Study Manager, Clinical Operations

Orchard Therapeutics plc.; Greater London; On-site; GBP 70,000 - 110,000; Full time

Job summary

Orchard Therapeutics plc. is a global gene therapy leader headquartered in London, England. The Clinical Operations Clinical Study Manager will oversee operational management for multiple trials, drive planning, budgeting and data integrity while ensuring patient safety and regulatory compliance.

Reporting to the Director of Clinical Operations, this role requires leadership, cross-functional collaboration and occasional international travel to meet study objectives and vendor milestones.

Qualifications

• Proven experience in pharma/biotech clinical operations and trial management.
• Experience with regulatory environments (GCP/ICH) and vendor oversight.
• Strong organizational, communication and leadership abilities.

Responsibilities

• Lead and manage clinical study activities across multiple trials.
• Collaborate with CROs, vendors and cross-functional teams to meet milestones and budgets.
• Ensure upfront planning, protocol input and feasibility assessments.
• Oversee budgeting, forecasting and financial reconciliation for studies.
• Maintain study documentation according to regulations and SOPs.
• Mentor junior team members and participate in process improvements.
• Travel approximately 20% for study meetings and site visits.

Skills

Organizational skills

Communication skills

Leadership

Collaboration

Business English

Education

BSc Life Sciences

MSc/PhD preferred

Job description

Location : London

Reporting to : Director, Clinical Operations

Orchard Therapeutics, a Kyowa Kirin company, is a global gene therapy leader focused on transforming the lives of patients with rare disorders through innovative gene therapies based on gene-modified hematopoietic stem cells (HSCs). Orchard has its global headquarters in London, England, and its U.S. headquarters in Boston, Massachusetts.

Job Summary

The Clinical Operations Clinical Study Manager will be accountable for managing the clinical operation activities for approximately 2 to 3 clinical trials depending on the complexity of the trial and lifecycle of the trial as it pertains to resource needs. This person will be key in driving strategic clinical trial operational planning, clinical studies day to day activities including budget management, ensuring on time delivery of main clinical milestones, and most important ensuring patient safety and data integrity while following internal SOPs and ICH/GCP requirements.

Key Responsibilities

• Lead and manage clinical study/studies according to global regulatory requirements (including but not limited to US CFR, EU CTD/CTR, and ICH GCP) and Orchard SOPs.
• Collaborate with cross functional study team(s), including Orchard functions, CRO partners and other vendors to ensure study goals are met, on time and within budget. Includes leading and organizing cross functional clinical team meetings.
• Ensure appropriate Clinical Operations input for studies prior to decision making to ensure proper upfront planning.
• Contribute to protocol development, including Clinical Operations feasibility assessments.
• Manage the evaluation and selection of required vendors, including contract and budget negotiation, task orders, change orders, invoice approval and financial reconciliation process, with oversight of Associate Director/Director.
• Responsible for day-to-day management of vendors working on assigned study/studies, including setting expectations, training, oversight process including attending regular meetings and reviewing metric reports, managing timelines and deliverables, and issue management.
• Provide Clinical Operations input to other important study activities, including but not limited to: site identification and selection, enrollment models, clinical supply planning, organization of investigator and vendor meetings, development of informed consents forms and assent forms, planning and management of Trial Master File, development of study plans, development of IxRS systems, development of EDC / Case Report Forms, review of data during the study, data cleaning and database lock, contributing to the Clinical Study Report.
• Escalate medical issues to appropriate Orchard medical personnel.
• Management of study budget and provision of regular budget updates to Finance. This includes forecasting for study budget for years ahead, monthly accruals and quarterly budget reviews as part of the Latest Estimate (LE) process, to ensure the study is conducted within budget and any discrepancies or changes are communicated to the Associate Director/Director who provides oversight, as well as to finance.
• In collaboration with the Clinical Team (Orchard functions, CRO Partners, and vendors), identify risks to study and suggest risk mitigation plans, with oversight of Associate Director/Director, Clinical Operations to escalated risks and ensure rigorous risk mitigation planning.
• Ensure study documentation is maintained according to applicable regulations, industry standards, and SOPs.
• Provide mentorship/management if applicable of more junior members of clinical operations.
• Participate and lead internal process improvement efforts for the department and organization if requested.
• Ability to travel (approximately 20%) which may include overnight and international travel to study meetings, other Orchard sites and vendor sites.

Education / Key Competencies

• BsC in Life Sciences with proven experience working in Pharma/Biotech as well as experience in rare disease areas, pediatric studies and/or gene therapy. (Msc/PhD in life sciences preferred)
• Excellent organizational and communication skills
• Detail oriented
• 'Can-do' attitude and willingness to be flexible
• Demonstrated leadership skills
• Demonstrated collaborative style of working
• Fluent business English (oral and written)
• Experience and knowledge of clinical study/project management
• Experience in oversight of service providers (e.g. CROs, central and specialty labs, etc.)
• Experience leading a clinical trial with a cross functional team
• Understanding of regulatory environment, GCP/ICH and compliance requirements for clinical research

Orchard is an equal opportunity employer. We recognise and celebrate the diverse culture of our workforce and are committed to creating an inclusive environment for our employees. We fully support the principle of Equality and Diversity in employment and oppose all forms of unlawful or unfair discrimination. We assess all applications on basis of job requirements and individual qualifications.

We work within the requirements of all current legislation and we implement the provisions of regulatory codes of practice in employment.

Notice to All Applicants

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