Source Job

Global

  • We welcome professionals from a variety of backgrounds and experience levels within clinical research.
  • We look for those passionate about Clinical Operations, Site Enablement & Site Management, and Clinical Business Development Functions.
  • We also welcome professionals from Regulatory & Compliance, Feasibility & Patient Recruitment, and Patient Access & Healthcare Innovation.

20 jobs similar to Join Our Global Talent Community

Jobs ranked by similarity.

APAC

  • Assist in the coordination and management of clinical trials, including study start-up, maintenance, and close-out activities.
  • Support Clinical Trial Managers in overseeing CRO deliverables, timelines, issue escalation, and overall study operational performance.
  • Maintain, organize, and update essential study documentation to ensure they are complete, accurate, and audit-ready at all times.

Bicara Therapeutics is a clinical-stage biotech company pioneering bifunctional antibodies for targeted tumor modulation. Founded in 2020, they've built a global team of over 100 employees headquartered in Boston, with a focus on advancing their lead asset. We encourage people from all backgrounds to apply and cultivate a culture where all voices are included.

US

  • Plan, lead, and manage clinical trials, developing comprehensive project plans for timelines, budgets, and deliverables.
  • Ensure regulatory compliance by working with the Compliance Team and preparing for audits, adhering to GCP guidelines and company SOPs.
  • Serve as a primary communication point for sponsors and internal teams, providing regular updates and building client relationships for future business.

Paradigm Health is a company rebuilding the clinical research ecosystem by enabling equitable patient access to trials and enhancing trial efficiency. The team, backed by leading investors like ARCH Venture Partners, is multidisciplinary and committed to creating equitable access to clinical trials for any patient, anywhere.

Australia

  • Manage and motivate a team of CRAs to achieve Precision for Medicine’s quality standards.
  • Support the career development of the organization’s Clinical Research Associate (CRA) workforce.
  • Strengthen the quality and productivity of operations within the group.

Precision for Medicine is a Clinical Research Organization with a uniquely integrated offering. They combine novel clinical trial designs, industry-leading operational and medical experts, and advanced biomarker and data analytics solutions.

$130,000–$150,000/yr
US 4w PTO

  • Partner with Clinical Operations leadership to support clinical trial execution.
  • Lead site feasibility, selection, initiation, and greenlight activities for clinical trial sites.
  • Provide guidance and oversight to CRAs, including trip report review and training support.

Immatics is dedicated to making a significant difference in the lives of cancer patients. They are a global frontrunner in precision targeting of PRAME, found in over 50 cancers, with cutting-edge science and a strong clinical pipeline.

US

  • Serve as the primary operational lead for assigned studies.
  • Partner with sponsors and CROs as a key point of contact.
  • Proactively identify operational risks, including enrollment challenges and protocol-related issues.

M3 Wake Research is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations. With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US.

US

  • Provide operational oversight and support for multiple clinical research sites within the network.
  • Ensure adherence to GCP, FDA regulations, ICH guidelines, HIPAA, and sponsor protocols.
  • Build and maintain strong working relationships with Sponsors, CROs, and external partners.

Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. They leverage convenient, trusted healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs.

US

  • Independently coordinate assigned study activities in compliance with protocols, SOPs, GCP, and regulatory requirements.
  • Manage scheduling and execution of virtual and home-based study visits, assessments, and follow-up activities.
  • Serve as a primary point of contact for research participants and caregivers, including Spanish-speaking populations

Synapticure provides instant access to expert neurologists, cutting-edge treatments and trials, and wraparound care coordination and behavioral health support in all 50 states through a virtual care platform. As a patient and caregiver-founded company, Synapticure is dedicated to transforming the lives of millions of individuals and their families living with neurodegenerative diseases.

Europe

  • Serve as the primary post-sale partner, building trusted, strategic relationships.
  • Lead onboarding and training, monitor account health, and deliver regular business reviews.
  • Identify process improvements, strengthen internal workflows, and influence customer success strategy

Mural Health aims to make clinical trials easier for participants and caregivers by removing obstacles. They seem to be a startup, with a culture of collaboration and cross-functional teamwork.

Canada US

  • Develop client-ready deliverables such as study protocols, statistical analysis plans, and technical reports for health technology assessment submissions.
  • Manage project components by collaborating with team members to ensure timely delivery, financial performance, and high-quality outputs, while handling day-to-day client communications.
  • Provide mentorship and direction to junior researchers, contribute to business development proposals, and apply technical expertise in systematic reviews and indirect treatment comparisons like NMA and MAIC.

