator groups
Contract: Permanent
), investigator-initiated research projects and named patient programmes. o Input into reviews and sign off... advisor, medical adviser, senior medical advisor , senior medical adviser , medical affairs , head
Requirements: Top 3 Pharmaceutical Company. International role with a particular focus on Asia Pacific, Japan and Emerging markets. We are looking for a Senior Medical Lead to support their important and high profile portfolio of products in the area of Diabetes
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Job Summary: Excellent opportunity for a Senior Statistician to join a Global Biologics company... . Requirements: Senior Statistician, Cambridge, Permanent Role Our client is a global biologics company... with the flexibility to work from home. Main duties / responsibilities of the Senior Statistician To provide expertise... considerations at investigator or other external meetings. Participate in the preparation, review and approval
Contract: Permanent
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specifications; provide study-specific training and leadership to clinical research staff, CRO, CRAs, sites and other contract personnel. You will plan, execute and lead study-specific meetings (e.g. investigator meetings, advisory... options call Joanna Nelley on 0208 --- ---0 Keywords: Clinical Project Management / CPM / Clinical Management / Senior CPM / Contract CPM / Study Management / Global Study Manager / Clinical Research Jobs - AXCRJ / Interim Roles
Requirements: An opportunity to lead a team on a global Phase III study in the Neurosciences. A unique project management role available for an individual with experience in global Phase III study. You will be capable of driving new initiatives and influencing internat
Jobs similar to "senior investigator": senior investigator recruitment manager, senior financial investigator manager, senior financial investigator, financial investigator manager
Our client, an exciting and rapidly expanding pharmaceutical company are currently seeking a Senior... RESPONSIBILITIES include: ⢠Working with the CRO in setting and negotiating investigator fees ⢠Working... in the management and setting up of investigator meetings ⢠Providing internal support with regards to study... invoices with respect to investigator payments and collate them to the eCRF ⢠Work with the CRO
Experience: N/A
Contract: Temporary/Locum
Salary: On Application
and require experienced, high calibre Senior Clinical Study Managers / Clinical Project Managers A fantastic... and clinical study report preparation Organize and conduct Investigator Meetings Review of ongoing summary data... and medically consistent data Investigator selection and site management Prepare and negotiate study budgets
Requirements: We are recruiting on behalf of a Pharmaceutical organisation with a developing pipeline in Oncology for their International Office based in Switzerland. A fantastic working environment with an open, supportive team culture. Excellent transport links to th
and talents of our people and they are truly what set us apart. Job Title: Study Authorisation Associate Senior Department: ICON Submissions and Investigator Services (ISIS) Location: EU Role Responsibility Working within a highly
Experience: 4 years
Contract: Permanent
and sometimes interpreting results to present to senior colleagues. These experiments will include: " Testing the performance of the mechanical, electronic and optical sub-systems that make up the prototypes " Testing the performance... you will be required to have a CRB check. You will be required to follow strict safety procedures. This role will report to the Project Leader/Clinical Investigator. Key skills/experience: 1. Be practical with good hands