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Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as an Global Study Director - Make an Impact at the Forefront of Innovation

The Global Study Director (GSD) is a business-critical role within Cell Therapy Clinical Operations (CTCO) whose main accountability is the operational planning and delivery of high priority and complex clinical studies within a program, that are deemed most critical to the business. The GSD is responsible for leading a cross-functional study team (core and extended) and for providing the team with direction and guidance to enable successful study delivery. The GSD may provide input to early study planning activities based on operational expertise. The GSD is accountable to the CPT for the delivery of a study, or studies, according to agreed upon timelines, budget and quality standards by ensuring an effective partnership and teamwork within the study team. The GSD will also interface with other internal stakeholders cross-functionally, and/or external partners, to identify, manage and resolve issues affecting study delivery.

The GSD leads the study team(s) and/or study oversight team(s) in accordance with the Study Team Operating Model for Internal Delivery (SOLID), Project Management Framework and/or clinical outsourcing model, current clinical trial regulations (e.g. ICH GCP), Standard Operating Procedures (SOPs), policies and best practices and in line with our values and behaviours.

The GSD is also responsible for providing expert guidance, direction, mentoring, and support to Global Study Managers on their studies, for study specific activities.

What You'll Do:

• Lead and coordinate a cross-functional study team of experts in accordance with SOLID and its roles, accountabilities and responsibilities framework (RACI) to ensure the clinical study progress as planned driving achievement of milestones according to timelines, budget and quality standards.

• Contribute to vendor/ESP selection activities at the study level, including bid defense, and lead operational oversight at the study level in order to ensure appropriate control over the vendor identification and selection.

• Collaborate with other functions to establish strategies and identify synergies aimed at increasing efficiency of global study teams (core and extended).

• Lead and facilitate communication across functions and provide guidance and support to the core and extended study team members as needed and in accordance with study-specific communication plan.

• For outsourced studies, be the primary sponsor point of contact for the CRO Study Manager to ensure study delivery according to agreed upon timelines, budget and quality standards, while ensuring that the appropriate level of oversight of the CRO is maintained and documented throughout the lifecycle of the study, in accordance with relevant SOPs and guidelines (e.g. description of services and transfer of obligations).

• Provide operational expertise into and hold accountability for the development of essential study level documents (i.e. Clinical Study Protocol (CSP) through to Clinical Study Report (CSR)) in accordance with relevant SOPs.

• Ensure all external service providers (i.e. central laboratories, IXRS, ePRO, etc.) engaged at the study level are performing to contracted goals and timelines/budget and that adequate oversight is documented through planning & control activities.

• Develop and maintain relevant study plans (e.g. global study management plan and its relevant components such as study project plan SPP) including required input into study level quality and risk management planning (e.g. risk-based quality management, proactive risk and contingency plans, etc.), ensuring that the risk response strategies and issue escalation pathways are clear to the entire study team.

• Oversee study level performance against agreed upon plans, milestones and key performance indicators (KPIs, quality and operational) by using company tracking systems and project timelines (e.g. SPP, data flow metrics dashboard, CTMS or eTMF dashboard) and communicate any risks to timelines and/or quality to CPT, along with proposed mitigations.

• Providing expert guidance, direction, mentoring, and support to Global Study Managers on their studies, for study specific activities.

• Identify and report quality issues that have occurred within the study in accordance with relevant SOP and collaborate with all functions as necessary to overcome barriers and achieve milestones; proactively communicate findings and corrective action plans (CAPAs) to relevant stakeholders (e.g. CPT, quality assurance staff, functional line management, etc.).

• Oversee Trial Master File (TMF) completion in accordance with relevant AZ SOPs, including ensuring the TMF plan and Expected Document List (EDL) are in place and that QC activities are performed on an ongoing basis to ensure TMF completeness at all times.

• Ensure timely compliance with company-wide governance controls (e.g. Delegation of Authority, Sunshine Act, financial attestations, Clinical Trial Transparency).

