Precision for Medicine is hiring a Senior Clinical Research Associate based in Turkey (fully home based possible). The role includes monitoring and owning clinical study progress at investigative sites, ensuring compliance with protocol/SOPs/ICH-GCP, coordinating study set-up activities, conducting pre-study/initiation visits, supporting larger trials, mentoring junior staff, and interacting with clients. Required: university degree in a life science/health discipline, 3.5+ years CRA experience, significant site management and oncology monitoring experience, and fluency in English and Turkish. Travel up to ~60% and international travel as needed.

Lead Contracts Manager role supporting regional expansion (Mexico, Brazil, Argentina, Colombia, Chile, Peru). Responsibilities include drafting, reviewing, negotiating, and tracking master services agreements, site CTAs, vendor agreements and budgets; managing contract metrics and files; coordinating with Clinical Operations and study teams to meet timelines. Minimum 5 years' relevant experience and a graduate/4-year degree.

The Contracts & Budgets Associate develops and negotiates regional and global study budgets, reviews/drafts/negotiates confidentiality and clinical study agreements, coordinates execution and contract filing, and works with clinical operations and stakeholders to resolve contractual issues. Requires a bachelor’s degree or equivalent experience and a minimum of 1 year of relevant clinical research contract experience.

Responsible for conducting feasibility analyses (pre-award and post-award), site and country analysis, recruitment and epidemiology analysis, protocol review, and site outreach. Requires a bachelor’s in life sciences, minimum 5 years' related experience, professional-level English, knowledge of ICH-GCP, and proficiency with MS Office and web/data platforms. Role supports business development and study delivery across oncology and rare disease projects.

Join the Feasibility Department to deliver pre-award and post-award feasibility projects, site identification and enrollment modelling. Responsibilities include feasibility analyses (competitive, epidemiology, recruitment), protocol review, site outreach, presenting findings to BD/clients, and engaging with stakeholders including patient advocacy groups. Requires a Bachelor's in life sciences (or equivalent), minimum 5 years relevant experience, professional-level English; postgraduate degree preferred.

The Senior Feasibility Associate/Feasibility Manager will deliver pre- and post-award feasibility analyses (including recruitment, epidemiology, protocol and site/country assessments), undertake site outreach and identification, support enrollment modelling and collaborate with BD, clients, sites and partners. Requires a life sciences bachelor’s degree, minimum 5 years' relevant experience, professional English, strong data/IT and presentation skills, and knowledge of ICH-GCP. Role may be performed remotely in the listed European countries.

Responsible for conducting feasibility analyses, site and country assessments, site identification and outreach, recruitment and enrollment modelling, and presenting findings to business development and clients. Requires a life sciences bachelor's degree, a minimum of 5 years' related experience, professional-level English, and experience with data platforms and MS Office; ICH-GCP knowledge is expected.

Responsible for delivering feasibility deliverables including pre-award RFP input, protocol and assumptions review, site and country analysis, recruitment/enrollment modelling, site identification and outreach, and presenting feasibility recommendations to BD/clients. Requires a life sciences bachelor's degree and a minimum of 5 years' related experience; English professional proficiency and knowledge of ICH-GCP. Role can be covered remotely in the UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

Responsible for conducting feasibility analyses (competitive, recruitment, epidemiology, protocol review), site identification and outreach, enrollment modelling, and presenting recommendations to business development and clients. Requires a bachelor’s in life sciences, minimum 5 years' relevant experience, strong data/IT skills, and professional-level English. Knowledge of ICH-GCP and experience with oncology/rare disease trials preferred.

Role responsible for conducting feasibility analyses (pre- and post-award), site and country analysis, protocol review, recruitment and epidemiology analysis, site outreach, and enrollment modelling. Requires a bachelor's in life sciences (or equivalent), minimum 5 years' related experience, professional-level English, strong data/IT skills and familiarity with ICH-GCP. Remote in UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.

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.

Lead and oversee global clinical project management for autoimmune programs, providing strategic oversight, resource allocation, risk management, and governance for clinical study projects. Requires a minimum of 10 years' clinical research experience, working knowledge of GCP/ICH, people management experience, ability to travel domestically and internationally; salary range disclosed at $162,000–$243,000 USD per year.

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.

Remote Senior Clinical Data Engineer (LATAM) responsible for enterprise-level data standardization and mapping, designing validation frameworks, building modular pipelines and databases, ensuring regulatory compliance (GCP, FDA 21 CFR Part 11), developing dashboards and analytics, and collaborating with Biostatistics, Clinical Operations, and Regulatory Affairs. Requires minimum 6 years' relevant experience and proficiency with Python, R, SQL, and SAS.