Serve as the primary clinical point of contact with clients, overseeing the operational portion of clinical studies per scope of work.
Develop study-related clinical documents, train CRAs and vendors, and lead internal clinical team meetings to ensure trial compliance.
Drive site feasibility, recruitment and retention strategies, and manage eTMF, budgets, and vendor oversight to ensure quality and timelines.
Precision for Medicine is a CRO that integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients, with a strong focus on Oncology and Rare Disease. The company combines new technologies, operational scale, and a collaborative environment to support the life sciences industry.
Manage all clinical aspects of assigned studies across multiple countries, ensuring timeline adherence and quality.
Lead CRAs and support site selection, start-up, enrolment, monitoring, data cleaning, and close-out.
Identify risks to timelines and collaborate with teams to deliver high client satisfaction.
Precision for Medicine is a precision medicine CRO combining novel trial designs, operational experts, and biomarker analytics with a focus on oncology and rare diseases. It encourages high-energy professionals who thrive in dynamic environments.
Lead Clinical Trial Liaison performance, development planning, and quality delivery across EMEA.
Oversee vendor-provided staff, implement standardised feasibility and site selection processes, and build investigator relationships.
Report monthly metrics, escalations, and best practices while retaining a 15% liaison workload.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, the company has a culture of innovation and has been recognized as a Great Place to Work.
Develop and lead enterprise-wide participant recruitment strategies to improve enrollment performance and accelerate study timelines across a multi-site clinical research network.
Drive participant funnel optimization, enrollment forecasting, and data-driven decision-making to enhance recruitment predictability and efficiency.
Spearhead cross-functional transformation roadmaps, platform adoption, and process improvement initiatives in partnership with Clinical Operations, Marketing, and Systems & Analytics.
Headlands Research is a network of next-generation clinical trial sites that integrates technology and high-quality support services to make clinical research accessible to participants. Founded in 2018, the company operates 20+ sites across the US and Canada and continues to grow its network and centralized capabilities.
Deliver end-to-end recruitment across Europe for clinical trial operations.
Source and engage candidates via LinkedIn, job boards, networking, and referrals.
Partner with hiring managers to ensure a positive candidate experience throughout the recruitment process.
PSI is a privately owned, full-service Contract Research Organization supporting clinical trials across the globe. With around 30 years of experience and an inclusive culture, PSI attracts top talent and fosters a collaborative environment.
Manage regulatory submissions and site activation readiness across the UK.
Negotiate budgets and contracts with sites and vendors.
Coordinate with ethics committees and competent authorities for approvals.
Precision for Medicine is a global Clinical Research Organization that combines novel clinical trial designs, operational and medical experts, advanced biomarker and data analytics, and a passion for rare diseases and oncology. The company values growth and innovation, fostering a collaborative and inclusive environment.
Serve as primary medical and scientific expert for clinical trial protocols and Expanded Access Programs.
Monitor trials to ensure participant safety, data accuracy, and protocol compliance.
Lead protocol development, investigator training, and cross-functional collaboration.
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, expanded access programs, and market access solutions. With 15+ years of experience across 150+ countries, they offer operational scale and a personalised culture.
Lead end-to-end delivery of Real-World Evidence studies in Germany and France, from contracting to final report.
Own project timelines, budgets, site coordination, and CRO oversight for reliable evidence.
Act as the sponsor's primary operational contact and align with Medical, Data, Legal, and Quality teams.
Resilience Care is a French company providing AI-driven remote monitoring for oncology, gastroenterology, and psychiatry. Founded in 2021, its solutions serve 35,000 patients across 200 facilities and an international, multidisciplinary team.
Lead planning, execution, and oversight of clinical studies across Latin America.
Act as primary client contact and ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
Mentor CRAs and partners while shaping country-level recruitment and monitoring strategies.
Precision Medicine Group provides clinical development, regulatory, and commercial solutions for life sciences companies. It fosters a collaborative, high-integrity culture with opportunities for growth and leadership in a global remote environment.
Serve as primary point-of-contact liaison with clients and oversee all aspects of clinical trials.
Manage study budgets, project timelines, risk, and cross-functional teams to ensure quality and compliance.
Drive bid defense preparation, client presentations, and continuous process improvement across assigned portfolios.
Precision for Medicine supports clinical research and development for biopharmaceutical and life science companies. It is a global, collaborative organization that emphasizes quality, innovation, and professional growth.
Support Rater Training Program and serve as liaison across teams
Manage study reporting and ensure timely deliverable completion
Mentor junior team members and lead small studies
Cogstate advances brain health by providing digital cognitive assessments used in clinical trials and healthcare settings. With a global team of experts, the company supports over 2,000 clinical trials across 150+ countries in a collaborative, patient-first culture.
Support the planning, coordination, and delivery of clinical research studies.
Collaborate with sponsors, cross-functional teams, vendors, and clinical sites to ensure studies meet timeline, budget, and quality targets.
Manage project milestones, site activation, patient recruitment, and risk mitigation in a remote working environment.
Jobgether is an AI-powered job matching platform connecting candidates with hiring companies. The hiring partner is a science-driven clinical research organization offering a collaborative remote environment.
Manage an assigned portfolio of clinical research technology customers, building trust and driving strategic account plans.
Lead onboarding, adoption, and training to help research sites maximize value from the clinical trial management platform.
Drive retention and revenue growth through renewals, expansion opportunities, and cross-functional collaboration.
This partner company provides innovative clinical trial management technology for healthcare and clinical research organizations. They foster a collaborative, inclusive, and technology-driven culture with multidisciplinary teams.
Complete coverage analysis tasks to support efficient clinical trial start-up for site clients.
Read and analyze clinical trial protocols and develop activity grids to identify required tests and assessments.
Interpret Medicare policies and billing guidelines to make determinations for clinical trial coverage.
WCG delivers transformational solutions that accelerate clinical research and advance human health. They invest in their people and foster a culture of growth and empowerment.
Lead clinical research project planning, execution, and delivery, ensuring regulatory compliance and quality.
Coordinate cross-functional teams and manage timelines, budgets, and study documentation.
Serve as the primary sponsor and client contact, providing regular project updates and resolving issues.
Alimentiv is a global CRO advancing therapies for gastrointestinal diseases, with deep expertise in IBD drug development. With about 700 employees across multiple countries, it is a private, profit-with-purpose company focused on scientific research and its people.
Conduct and report all types of onsite monitoring visits, including CRF review and source document verification.
Manage site communication and serve as the point of contact for in-house support services and vendors.
Support regulatory document preparation and participate in feasibility research for clinical studies.
We are a global CRO founded in 1995, working on the frontline of medical science to bring new medicines to patients. We bring together over 3000 dedicated professionals in a culture that cares for staff, clients, partners, and quality.
Lead research efforts on complex care cases, including reviewing medical records and clinical history.
Identify and evaluate diagnostic and treatment options, including clinical trials and innovative therapies.
Communicate research findings to clients and clinicians to support shared decision-making.
Private Health Management is a healthcare navigation firm that assists clients with serious and complex medical conditions. The company operates remotely across the United States with a team of compassionate, dedicated professionals focused on precision medicine.