Lifelancer is an AI-powered platform for talent hiring in Life Sciences, Pharma, Healthtech & IT.
The platform connects employers with freelance, remote & international talent and focuses on pharma, biotech, health sciences, healthtech, digital health & IT domains.
You can quickly connect with top talent and 25,000+ experts in the above domains at Lifelancer.
Lifelancer also facilitates international hiring compliance & payroll services in collaboration with market-leading partners.
The platform aims to empower life science & IT talent as well as life science startups & SMEs.

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Lifelancer is an AI-powered talent hiring platform that connects employers with skilled professionals in the Life Sciences, Pharmaceutical, and IT sectors. It enables individuals to create profiles showcasing their skills, get matched with high-paying international jobs or projects, and facilitates hiring and payroll for employers in multiple countries. The platform aims to streamline the hiring process with efficient AI sourcing and compliance support.

Lifelancer is an AI-powered platform for talent hiring in Life Sciences, Pharma, Healthtech & IT. The platform connects employers with freelance, remote & international talent and focuses on pharma, biotech, health sciences, healthtech, digital health & IT domains. You can quickly connect with top talent and 25,000+ experts in the above domains at Lifelancer.

Lifelancer also facilitates international hiring compliance & payroll services in collaboration with market-leading partners. The platform aims to empower life science & IT talent as well as life science startups & SMEs.

• Manage, administer, and organize local site operations for a Clinical Pharmacology unit, potentially across multiple sites
• Ensure overall site performance, defined metric goals, and Sponsor needs are met
• Serve as a lead member of the site leadership team and provide an active voice for all sites
• Ensure efficient utilization of human and physical resources
• Partner on improvement initiatives with Clinic Directors and Operations Directors
• Present Fortrea capabilities to clients and lead growth within assigned clients
• Own assigned client relationships, expectations, and satisfaction
• Lead RFI/RFP responses, proposal development, bid defense preparation, and presentations
• Establish new partner relationships and leverage growth opportunities
• Support Fortrea capability, visibility, and position through publications, conferences, meetings, and webinars
• Proactively plan client work pipelines and partner with business development to achieve sales margins
• Define, drive, and implement strategic initiatives with Therapeutic Area leadership
• Ensure consistency of quality, standards, policies, processes, and practices across client projects
• Represent partnerships and serve as a client advocate within Fortrea
• Build a sustainable and scalable Alliance management client model
• Lead in a global, complex environment; set expectations; coach and mentor for success
• Lead and present at Operational Governance meetings
• Facilitate Executive Committee meetings and follow up on action items
• Conduct timely NPS surveys and maintain client satisfaction
• Lead Lessons Learned initiatives
• Lead, manage, facilitate, and expedite activities across Fortrea divisions supporting partnership success
• Ensure delivery meets client quality, timeline, and budget expectations
• Ensure projects are appropriately resourced according to contractual obligations and client fit
• Maintain cost performance index at or above 1.0
• Develop and deliver client-specific training
• Ensure client-specific process improvement efforts maximize portfolio efficiency
• Perform other duties as needed or assigned

Senior Clinic Director – Phase I CRU

Senior Clinic Director leading Fortrea’s multi-site clinical pharmacology operations and client partnerships. Driving clinical research delivery, governance, growth, and client satisfaction across US and Canada.

clinical-research

• Lead clinical data management studies involving healthy volunteer and patient populations, multi-site studies, complex protocols, client management, or reduced timelines
• Own data management deliverables from study start-up through database lock
• Develop project documentation, system setup, data entry, and data validation procedures
• Build timelines with Project Managers or FSP Leads to meet contracted milestones
• Lead data-focused internal project team meetings and coordinate deliverables across EDC Design, SAS Programming, Statistics, and PK
• Identify risks and mitigations and communicate data-driven discussions to achieve database lock dates
• Coordinate receipt and inventory of data from clinical sites and vendors
• Ensure projects follow protocols, global harmonized SOPs, GCP standards, DMPs, and scope of work
• Maintain client relationships, review satisfaction surveys, and implement action plans and process improvements
• Track scope changes and secure Sponsor approval
• Provide leadership, mentorship, coaching, training, and performance feedback to data management staff
• Reconcile clinical databases against safety, laboratory, and third-party data
• Utilize local laboratory systems and batch data load facilities
• Support new business opportunities, bid defense meetings, audits, and sponsor-facing Biometrics activities
• Contribute to SOP development and maintain accurate work records
• Keep stakeholders informed about project progress, budgets, scope changes, and timeline impacts

Senior Clinical Data Manager – Oncology

Senior Clinical Data Manager leading oncology clinical trials at Fortrea, a global clinical research organization. Owning data management from study start-up through database lock.

operations

• Manage the receipt and processing of adverse event reports from spontaneous sources and clinical trials
• Enter safety data into the safety database and review adverse events
• Write patient narratives with coding
• Follow up on missing information
• Assess cases against the appropriate product label for marketed products, if applicable
• Submit expedited Serious Adverse Event reports to clients, regulatory authorities, ethics committees, investigators, third-party vendors, partners, and Fortrea project personnel when required
• Prioritize cases requiring expedited reporting and ensure submission within regulatory and study-specific timelines
• Work with Data Management or clients on reconciliation of safety databases, when appropriate
• Support audit or inspection preparations
• Coordinate workflow activities across safety operations
• Monitor case progression and compliance metrics
• Identify and resolve workflow delays
• Ensure efficient utilization of resources and high-quality service delivery
• Provide operational support to client project teams and standalone programs
• Comply with applicable pharmacovigilance regulations, company procedures, quality standards, and health and safety requirements
• Perform other duties as assigned by management

Workflow Manager, Pharmacovigilance Operations – Specialist II

Pharmacovigilance workflow manager overseeing adverse-event workflows, expedited reporting, and safety database reconciliation. Supporting Fortrea clinical-trial and post-marketing drug-safety operations.

Lifelancer is an AI-powered platform for talent hiring in Life Sciences, Pharma, Healthtech & IT. The platform connects employers with freelance, remote & international talent and focuses on pharma, biotech, health sciences, healthtech, digital health & IT domains. You can quickly connect with top talent and 25,000+ experts in the above domains at Lifelancer. Lifelancer also facilitates international hiring compliance & payroll services in collaboration with market-leading partners. The platform aims to empower life science & IT talent as well as life science startups & SMEs.

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3 jobs found

Senior Clinic Director – Phase I CRU

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Senior Clinical Data Manager – Oncology

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Workflow Manager, Pharmacovigilance Operations – Specialist II

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