Global clinical project manager - homebased, any eu country - global - united kingdom, united kingdom

global clinical project manager - homebased, any eu country - global pharmaceutical

upsilon global are currently seeking a global clinical project manager with experience leading both local and international studies across europe and america. our partner is a well-established, global pharmaceutical with an exciting portfolio of studies within oncology, vaccines and immunology. they re seeking experienced and highly motivated global cpms to join their teams and help deliver world-class clinical research as quickly and effectively as possible.

background

details confidential, information available upon request. if you ve got experience delivering fast-paced international projects, are looking for greater autonomy and responsibility, and have the drive to work independently, this is a great opportunity for you. you ll be working as part of a small but close-knit european team to deliver some best-in-class programmes. collaborating with a us-based executive team, you will have sole responsibility for the delivery of key clinical projects.

main responsibilities

the successful and timely delivery of pan-european (and us) clinical studies

regularly planning tasks to meet clinical program: timelines, budgets and high quality standard

tracking program budget as well as reviewing and approving invoices

being the first point of contact for program related issues (both internally and externally)

implementing, monitoring and supervising assigned clinical program

ensuring all tasks are in line with the gcp standards supervising and maintaining tmf strictly complying with the internal sops leading and coordinating the clinical project team

interacting with cros and trial sites to ensure sponsor's oversight responsibilities

developing sections of clinical trial protocols and related documents with internal stakeholders and cros supporting the head of clinical operations and director of business development with activities when necessary

sharing information about clinical trial updates for both internal and external team meetings using

microsoft office tools (this will include regular updates, investigator's meeting and cra training)

developing clinical section of regulatory documents

travelling internationally as required

education and qualifications

a masters or bachelor s degree within a lifescience associated field cro, pharmaceutical and medical device experience

proven track-record in the successful delivery of international clinical studies, experience working with us based clients is preferable

strong knowledge of clinical research, preferably progressing from a field-based cra into study/project management

other skills and abilities

in depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., good clinical practice (gcp) and international conference on harmonisation (ich) guidelines strong communication and interpersonal skills, including good command of english good presentation skills ability to establish and maintain effective working relationships with co-workers, staff and clients

for further information on this opportunity and to learn of similar positions, please contact alessandro asproso . 20. 3. 8. 75. 99. 6. 6 or email applications (at)

upsilon global welcome all enquiries and will offer a no obligation discussion regarding your present situation. this vacancy is being advertised by upsilon global ltd, a uk registered employment consultancy. upsilon global ltd act in the strictest of confidence on behalf of both candidates and clients.

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