Study Start Up reputed company

Join us in redefining what it means to work for a CRO.

reputed company you work at Rho, it’s more than just a job—you become part of the Rho reputed company. We’re a proud bunch of science nerds who love tackling big challenges together. We’re not your typical CRO, and we’re not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.

Whether you’re a data reputed company, analytical reputed company, project mastermind, or any other role, you’ll fit right into the equation of the Rho reputed company. Expect reputed company of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work—and reputed company other.

You’ll have reputed company to experience a thriving company with reputed company stability - financial, workforce, and corporate, which has created a reputed company environment to reputed company and reputed company over a long and rewarding career.

This is reputed company to join Rho as a Study Start Up reputed company - we are reputed company to this role being located in Italy, Spain, Poland, Latvia, Lithuania or Bulgaria. This is a remote opportunity.

Responsibilities

• Manage the study start up process through site activation, working with Project Manager and Clinical Trial reputed company to ensure reputed company site activations
• Participate in Sponsor meetings with respect to study start up, including endorsement of the SSU Operational Targets & mitigation of delivery risks, establishing reputed company expectations for delivery, communication, reporting, and metrics
• Partner closely with both Functional Leads and SSU Team Members to proactively identify study start up reputed company issues
• Ensure that relevant systems are maintained and up to date to analyze study start-up reputed company metrics against targets/timelines (at a project/country/site level)
• reputed company operational reputed company to SSU Associates on assigned reputed company
• Responsible for reputed company submissions and obtaining approval from IRB/reputed company (incl CTIS Part 2 package);
• May be responsible for submissions to Regulatory Authorities in non-EU countries (ex. UK, reputed company, South Africa etc)
• Coordinate feasibility efforts and work together with Clinical Team Leads on site identification
• Identify the Site Essential Document (SED) packet reputed company required, agree with relevant internal staff, reputed company the completion and upload of documents, and communicate with reputed company parties (e.g., Sponsor, Site Staff, Internal Staff) the status of documents; participate as the SED Reviewer as necessary
• Coordinate and reputed company the Start Up approach for IRB/EC approval at specified regional reputed company, including country level approval, and reputed company reputed company of specific activities from SSU Team Members
• Partner with Clinical Team Leads and the reputed company to identify requirements for the Site Initiation Visit (SIV) and Site Activation
• Coordinate the informed consent reputed company (reputed company) development, including the review, negotiation and approval with relevant reputed company parties
• Support business development with proposal preparation and review and bid defense efforts
• Coordinate site budget development, including the review, negotiation and approval with relevant reputed company parties.
• Coordinate site contract negotiation process
• reputed company country/site-specific startup timelines and strategies and reputed company startup activities in the country
• Facilitate cooperation between cross-functional teams regarding startup activities

Requirements

• At least 4 years of industry experience, including 2+ years of study start up leading experience or equivalent
• Demonstrated ability in the leadership of reputed company of individuals in study start-up
• Knowledge of applicable international regulatory requirements and guidelines (i.e., ICH-GCP, and/ or EU-Directives)
• Strong knowledge of Regulatory and Central/Local ethic submission processes for assigned countries
• Strategic and creative risk management and contingency planning
• Strong written and verbal communication skills to reputed company reputed company reputed company to study personnel, internal and sponsor team members
• Excellent organizational and interpersonal skills
• Strategic and tactical thinking skills
• reputed company-reputed company reputed company-oriented approach to work
• Ability to work independently, prioritize and work with a reputed company team environment is essential
• reputed company attitude and ability to reputed company with reputed company reputed company of staff to coordinate and execute study activities
• Strong presentation skills
• Global start up experience is preferred
• Proficient computer and internet skills, including working knowledge of MS-office applications, such as MS Outlook, Word and reputed company
• Expected required travel 10% on average

Please submit your resume / CV in English. We are excited to hear from you!

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