Accountable for day-to-day clinical study operations as primary clinical contact with clients and internal teams. Responsibilities include site feasibility and start-up, monitoring strategy and execution, eTMF/CTMS management, IP accountability, vendor oversight, CAPA implementation, and supporting audits. Minimum 7 years clinical research experience; role based in the United States (remote) with domestic and international travel expected.

Precision for Medicine seeks a Senior Clinical Research Associate to monitor and manage clinical studies (site setup, monitoring, regulatory activities) for oncology and rare disease trials. Requires fluency in English and German, experience as a CRA (minimum ~6 months), compliance with ICH-GCP, and availability for domestic travel (up to ~50-60%; some international travel possible for senior roles). Preferred experience includes CAR-T, FIH, phase III, study start-up and medical device exposure.

Review, draft, negotiate and track CDAs, CTAs, CTA-A amendments, vendor contracts and site budgets. Coordinate with internal study teams, sites and sponsors, maintain contract files/databases, and ensure contracting aligns with company policies and study timelines. Requires a bachelor’s degree or equivalent experience and at least 3 years of relevant contract experience in clinical research or a related industry.

Lead development and oversight of investigator grant and site budgets during proposals and clinical trials, manage grant administration (payments, reconciliations, reporting) globally for LATAM countries, and collaborate with Project Directors/Managers. Requires ≥5 years clinical research experience, ≥3 years leadership experience, strong financial/analytical skills and fluency in English.

Precision for Medicine is hiring a Senior Clinical Research Associate / Clinical Research Associate II to work fully home-based in the UK. The role involves monitoring and owning progress of clinical studies at investigative sites, ensuring conduct, recording, and reporting per protocol, SOPs and ICH-GCP, coordinating study setup activities (investigator identification, regulatory submission support, pre-study and initiation visits), identifying study risks and proposing mitigations. Candidates should have a 4-year degree (or equivalent) and ideally more than 1 year CRA experience; oncology and early phase experience are desirable. Fluency in English and availability for significant domestic travel (approximately 50–60%; international travel may be required for senior roles) are required.

Responsible for ensuring timely, inspection-ready Trial Master Files across LATAM studies: create and execute TMF Plans and Indexes, manage document review and processing, perform/oversee periodic quality reviews, monitor TMF health/metrics, support audits and inspections, manage study close-out and eTMF handover. Requires a bachelor's degree (or equivalent), a minimum of 3 years related experience, professional working proficiency in English, experience with eTMF systems, and knowledge of ICH-GCP/FDA guidance.

Responsible for serving as the primary clinical lead for studies covering the China market, including site feasibility and start-up, CRA oversight, eTMF and CTMS management, regulatory/IRB submissions, IP accountability, metric reporting, and implementation of CAPAs. Requires coordinating with cross-functional teams, supporting investigator meetings, and ensuring data quality and compliance.

The role owns procurement activities supporting clinical trials, including RFP lifecycle management, negotiating supplier terms/pricing, vendor contracting, and ensuring compliance with purchasing processes. Requires a Bachelor's degree, at least 2 years of life science procurement/outsourcing experience, strong negotiation and communication skills, and proficiency with Microsoft Office. Candidates must be legally authorized to work in the country of employment without employer sponsorship.

Seeking a Senior CRA based in Argentina (remote) to independently manage complex clinical trial site activities including start-up, initiation, routine monitoring, close-out, ISF/TMF reconciliation, EDC/EHR data review, SAE handling, IP management, audit readiness, and mentoring junior staff. Requires a 4-year scientific/healthcare degree, at least 5 years as a CRA in CRO or pharma/biotech, professional-level English, and ability to travel (up to ~60%).

Precision seeks a Start Up Specialist to prepare clinical trial application dossiers and submissions to Competent Authorities and Ethics Committees, coordinate site activation/IMP release, support contract and budget negotiation, maintain project trackers and TMF, and liaise with cross-functional teams. Candidates located in Hungary, Poland, Serbia, Slovakia or Romania with fluency in Hungarian (and English) are eligible; applicants must be legally authorized to work in the country of employment without employer sponsorship.

The Financial Analyst provides financial support across the project lifecycle for clinical trials, including preparation of monthly invoicing worksheets, variance analysis, review of work/change orders, and collaboration on financial reporting and month/quarter/year-end close. Requires a Bachelor's in Accounting/Finance (or equivalent), a minimum of two years' general ledger and financial reporting experience, strong Excel skills and familiarity with project budgets, EVA and contract review.

The Manager, Account Development will drive market awareness, generate leads, and expand the customer base through inside sales activities (calls, email, direct mail), account and territory strategies, and CRM usage (Salesforce, HubSpot). Role requires a minimum of 5 years in the CRO/pharmaceutical industry, knowledge of oncology and rare disease development markets, and full professional proficiency in English. Occasional domestic and international travel is required.