Clinical Research Lead - single-client - Germany

Syneos Health; Deutschland; Vor Ort; EUR 110.000 - 140.000; Vollzeit

Zusammenfassung

Syneos Health is seeking a Clinical Research Lead for a single-client engagement in Germany. The role requires deep collaboration with local, regional and global stakeholders, overseeing site management, monitoring and data integrity with focus on patient safety and regulatory compliance.

You will coordinate cross-functional teams, drive risk mitigations, and lead the development of study tools and templates, including monitoring plans, to ensure timelines and budgets are met.

Qualifikationen

• Extensive collaboration with internal and external stakeholders across Germany.
• Oversee site management oversight, clinical monitoring and central monitoring.
• Ensure patient safety, protocol/GCP/regulatory compliance and data integrity.
• Identify risks to trial management deliverables and propose mitigations.
• Develop and maintain clinical study tools and templates, including the Clinical Monitoring Plan.

Aufgaben

• Join single-client partnership as CRL in Germany.
• Act as networking hub with local, regional, and global colleagues and external partners.
• Oversee site interactions from activation to closeout.
• Escalate risks to project manager for timeline, quality, budget.
• Coordinate training, dashboards, and data plans for the study.
• Ensure CTMS and audit trails are set up and tested.
• Coordinate resourcing for CRAs and Central Monitors.
• Collaborate with Study Start Up, Patient Recruitment and Data Management.
• Attend Kick Off Meetings and other key stakeholder meetings.

Kenntnisse

Clinical research leadership

Stakeholder collaboration

Site management oversight

Risk management

Data integrity

Tools

CTMS

Dashboards

Jobbeschreibung

Clinical Research Lead - single-client - Germany

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone's life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

• For one of our single-client partnerships we are currently looking for a Clinical Research Lead to join the team here in Germany.
• The Clinical Research Lead (CRL) role is highly integrated into our clients' organization and requires extensive collaboration with a broad range of internal and external stakeholders. The individual serves as a key networking and coordination hub, working closely with local, regional, and global colleagues as well as external partners across Germany.
• Responsible for site management oversight, clinical monitoring and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance and data integrity.
• Oversees site interactions post activation through site closeout. This may include patient recruitment, investigator payments or other related activities.
• May be responsible for identification of critical data and process, protocol execution risks and risk mitigations related to completion of the Risk Assessment and Categorization Tool (RACT).
• Reviews the study scope of work, budget and protocol content and ensures the clinical project team (CRAs/Central Monitors) is aware of the contractual obligations and parameters.
• Uses prior clinical experience, operational data, metrics and reports to identify risks to clinical trial management deliverables.
• Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget) and any activities and requests which are out of contracted scope.
• Employs strategic thinking and problem-solving skills to propose and implement risk mitigations.
• Participates and presents in key meetings such as Kick Off Meeting.
• Serves as an escalation point for communications with investigator site staff and may be required to interact on the phone or in person with principal investigators or other site staff members. This may include accompanying CRA team members to sites for observation or conflict resolution.
• Collaborates with other functional leaders such as Study Start Up, Patient Recruitment and Data Management to coordinate delivery handoffs and meet expected study milestones such as site activation targets, enrollment targets and database lock timelines. Reviews and provides feedback on other functional plans (e.g. Data Management Plan, Communication Plan) as they relate to the clinical trial management activities.
• Responsible for development and ongoing maintenance of clinical study tools and templates, including the Clinical Monitoring Plan. Ensures CTMS, dashboards and other systems are set up and available for use by the clinical team, including overseeing user acceptance testing (UAT) as needed. Ensures access and audit trail reviews are conducted as required.
• Coordinates initial and ongoing training to the study team regarding protocol specificities, Case Report Form (CRF) completion, dashboards, Sponsor Standard Operating Procedures (SOPs), clinical plans and guidelines, data plans and timelines for the study.
• Oversees resourcing allocations for CRAs and Central Monitors, site assignments and study team members' conduct, and identifies risks to delivery or quality.
• Ensures quality of the clinical