Student Veterans of America Jobs

Welcome to SVA’s jobs portal, your one-stop shop for finding the most up to date source of employment opportunities. We have partnered with the National Labor Exchange to provide you this information. You may be looking for part-time employment to supplement your income while you are in school. You might be looking for an internship to add experience to your resume. And you may be completing your training ready to start a new career. This site has all of those types of jobs.

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  • Jobs on this site are original and unduplicated and come from three sources: the Federal government, state workforce agency job banks, and corporate career websites. All jobs are vetted to ensure there are no scams, training schemes, or phishing.
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  • The newest jobs are listed first, so use the search features to match your interests. You can look for jobs in a specific geographical location, by title or keyword, or you can use the military crosswalk. You may want to do something different from your military career, but you undoubtedly have skills from that occupation that match to a civilian job.
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hVIVO - Whitechapel Clinical Biosample Operation Expert in Netherlands

Venn Life Sciences, part of Open Orphan plc, is an integrated drug development partner offering a unique combination of pre-clinical and CMC drug development expertise with clinical trial design and trial management. This enables us to create, plan and execute drug and medical device development programs effectively and seamlessly for our clients.

Our vision is to play a pivotal role in the development of new products enabling disease prevention and treatment. We do this by creating an environment that generates opportunities for employees to stretch their potential and fully exercise their talents thereby consistently providing outstanding services to our clients. We nurture an environment of respect, pro activity, teamwork and above all keep the patient at the heart of what we do.

We are looking for a Clinical Biosample Operation Expert to join our team and be a member of our clients’ international study teams.

You will be responsible for the global coordination and logistics of human clinical samples (biosamples) in a fast-paced and complex international setting with internal and external interfaces in compliance with regulatory requirements and Good Clinical Practice (GCP). Your tasks will include designing, planning, executing, coordinating, and monitoring all logistic aspects and activities (collecting and handling samples, shipments, storage, and data reconciliation) regarding all biosamples for various areas (pharmacokinetics, biomarkers and biobanking) independently. This role concerns a responsibility for biosample management activities outsourced to third parties.

Responsibilities & Accountabilities:

  • Record and compile the highly complex analytical and technical biosample and study requirements in plans and checklists based on the clinical trial protocol. Coordinate, harmonise and optimise this information with internal and external interfaces regarding content, scope, time, costs and regulatory requirements

  • Perform reviews and add required specifications in relevant study-specific documents such as the clinical trial protocol and the electronic case report form and update them regularly

  • Obtain and review offers for commissioning a logistics supplier in close cooperation with stake holders (e.g., project leaders). In particular: specify the work packages to be commissioned, ensuring that the sample logistics aspects are correct and complete and approving the content of the contractual documents

  • Independent, timely and target-oriented communication with the logistics supplier.

  • Coordinate, monitor and steer sample logistics including cost plans and schedules, considering all functions and interfaces involved

  • Specify and perform the data reconciliation between the logistics supplier and sponsor, develop solutions in the event of discrepancies, coordinate measures with the relevant interfaces

  • Determine causes, assess effects, initiate measures, document and communicate to all relevant functions in the event of deviations

Qualifications & Experience:

  • BSc or higher-level qualification in life sciences or other relevant discipline

  • At least 2 years’ experience in clinical trials

  • At least 1 year project management experience in a project management or combined project management/CRA role

  • Project management experience in logistic arrangements / requirements of human clinical trial samples, e.g., pharmacokinetic samples, biomarkers and biobanking

  • Experience in working with vendors in a global setting

  • Knowledge of GCP and other relevant regulations

  • Understanding of the clinical trial environment including regulatory requirements are of benefit.

Skills:

  • Ability to work independently and as part of a team

  • Excellent attention to detail, planning & organisational skills

  • Ability to find effective solutions or seek internal advice to deal with more complex matters

  • Results and quality-oriented with the ability to multi-task, establish priorities, manage workload and meet strict deadlines

  • Ability to anticipate potential issues and problems that may arise and proactively identify ways to resolve/mitigate

  • Good influencing and collaboration skills, particularly across a multicultural organisation

  • Team member with ability to communicate effectively and form positive relationships in and outside the company

  • Demonstrates good judgement and decision-making capability

  • Flexibility to travel and work at different locations

  • Excellent written and verbal communication skills including excellent command of English.

If this seem like you then follow the link to our website and connect to show you interest,

iCIMS ID: 2022-2639

Address Line 1: Lage Mosten 29

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