The Contracts & Budgets Associate supports clinical study teams by developing and negotiating study budgets, drafting and negotiating confidentiality agreements, clinical study agreements and amendments, coordinating execution and tracking of contracts, maintaining contract files/databases, and updating stakeholders. Requires a bachelor's degree (or equivalent experience) and a minimum of 1 year relevant contract experience in clinical research or similar industry.

Develops and negotiates European clinical study budgets; reviews, drafts and negotiates confidentiality agreements, clinical study agreements and amendments; coordinates execution and archiving of agreements, updates study teams on negotiation status, and works with stakeholders to resolve contractual issues.

The Contracts & Budgets Associate supports clinical studies by developing and negotiating study budgets, and by drafting, reviewing and negotiating confidentiality agreements, clinical study agreements and amendments. The role coordinates contract execution, maintains contract files/databases, escalates contractual issues to stakeholders, and seeks process improvements. Requires a bachelor's degree (or equivalent experience) and a minimum of 1 year relevant experience in clinical research contract work.

Remote role based in Slovakia. The Contracts & Budgets Associate develops and negotiates European study budgets per study protocols, and reviews, drafts, negotiates and tracks agreements (NDAs, clinical study agreements, amendments). Works with clinical operations teams and stakeholders, maintains contract files/databases, coordinates execution and escalation of contractual issues. Requires a bachelor’s degree or equivalent experience and at least 1 year of relevant contract experience in clinical research.

The role develops and negotiates European/global study budgets based on study protocols, and reviews, drafts, negotiates and coordinates execution of agreements (NDAs, confidentiality agreements, clinical study agreements and amendments). The postholder works with Clinical Operations and other stakeholders to track contracts, maintain contract files/databases, escalate contractual issues, and identify process improvements. Requires a bachelor's degree (or equivalent experience) and at least 1 year of relevant clinical research contract experience.

The Principal Clinical Scientist functions as the CSAI functional lead across study start-up through database lock, providing clinical/scientific input to data capture, review, cleaning, eCRF/EDC activities, UAT, and data visualization. Requires a bachelor's (or equivalent), minimum 8 years clinical research experience, professional English, EDC and eCRF experience; oncology, JReview, database build and global trial experience are preferred. Occasional domestic and international travel is required.

Manage and support Precision’s FSP Site Contracts team, including resource allocation, forecasting, metrics reporting, and adherence to policies. Participate in contract review, drafting and negotiation (confidentiality, clinical study, ancillary, amendments), support FSP business development, act as single point of contact for clients and stakeholders, and line-manage contract and budget associates. Requires at least 6 years' experience in Site Contracts within CROs/FSP and people management experience.

Manage and support the FSP Site Contracts team, act as primary contact for FSP clients and stakeholders, allocate resources and forecast workload, and report on contract metrics. Support drafting, review and negotiation of agreements ( confidentiality agreements, clinical study agreements, amendments ), ensure adherence to policies and contracting standards, and participate in FSP business development initiatives. Requires a 4-year degree or equivalent and at least 6 years' experience in Site Contracts within CROs/FSP models.

Responsible for line managing a team of FSP contract and budget associates, supporting FSP business development, allocating resources and forecasting, reporting contract metrics, and ensuring timely execution and compliance of site contracts. Requires at least 6 years' experience in site contracts within CROs/FSP models and experience in people management.

Manage and support the FSP Site Contracts team, act as primary contact for FSP clients and stakeholders, allocate resources and forecast workload, report on FSP contract metrics, and support drafting/negotiation and execution of confidentiality, clinical study, ancillary and amendment agreements. Requires a 4-year degree (or equivalent) and at least 6 years' experience in Site Contracts within CROs/FSP models, plus people management experience.

Manage and support the FSP Site Contracts team, including people management, resource allocation, forecasting, and reporting of contract metrics. Support and participate in contract review, drafting and negotiations (confidentiality, clinical study, ancillary and amendment agreements), act as single point of contact for FSP clients and stakeholders, and contribute to FSP business development and process improvements. Requires a 4-year degree (or equivalent) and at least 6 years' experience in Site Contracts within CROs/FSP.

