The LSAD is responsible for leading Local Study Team(s) at country level to ensure timely delivery of clinical study commitments per ICH-GCP and client procedures. Duties include site identification/qualification, monitoring oversight, CTMS/eTMF management, regulatory and ethics submissions, budgeting and payments, risk management, and supporting audits/inspections. Role requires oncology experience, minimum 3 years in development operations or related fields, proficiency in English, a relevant bachelor's degree, and ability to travel nationally and internationally.

The Local Study Associate Director (LSAD) leads Local Study Team(s) at country level to ensure timely delivery of clinical study commitments to required quality. Responsibilities include site identification/qualification, monitoring and oversight from activation through closure, management of CTMS and eTMF, regulatory and ethics submissions, budgeting and payments, risk management, patient recruitment support, and preparing for audits/inspections. Minimum 3 years' relevant experience and proficiency in English plus fluency in local language(s) are required.

The Local Study Associate Director leads Local Study Team(s) at country level (Brazil) to deliver clinical study commitments according to timelines and quality standards. Responsibilities include site identification/qualification/monitoring, CTMS and eTMF management, regulatory and IRB/EC submissions, budgeting and agreements, risk management, and coordination with global stakeholders. Minimum 3 years' relevant experience required; proficiency in English and fluency in local language(s) required.

The Local Study Associate Director (LSAD) is responsible for country-level delivery of clinical study commitments, leading CRAs/CSAs, overseeing site selection, initiation, monitoring and closure, maintaining CTMS/eTMF, coordinating regulatory/EC/IRB submissions, managing budgets and risks, and supporting patient recruitment. Requires minimum 3 years' related experience and proficiency in written and spoken English; fluency in local language(s) is also required.

Parexel is hiring a Local Study Associate Director (LSAD) based in Poland (100% remote). The role is dedicated to a single client and involves country-level responsibility for delivering clinical study components according to timelines, budget and applicable guidelines (ICH-GCP and local regulations). Key tasks include study budgeting (fSMA), preparing MICFs/ICFs and translations, EC/IRB and regulatory submissions, site start-up oversight, and leading local study teams. Minimum requirement: 5 years trial management experience, including oncology and site monitoring experience. Base pay range listed: PLN 300,000–320,000 per year.

Role involves leading the site contracting lifecycle (strategy, execution, monitoring, risk mitigation), mentoring a site contracts team, collaborating with sponsors, CROs and internal stakeholders, managing budgets and forecasting, and developing project setup documents. Requires 3–5 years' experience in site contracting within the CRO industry and a bachelor's degree or equivalent.

Parexel FSP is hiring a Senior Clinical Research Associate based in Spain (remote). The role involves independent site monitoring, study set-up and oversight, preparing protocol/consent/regulatory/ethics (IRB) submissions, and completing study documentation and status reports. Requires a bachelor's in life sciences, a minimum of 5 years' independent site monitoring experience (≥2 years in oncology), ICH GCP knowledge, ability to travel ~65–75% (domestic and international), and a current driver's license.

Parexel is hiring a home-based Senior CRA in Poland to manage and monitor oncology studies for a single client. The role includes full site management and supervisory responsibilities, mentoring junior CRAs, working with study teams and technology, and opportunities to travel. Requirements include extensive site management experience, minimum 5 years of independent site monitoring and at least 2 years as a CRA in oncology. Base pay range for Poland is PLN 230,000–260,000 and benefits include car or car allowance, medical (health, dental & vision) plan, and life assurance.

Parexel FSP is hiring a Senior Clinical Research Associate (home-based, Israel) to be dedicated to a single client and manage all site management and supervisory activities for assigned oncology studies. The role expects extensive site management experience, at least 2 years' oncology CRA experience and a minimum of 5 years' experience in independent supervision of visits. Responsibilities include mentoring junior CRAs, working with clinical trial technology, and supporting study conduct in accordance with GCP/ICH and applicable legislation. The posting mentions premium salary and benefits (car or company car, medical care plan including health/dental/vision, life assurance) and opportunities to travel.

Accountable for global execution of site activation and country start-up strategy for assigned studies, including CRO/vendor management, TMF/CTMS documentation, regulatory submissions support, metrics tracking, risk mitigation, and ensuring compliance with ICH-GCP. Role may require up to 25% travel and asks for 4–6 years of experience.

