Clinical Trial Health Authority application and regulatory submission process.
Contracts & Indemnity request process.
For global studies, localize global Informed Consent Form (ICF) with country requirements.
Local sample application and permit submission processes.
Maintain up to date knowledge, ensure adherence and compliance with local regulatory requirements and associated documentation.
Review, analyze and collate metrics to ensure processes are in place that drive efficiency and reduction of timelines across start up and contracts negotiation.
Ensure all start up information & requirements are kept up to date in a central repository for both global and local Study teams.
Assist with label preparation and approval (local label representative) for studies in
collaboration with local regulatory department.
Track metrics and study start-up timelines to identify trends and opportunities for
Liaise and collaborate with relevant authorities / bodies to further enhance clinical trial processes, government policies / laws, via innovative approaches.
Maintain currency and awareness of changes in Start Up processes across government, hospital & industry & liaise with stakeholders to resolve any SSU issues.
Proactively respond to information survey requests by government/industry bodies.
Provide continuous and proactive communication with ECs/hospital administration/industry bodies to obtain accurate and up to date information on clinical trial status and activities.
Maintain communication with local legal/regulatory/clinical operation to ensure input is sought and all internal/external requirements are met.
Provide guidance to CSMs and CSS on regulatory/ethics, track & drive site activations by regular review and monitoring status of submissions/activations.
In collaboration with vendor management and procurement, provide input as required into vendor identification, selection, and RFI/RFP process.
Liaise and share best practices with other SSU within the region/organization.
New Site Identification:
Assist with identification and tracking of new sites in collaboration with CSMs.
Perform/coordinate site level feasibility activities including evaluation of patient
population and final site selection.
Provide expertise and guidance to Global and/or Local Study Team (LST) for identification, creation and implementation of specific recruitment/retention tactics & contingency planning.
Initiate patient recruitment meetings with CSM and advise on study-specific recruitment & retention needs.
Develop innovative patient recruitment/retention practices and share concepts with vendors as needed.
Provide justification/recommendation of site closure in collaboration with CSM.
Provide reports to local study teams on overall site performance as required.
Negotiate contracts and study budgets with sites during the study start-up phase to ensure finalization.
Provide local fee structures and budgetary advice as required and ensure compliance to Fair Market Value (FMV) in the country.
Collaborate with CSMs to maintain data to ensure FMV
Liaise with management / Country Study Managers (CSM) to implement budget cost containment and implement contingencies as required.
University Degree or Equivalent preferably in a medical/science-related field.
Prior work experience demonstrating knowledge and understanding of clinical trials, such as that obtained in a clinical trial monitor capacity, and experience managing projects.
Demonstrated knowledge and understanding of ICH-GCP, the regulatory, ethics and contractual requirements for starting clinical trials in relevant country.
Skills, Experience and Competencies:
Demonstrated competence in analysis, planning and problem solving.
Excellent communications skills including the ability to state opinions clearly, ask questions, seek clarification, communicate facts objectively, challenge when appropriate, and pursue issues to resolution.
Ability to present clear messages from complex information/data to all levels in the organization in both written and spoken English.
Experience working as part of a team with a proven ability to make an active contribution to the team’s performance and teamwork.
Able to make effective decisions, self-motivated, assertive, and displays initiative
Proven project management and organizational skills and the ability to prioritize and manage multiple tasks with flexibility.
Demonstrated computer literacy, usage of MS Office software, web-based systems and databases.
Availability to travel domestically and internationally if required.
Who We Are
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry
for more than 40 years, using human genetic information to develop novel medicines for serious and
life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious
illnesses. Please take this opportunity to learn about Genentech where we believe that our employees
are our most important asset & are dedicated to remaining a great place to work.
The next step is yours. To apply today, click on the "Apply online" button.
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At Genentech, we share salary ranges with applicants during the recruiting process, if requested. Third party salary estimates may not be accurate or up-to-date.