Site Start Up Specialist at Parexel

Guangzhou City, Guangdong Province, China -

Full Time

Start Date

Immediate

Expiry Date

12 Jul, 26

Salary

0.0

Posted On

13 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical trial management, Site activation, Regulatory document management, Informed consent form negotiation, Problem-solving, Project planning, Communication, Time management, CTMS, eTMF, ICH-GCP compliance, Stakeholder management, Data quality assurance, Analytical skills, Mentoring, Attention to detail

Industry

Pharmaceutical Manufacturing

Description

When our values align, there's no limit to what we can achieve. At Parexel, we all 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 what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Key Accountabilities: Start-up (from site identification through site activation): Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase. Build relationships with investigators and site staff. Support on request country specific feasibility and/or site pre-qualification and qualification activities, which may include: Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA) and any amendments. May conduct remote Qualification Visits (QVs). Liaison with stakeholders to understand Clinical Site Agreements (CSA) timelines. Manage country and site level TMF issues ensuring documents’ First Time Quality (FTQ) as well as providing direct resolution to reported site problems. Develop strategy to configure, distribute, collect, and review and approve, high quality country specific and/or site specific documents or essential regulatory documents (Site SIV Readiness/Greenlight Documents) and any updated or amended regulatory documentation. Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval. Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy. Forecast, develop, manage, and revise plans and strategies for: IRB/IEC and MoH / RA submission/approval, Site activation, Update and maintain appropriate Clinical Trial Management System (CTMS) in a timely manner. Promptly identify, use judgment and knowledge to address and resolve or escalate, any site question and/or issue, including but not limited to: potential issues or risks with site activation timelines, issues with patient recruitment strategy, deficiencies in training, data quality or integrity, study non-compliance, etc. Facilitate and support allocated sites with access to relevant study systems and ensure they are compliant with all project specific training requirements prior to study start. Actively participate in internal and/or external meetings as per project needs, Sponsor’s expectations and at Manager discretion Work in a self-driven capacity, with limited need for oversight. Proactively keep manager informed about work progress and any risk or issues Maintenance (from initiation through close out): Customize, review, and negotiate as needed, country/site specific Informed Consent Forms (ICF), translations (within parameters of country/regulatory/client requirements), and customize and negotiate any amendments as needed during maintenance Prepare and submit IRB/IEC and MoH/RA (if applicable) application(s), resolving conflicts, determining appropriate follow up until receipt of final approval. Forecast, develop, manage, and revise plans and strategies for: IRB/IEC and MoH / RA submission/approval, Submit all pertinent documentation to the trial master file as per project plans/sponsor/company policy. Overall Accountabilities from Site Identification to Close out: Ensure timely and accurate completion of project goals and update of applicable trial management systems with start -up and amendments Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encourage the support of team members where required. Update all appropriate Clinical Trial Management Systems (CTMS) on an ongoing basis including performing regular reviews of country and site level data in clinical systems (e.g. CTMS, and SIS) and ensure timely and high quality data entry compliance from sites, manage and submit all relevant documents to the Trial Master File (TMF), ensuring first time quality, and distribute study documents to site including configuration of Investigator Site Files if applicable and on-going maintenance for completeness and quality. Ensure that assigned sites are audit and inspection ready Monitor and maintain compliance with ICH-GCP and applicable international and local regulations. Show commitment and perform consistent high quality work. Maintain a positive, results-orientated work environment, building partnerships and collaborative relationships, communicating with team(s) in an open, balanced, objective manner, modeling the high performance culture values. Maintain a working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, Parexel SOPs, other Parexel / Sponsor training requirements and study specific procedures, plans and training. Ensure basic understanding of project scope, milestones, budgets, and strive for high quality, timely, and efficient delivery. Provide input and feedback for Performance Development Conversation(s). Proactively keep manager informed about work progress and any risks or issues. Develop expertise to become a subject matter expert. Work in a self-driven capacity, with limited need for oversight. Complete additional tasks in a timely manner (e.g. timesheets, expenses, metrics, etc.) Skills: Demonstrate strong problem-solving skills Able to take initiative and work independently, and to proactively seek guidance when necessary. Excellent presentation skills. Client focused approach to work. Ability to interact professionally within a client organization. Flexible attitude with respect to work assignments and new learning. Ability to prioritize multiple tasks and achieve project timelines; utilizing strong analytical skills to make decision autonomously due to the unpredictable nature of the issues that arise. Strong ability to make appropriate decisions in ambiguous situations. Willingness to work in a matrix environment and to value the importance of teamwork. Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Trial Master File (eTMF) , and MS-Office products such as Excel and Word. Excellent interpersonal, verbal, and written communication skills. Sense of urgency in completing assigned tasks and ability to assist others to meet study/country deliverables. Excellent time management in order to meet study needs, team objectives, and department goals. Proven ability to work across cultures. Shows commitment to and performs consistently high-quality work. Ability to successfully work in a (‘virtual’) team environment. Act as a mentor and role model for other team members. Effectively enlist the support of team members in meeting goals. Attention to detail. Knowledge and Experience: Substantial start up experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology Education: Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

Responsibilities

The Site Start Up Specialist manages the clinical site start-up process, including site identification, regulatory document preparation, and site activation. They act as the primary point of contact for sites, ensuring compliance with ICH-GCP and project timelines throughout the study lifecycle.