Parexel seeks a Local Study Associate Director (100% remote, Spain) to lead country-level clinical operations for a single client under FSP. Responsibilities include delivering study components per timelines and budget, preparing and maintaining study budgets/fSMAs, leading local study teams, preparing MICFs/ICFs and translations, and managing EC/RA submissions. Requires minimum 5 years trial management experience, local experience with SSU oversight, site monitoring experience, oncology trial experience, and knowledge of ICH-GCP and local clinical research regulations.

Parexel is recruiting a Country Operations Manager accountable for set-up, execution and delivery of assigned clinical trials at the country level. Responsibilities include ensuring compliance with GCP-ICH and local regulations, CRO and vendor oversight, budget creation and management, site feasibility and selection, patient recruitment planning, training, monitoring oversight, risk mitigation, and reporting. The role requires a minimum of 5 years' clinical trial management experience; oncology study experience and vendor/CRO management experience are preferred. The position is fully home-based and limited to candidates living in Germany.

Parexel is pre-recruiting for a Local/Country Trial Manager based in Germany (fully remote). Accountable for operational and scientific oversight, trial set-up, execution and delivery at the country level, including oversight of CROs and vendors, budget management, feasibility and site selection, recruitment planning, risk mitigation, compliance with GCP/ICH and local regulations, and contribution to patient-facing materials. Minimum 5 years' clinical trial management experience; oncology experience preferred.

Parexel FSP is hiring multiple Clinical Research Associates and Senior Clinical Research Associates (Mexico - remote). Roles include site selection/start-up, initiation, monitoring (remote and on-site), SDV/SDR, CRF review, eTMF and CTMS updates, drug accountability, SAE reporting, and inspection/audit support. Requirements include a related Bachelor's degree, ICH-GCP knowledge, local language fluency and proficiency in English; experience: 1+ years for CRA and 3+ years for Senior CRA. Travel nationally/internationally as required.

Parexel FSP is hiring multiple Clinical Research Associates and Senior Clinical Research Associates to manage site selection, initiation, monitoring (onsite and remote), and closure for clinical studies. Responsibilities include SDV/SDR, CRF review, CTMS and eTMF updates, drug accountability, SAE reporting, regulatory/EC/IRB submissions, investigator training, and ensuring inspection readiness. Requirements include proficiency in English, fluency in the local language (Portuguese), a related bachelor’s degree, and 1+ years CRA experience (or 3+ years for Senior CRA). Travel nationally/internationally as required.

On-site and remote monitoring role responsible for site initiation, monitoring, and closure; ensuring compliance with ICH-GCP and local regulations; managing study and drug supplies; performing SDV/SDR and CRF review; updating CTMS/eTMF; supporting audits/inspections. Requires English proficiency, fluency in local language(s), relevant degree, and 1+ years (CRA) or 3+ years (Senior CRA) of on-site CRA experience.

Hudl seeks a Lead Engineer to autonomously own a core camera platform system (automatic capture, device connectivity, video pipelines, fleet management). The role requires experience with distributed systems, software that interfaces with physical devices/IoT, operational ownership (incident response, monitoring, runbooks), and mentoring engineers. Tech stack and experience mentions include .NET Core, Python, MongoDB/DocDB, Redis, RabbitMQ, AWS IoT Core, and video technologies such as GStreamer, HLS, or WebRTC. Role is based in the United States (remote candidates accepted; preference for proximity to Lincoln, NE).

Lead and grow the global Apromore sales organization (Regional VPs and AEs) to drive ACV bookings, manage sales forecasting and funnel metrics, and maintain key customer relationships. Requires 8+ years in software/applications sales, leadership experience recruiting and developing sales teams, and preferred experience with process intelligence/AI-driven and cloud enterprise solutions. Degree or equivalent experience required.

The Serials Sales Manager (Serials Specialist) is a U.S.-based remote role focused on serials and subscription management for EBSCO's SSD portfolio in the Western US. Responsibilities include partnerships with Regional Sales Managers, owning renewals strategy, developing account growth and retention plans, managing a sales pipeline and CRM reporting, and collaborating with Account Services, Operations, and publisher partners. The role requires 7+ years relevant experience and up to 60% travel.

Lead technical architect for Coinbase's Risk Platform responsible for designing and implementing high-throughput, low-latency, highly available backend systems (real-time fraud detection, risk decisioning, financial risk monitoring), shaping multi-quarter technical strategy, collaborating with Data Science/ML/Product/Compliance, and mentoring engineers. Requires 8+ years backend experience and experience with microservices, event-driven architectures, REST/GraphQL, and building systems at scale.