Principal-level role responsible for leading the Clinical Science Analytics & Insights (CSAI) function across studies, including scientific review of clinical trial data, data cleaning and visualization, eCRF/EDC input and UAT, managing medical monitor reviews, and supporting cross-functional communication. Requires a minimum of 8 years clinical research experience, professional English, experience with EDC systems, and oncology/medical terminology expertise.

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.

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.

The Financial Analyst will support project teams across the life cycle of clinical trials, assisting with monthly invoicing worksheets, revenue recognition, variance and budget analysis, contract/change order review, and general ledger and financial close activities. Requires a bachelor’s in accounting/finance (or equivalent), a minimum of two years' relevant accounting and financial reporting experience, and strong Excel and communication skills.

Precision for Medicine is hiring a Site Contracts Manager to support European clinical studies remotely from Poland, Slovakia, Spain, Serbia, Romania or Hungary. Responsibilities include drafting, reviewing and negotiating CTAs, site contracts, vendor agreements and budgets; working with clinical operations and sponsors; tracking contract metrics; maintaining contract files; and improving contracting processes. Requires a 4-year degree and at least 5 years' relevant CRO/healthcare contracting experience.

Remote role (coverage specified for Poland, Slovakia, Spain, Serbia, Romania, Hungary). Reviews, drafts, negotiates and tracks clinical study agreements, site contracts, vendor agreements and confidentiality agreements; collaborates with clinical operations and stakeholders to ensure timely execution, maintains contract files and metrics, and supports process and policy improvements. Requires a degree and at least 5 years' CRO/healthcare contracting experience.

Role involves reviewing, drafting, negotiating and tracking site Clinical Trial Agreements, vendor and other client contracts; coordinating with Clinical Operations and study teams to meet timelines; maintaining contract files and metrics; and contributing to contracting policies and process improvements. Requires a 4-year degree and at least 5 years' relevant experience in CRO/healthcare contracting.

Precision for Medicine seeks a Site Contracts Manager to review, draft, negotiate and track clinical study agreements, vendor and consulting contracts, confidentiality agreements and site budgets. The role supports study teams, maintains contract files and metrics, and helps design contracting policies and processes. Requires a 4-year degree and at least 5 years' relevant CRO/healthcare experience in site CTAs, vendor contracts and budget negotiations; position can be covered remotely from Poland, Slovakia, Spain, Serbia, Romania or Hungary.

Responsible for drafting, reviewing and negotiating master services agreements, site contracts, CTAs, vendor and confidentiality agreements; working with clinical operations and sponsors to resolve contractual issues; tracking and reporting contract status and metrics; maintaining contract files and supporting policy/procedure implementation. Requires minimum 5 years' relevant CRO/healthcare contracting experience.

Precision for Medicine seeks a Site Contracts Manager (remote) to draft, review, negotiate and track CTAs, site contracts, vendor agreements and budgets; work with clinical operations and sponsors to meet study timelines; manage contract metrics, files and archiving; and help design contracting policies. Requires a 4-year degree and at least 5 years' relevant CRO/healthcare experience. Role can be based remotely from Poland, Slovakia, Spain, Serbia, Romania or Hungary.

The Senior Clinical Data Manager leads data management activities from study start-up to post-database lock for assigned clinical projects, including CRF specifications, database build and UAT, edit checks, query management, medical coding (MedDRA/WHODrug), SAE/AE reconciliation, TMF documentation, vendor coordination and team training. Requires 8+ years' experience, professional English, and experience with EDC systems (Medidata Rave, Veeva); occasional travel may be required.

Lead Data Management contact for assigned clinical studies: develop CRF specifications, oversee database build and UAT, define edit checks, perform/query data review and medical coding (MedDRA/WHODrug), manage TMF documentation, run study metrics and reporting, coordinate with sponsors/vendors, and provide training. Requires 8+ years' experience and professional English; experience with Medidata Rave and Veeva.

Lead development and optimization of clinical data systems and ETL pipelines; drive enterprise data standardization (CDISC), build validation frameworks, ensure regulatory compliance (GCP, FDA 21 CFR Part 11), develop dashboards and analytics, mentor junior engineers, and collaborate with Biostatistics, Clinical Operations, and Regulatory Affairs across LATAM.

Precision for Medicine seeks a Senior Clinical Research Associate (remote, based in central/southern Serbia) to monitor investigative sites in Bulgaria. The permanent role requires 3+ years of CRA experience, fluency in Serbian, English and Bulgarian, conduct and oversight of clinical studies per protocol, SOPs and ICH-GCP, study start-up activities, up to ~50-60% domestic travel (international travel may be required for some senior roles), and support/mentor junior staff.

Role focuses on increasing market awareness and customer base through inside sales activities: reviewing and improving account development processes, identifying prospects using Citeline/ZoomInfo/LinkedIn Sales Navigator, initiating outreach (calls, emails, direct mail), setting meetings for BD, recording activity in Salesforce/HubSpot, producing sales activity reports, mentoring inside sales team, and collaborating with Business Development leadership. Requires a bachelor's or equivalent, 5+ years in the CRO/pharmaceutical industry, full professional English proficiency, and availability for occasional domestic and international travel.