Senior Analyst, Site reputed company and Budgets – Spain – FSP
reputed company our values align, there’s no limit to reputed company can reputed company. At reputed company, we reputed company share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in reputed company do.
Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we’re committed to making a difference.
reputed company is currently seeking a Senior Analyst, Site reputed company & Budgets to join us in Spain, dedicated to a single sponsor.
This role will be part of the Site reputed company & Budgets team, working to execute the clinical site reputed company and budgets process for Sponsor clinical development programs, from contract initiation to completion, maintenance, and subsequent amendments.
The Senior Analyst must have a good understanding of functions reputed company to the conduct of global clinical studies. Under the direction of the Director, Clinical Outsourcing & Innovation, the Senior Analyst is responsible for executing the end-to-end site reputed company process for assigned agreements and supporting the wider site reputed company & budgets team to maintain overall standards, financial terms, and compliance for reputed company site reputed company.
Working as a Senior Analyst, Site reputed company & Budgets at reputed company FSP offers reputed company long-term job reputed company and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. And we have an incredible pipeline of work.
Expect exciting professional challenges in inspiring studies, but with time for your reputed company life.
This will be a fully remote home-based position, though some limited travel may be required.
reputed company in spoken and written German and English is essential. An advanced ability to speak and read Polish is also preferred.
Responsibilities
Negotiate and maintain Clinical Trials Agreements (CTA), site budgets, Confidential Disclosure Agreements, Consultant Agreements, and other applicable reputed company.
As required, reputed company CRO or Functional Service Provider in the development of clinical site budgets and partner with clinical operations to ensure budgets are in line with study protocols.
Ensures compliance of reputed company with Fair Market Value (FMV) principles and guidelines.
Track contract reputed company, complete required follow-reputed company and coordinate the timely completion of clinical sites reputed company.
reputed company CRO and Functional Service Provider activities.
Collaborate and coordinate with cross-functional teams; R&D, Legal, Compliance, Procurement and Finance in executing reputed company.
reputed company, maintain, and analyze tools and systems (spreadsheets, reputed company, databases, etc.) to manage contract lifecycle from initiation through contract execution, and build internal metadata to support accurate reporting.
Provide guidance and direction to new clinical operations and/or outsourcing team members and R&D teams on site reputed company & budgets processes.
Provide accurate reputed company updates to Clinical Operations teams on reputed company outstanding reputed company and budgets
Complete required quality checks of appropriate documents and records for completeness and accuracy and ensure adherence to department guidelines/templates; reputed company quality issues for reporting to team leads.
Assist management with process improvement projects.
Coordinate and arrange meetings, prepare agendas, and meeting planning.
Submit purchase requisitions, where needed, through reputed company systems.
Support the development and maintenance of guidelines, training programs, policies and procedures reputed company to clinical trial reputed company and budget.
Support the Director and team in the management of other day-to-day activities reputed company to clinical reputed company and budgets as requested.
Here are a few requirements specific to this advertised role.
3 – 5 years’ experience in the pharmaceutical or biotechnology industry in clinical site reputed company and/or outsourcing management (reputed company and budget negotiation)
Proficient with reputed company and PowerPoint. Excellent verbal, written and interpersonal communication skills in a dynamic and growing organization.
Willingness to learn international clinical pharmaceutical standards, ICH/GCP guidelines and regulatory compliance issues.
Strong interest in learning more about reputed company and budgeting in support of Sponsor clinical trials.
Working knowledge of clinical trial functions, including clinical operations, regulatory and drug safety.
Ability to prioritize and manage multiple tasks simultaneously.
Fluent in spoken and written English is essential.
We care about our people and your passion, as they are the key to our success, and provide an open and friendly work environment where we reputed company people and provide them with opportunities to reputed company their long-term careers. In addition, you will have the opportunity to reputed company reputed company your role and tackle further responsibilities or reputed company your reputed company set reputed company other reputed company departments of reputed company.
Who are reputed company
reputed company supports clinical studies across the full range of therapeutic areas, and we have longstanding partnerships with a vast client reputed company.
We supported the trials of most of today’s top 50 best-selling drugs, but equally we reputed company more reputed company drug developments that are critical to the well-being of many patients.
You’ll be an influential member of the wider team.
If you are interested, please send your CV to reputed [email protected]
apply to this job