• Responsible for study budget re-forecasting following initial budget estimate provided by the CPTand accountable for study budget management through the study lifecycle and for providing budget progress reports to the CPT including any financial risks and mitigation plans (as part of the ongoing study change control process).

• Ensurestudiesareinspection-readyatalltimes,accordingtoICH-GCPandSOPandrelevant policies/guidelines. GSD is the primary CTCO Clinical Operations point-of- contact in the event of an audit or inspection.

• Provideregularfeedbackonindividualperformancetothestudyteammembersandtheirline managers to support their professional development.

• Provideguidance,training,expertinput,mentoringandsupportto lessexperiencedGSL colleagues on an ongoing basis.

• Leads non-drug project work such as CTCO representative in process improvements and/or leading improvement projects as discussed and agreed upon with their manager

Education & Experience Requirements:

· University degree (or equivalent), preferably in medical or biological sciences or discipline associated with clinical research

· Proven project management experience and training

· At least 10 years of clinical trial experience

· At least 5 years of experience in global study leadership and team leadership

·Demonstrated clinical trial expertise in Oncology

Years of experience refers to typical years of related experience needed to gain the required knowledge, skills, and abilities necessary to perform the essential functions of the job. Years of experience are not to be used as the only determining factor in establishing the job class or making employment selection decisions.

Knowledge, Skills, Abilities:

• Comprehensive therapeutic area knowledge, clinical development guidelines and directives and regulatory guidelines

• Expert knowledge of the key principles of cross functional project management (Time, Quality, Cost)

• Excellent oral and written communication and presentation skills

• Demonstrated leadership and interpersonal skills including the ability to lead, motivate and coordinate cross-functional project teams

• Technical and systems competency, such as computer skills, to include effective use of systems and applications such as Microsoft Outlook, Word, Excel and PowerPoint, as well as organization systems (CTMS, Preclarus, Clarity)

• Proven flexibility and ability to effectively prioritize workload and resources for project team members in a frequently changing environment

• Skilled in process improvement and strategic development, especially as it applies to clinical trials, clinical development and project management

• Ability to coach, mentor and lead global and/or cross-functional teams with a cultural awareness

• Strong financial acumen with an in-depth of knowledge and practical application of budgeting, forecasting and resource management.

Project Lead

• Excellent customer service, consultation and relationship building skills

• Advanced negotiation and marketing skills with ability to influence others and drive results

• Excellent judgment, decision making and problem-solving skills and proven ability to apply critical and analytical strategic thinking skills to manage complex/ambiguous situations

• Proactive, solutions oriented and skilled at risk identification and management.

Project Oversight

• Excellent customer service and relationship building skills with the ability to proactively address and prioritize expectations

• Strong executive presence and business acumen

• Advanced negotiation and marketing skills with ability to influence others and drive results

• Proactive, solutions oriented and skilled at risk management

• Excellent judgment, decision making and problem-solving skills and proven ability to apply critical and analytical strategic thinking skills to manage complex/ambiguous situations

• Ability to drive corporate strategies to capture, engage and retain repeat customers People Manager

• Ability to identify and address training gaps for soft skill and technical development, including managing performance stewardship, metrics and retention

• Excellent judgment, decision making and problem-solving skills and proven ability to apply critical and analytical strategic thinking skills to drive development and retention of top performers

• Proven ability to act as a change champion

• Ability to collaborate and foster accountability in a learning environment

• Ability to drive process improvement and strategic initiatives

• Strong negotiation skills with ability to influence others and drive results.

Working Conditions and Environment:

• Work is performed in an office/ laboratory and/or a clinical environment.

• Exposure to biological fluids with potential exposure to infectious organisms.

• Exposure to electrical office equipment.

• Personal protective equipment required such as protective eyewear, garments and gloves.

Why Join Us?

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthroughs.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.