Responsible for developing and implementing procurement strategies aligned with company objectives, managing solicitations and RFP lifecycle, negotiating vendor terms and pricing, tracking savings targets, maintaining market knowledge, building procurement capabilities, ensuring compliance in vendor selection and bidding, and managing staff. Requires bachelor's degree (or equivalent) and at least five years' experience in life-science procurement and outsourcing, with proficiency in Microsoft Office and strong negotiation and analytical skills.

Responsible for identifying opportunities and closing significant business for lab services including biobanking, sample preparation and specialty services; develops client relationships, writes proposals, creates project budgets/pricing, uses Salesforce, and represents the company at conferences/trade shows. Requires a relevant degree (Bachelors +5 years, Masters +2 years, or PhD +0-1 years) and experience selling to pharma/biotech/CRO customers. Salary range disclosed: $162,000—$243,000 USD/year.

Lead development of high-quality clinical study documents (protocols, IBs, ICFs, DSURs, CSRs, patient narratives) in compliance with Precision MW Style Guide, SOPs, ICH/FDA/GCP, and eCTD requirements. Responsibilities include document planning, authoring, editing/formatting, QC review, collaboration with sponsors/vendors, literature research, and process/SOP contribution. Requires a BS (or equivalent) in a scientific/medical discipline, proficiency with MS Office/Adobe/Teams, and 5+ years' relevant experience. Salary range disclosed: 101,800 - 152,600 (currency not specified).

Role involves negotiating and drafting commercial agreements (MSAs, consulting agreements, contractor agreements, NDAs, work/change orders), managing contract files and databases, ensuring compliance with company contracting standards, coordinating contract execution, tracking expirations/obligations, and escalating complex legal issues to corporate legal. Minimum 5 years' relevant experience; fluency in English required.

Precision For Medicine seeks a Senior Clinical Research Associate based in Argentina (remote) to independently manage complex clinical trial sites and monitoring activities (start-up, initiation, routine, close-out). Requires 5+ years as a CRA, strong site management experience, proficiency in English (professional), knowledge of ICH-GCP and local regulations, EDC/EHR experience, SAE handling, TMF/ISF management, and up to ~60% travel.

Responsible for building and maintaining financial and budgeting tools used by Business Operations, working with internal departments and external vendors (including ERP and Salesforce) to ensure reporting and functional requirements are met. Duties include implementing rates, training staff, supporting client-specific system adjustments, and participating in departmental initiatives. Minimum: Bachelor's degree and 5 years related experience; advanced Excel and VBA skills preferred.

The Business Development Director (Biospecimen Solutions) will identify, engage, develop, and close opportunities for biospecimen products and services (including biofluids, prospective collections, tissues, cells and central-lab offerings). Core duties include prospecting and qualifying leads, building and maintaining client relationship maps, retaining and growing accounts, cross-selling across the portfolio, resolving client issues through internal teams, maintaining Salesforce/CRM records, and attending conferences/trade shows. Minimum requirements: Bachelor’s degree in life sciences or related field and 1–2 years sales experience in life sciences/healthcare (or 3+ years laboratory research, service, clinical operations, or customer support). Role requires travel (up to 35%) and fluency in English. Compensation range provided: $162,000–$243,000 USD/year.

Lead site start-up strategy and execution for assigned country: develop activation readiness and critical path plans (IRB/EC & CA/MoH strategy, ICF customization, IMP release, contracts), coordinate stakeholders, track milestones and metrics, provide training and SME support, coordinate translations, and mentor less-experienced staff. Requires a bachelor's in life sciences or RN (or equivalent), experience in clinical start-up/CRO or pharma, and at least 2 years' experience in milestone/resource management. Fluency in English and the local language (Turkish) is required. Occasional travel may be required.

Remote role based in Hungary responsible for preparing and submitting clinical trial application dossiers to Competent Authorities and Ethics Committees, managing site activation readiness and timelines, coordinating translations and essential documents, supporting IMP release and contracts/budget negotiations, maintaining TMF and regulatory trackers, and acting as SME for local regulatory requirements and site start-up processes. Fluency in English required; relevant regulatory and start-up experience in CRO/pharma preferred.