Study Start-Up Project Manager (Finance)

Fortrea; Maidenhead; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading clinical research organization in Maidenhead is seeking an experienced professional to oversee local operational clinical trial activities. The role involves managing trial commitments, ensuring regulatory compliance, and collaborating with various stakeholders. Candidates should have a university degree and at least 4 years of relevant clinical research experience. Competitive compensation and career growth opportunities are offered.

Qualifications

• Minimum 4 years of clinical research experience in pharmaceutical or CRO.
• Thorough knowledge of ICH Guidelines and GCP.
• Fluent in English and local language, both written and verbal.

Responsibilities

• Manage country deliverables, timelines, and results for assigned protocols.
• Oversee clinical trial country submissions and approvals.
• Collaborate with internal and external stakeholders.

Skills

Good organizational and time management skills

Excellent communication skills

Detail and process oriented

Self-motivation

Positive attitude

Flexible and adaptable

Education

University degree in life sciences or related field

Certification in allied health profession

Tools

Computer skills

Job description

Job Overview:

Accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight, and impact on local regulatory and financial compliance, at a country operations level at the client. The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up. The ability to indirectly influence investigators, vendors, external partners, and country managers to deliver these commitments is a must. This includes adhering to budget targets and agreed payment timelines, addressing and resolving issues, maintaining expertise in country-based regulations, laws and procedures with minimal support from the client management. Requires skilled knowledge of budget and contract negotiations, the local ethics, legislation and regulatory environment, submission and approval processes, development of local Informed Consent as well as other site ready and ongoing study deliverables. Ability to proactively develop risk management and mitigation plans in the country and resolve issues locally.


Summary of Responsibilities:

• FINANCIAL (as applicable):
• Assistance with the ownership of country and site budgets.
• Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.
• Oversight and tracking of clinical research-related payments.
• Payment reconciliation at study close-out.
• COUNTRY SUBMISSIONS and LOCAL LANGUAGE MATERIALS (as applicable):
• Responsible for execution and oversight of clinical trial country submissions and approvals for assigned protocols.
• Development of local language materials including local language Informed Consents and translations.
• Works in partnership with IRB/IEC and Regulatory Authority in submission and approval related interactions for assigned protocols.
• MANAGEMENT and QUALITY OVERSIGHT:
• Responsible for managing country deliverables, timelines, and results for assigned protocols to meet country commitments.
• Contributes to the development of local SOPs.
• COLLABORATION:
• Works in close collaboration internally with Clinical country operations (CRD, CRM, CTC, CRA), Country Quality Manager (CQM), Finance, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Business Compliance, Legal and regional operations, Head Quarter functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
• Collaborates closely with Regional Operations to align country timelines for assigned protocols. Provides support and oversight to local vendors as applicable.
• LOCAL PROCESS OVERSIGHT: (as applicable):
• Responsible for clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management.
• Enters and updates country information in clinical, regulatory, safety and finance systems.
• And all other duties as needed or assigned.

Qualifications (Minimum Required):

• University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
• Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
• In lieu of the above requirement, candidates with a minimum of four (4) or more years of relevant clinical research experience in pharmaceutical or CRO industries or experience in a health care setting will be considered.
• Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries
• Thorough understanding of the drug development process
• Fluent in local office language and in English, both written and verbal

Experience (Minimum Required):

• Good organizational and time management skills.
• Working knowledge of ICH, FDA, local regulatory requirements, IRB/IEC and other applicable regulations/guidelines; familiarity with investigator start up documents; previous interaction with operational project team and investigative sites preferred.
• Excellent communication skills, oral and written.
• Self-motivation with the ability to work under pressure to meet deadlines. Works well independently and in a team environment.
• Detail and process oriented.
• Positive attitude and approach.
• Interact with internal and external customers with a high degree of professionalism and discretion.
• Multi-tasking capability.
• Good computer skills with good working knowledge of a range of computer packages.
• Ability to lead and develop junior staff.
• Flexible and adaptable to a developing work environment.
• Minimum of four-six (4-6) years of clinical research experience.

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