Precision Medicine Group is a global portfolio organization specializing in evidence synthesis for health technology assessments in the pharmaceutical industry. The company has a culture similar to a start-up, is well-funded, and prides itself on being a visionary leader in its field.

$220,000–$270,000/yr
US

  • Leads Patient marketing strategies for COMP360, inclusive of digital/media efforts and patient support materials.
  • Partners with Commercial Operations, Sales Leadership, and Medical Affairs to drive Patient awareness.
  • Owns creation of marketing materials that educate Patients and Care Partners on COMP360's value proposition.

Compass Pathways plc is a biotechnology company dedicated to accelerating patient access to evidence-based innovation in mental health. The Company is headquartered in London, UK, with offices in New York City in the US and focuses on developing novel treatments that have the potential to improve the lives of those who are suffering with mental health conditions.

Singapore South Korea

  • Develop, mentor, manage and coach SSU personnel to ensure quality standards.
  • Ensure SSU personnel work to the highest quality standards and maintain compliance.
  • Participate in the interview process for new SSU personnel by conducting CV review.

Precision for Medicine is a Clinical Research Organization with an integrated offering enabling the science of precision medicine. They combine clinical trial designs, operational and medical experts, biomarker and data analytics solutions, with a passion for rare diseases and oncology.

Europe

  • Develop and negotiate global study budgets based on the requirements of a study protocol.
  • Review, draft and negotiate a variety of agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements.
  • Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.

Precision Medicine Group is a specialized services company supporting life sciences organizations. We don't have information about the company's size, culture or number of employees from the job posting.

US

  • Oversees all aspects of study site management to ensure patient safety and data quality.
  • Independently conducts all forms of site visits and prepares monitoring reports.
  • Communicates effectively with site personnel and Precision Project and Clinical Trial Management.

Precision Medicine Group is a company that works in clinical research. They are an equal opportunity employer that values diversity and inclusion.

Global

  • Guide and develop a remote team of researchers responsible for identifying and maintaining global healthcare reference data while ensuring compliance and quality standards.
  • Design data production processes and drive improvements in both process and technology, fully owning team performance metrics for efficiency and quality.
  • Collaborate with engineering teams on automation, escalate risks early, and thrive in a fast-paced, multi-cultural remote environment requiring strong leadership and operational skills.

Veeva Systems is a mission-driven pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As a fast-growing public benefit corporation with over $3B in revenue, it fosters a culture of speed, customer success, and employee success in a flexible, Work Anywhere environment.

Mexico

  • Lead and scale agile project management practices.
  • Collaborate with cross-functional teams to improve project outcomes.
  • Develop and implement project strategies to enhance efficiency.

Konovo is a global healthcare intelligence company with a mission to transform research through technology, enabling faster, better, connected insights. With over 300 employees across 5 countries, they collaborate to support some of the most prominent names in healthcare.

$102,000–$120,000/yr

  • Supports all phases of clinical development and execution.
  • Ensures high quality data by being the study protocol expert and key site resource for questions.
  • Maintains and tracks clinical study data and supports investigator qualification selection.

SI-BONE is a medical device company focused on minimally invasive sacropelvic solutions. They aim to help patients with sacroiliac pelvic conditions and have provided over 90,000 procedures to date using their iFuse Implant System.

$125,000–$175,000/yr
US

  • Lead day-to-day data management activities for assigned clinical trials.
  • Oversee CRO and vendor data management deliverables to ensure timelines, quality, and compliance.
  • Ensure data integrity, consistency, and completeness through ongoing data review and cleaning.

Faeth Therapeutics is a clinical-stage oncology company advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program. They are a small, focused team where every person has direct impact and are united by a shared commitment to care deeply, create boldly, and never stop learning.

Europe

  • Identify and target potential healthcare facilities in the UK market.
  • Build strong relationships with clients, understanding their staffing needs.
  • Present the benefits of Greenstaff Complex Care interim nursing contracts.

ICG Medical is a global healthcare recruiter focusing on nurses, midwives, and home care/healthcare workers with a vision to improve patient care. The company has offices in the UK, Ireland, India, South Africa, China, Philippines, Australia, Canada, and the USA.

Mexico

  • Lead and coach Senior Project Managers to deliver high-quality qualitative research at speed.
  • Translate client objectives into clear qualitative research plans and actionable execution strategies.
  • Build and maintain a culture of client-first execution and continuous improvement.

Konovo is a global healthcare intelligence company on a mission to transform research through technology- enabling faster, better, connected insights. With over 300 employees across 5 countries, we collaborate to support some of the most prominent names in healthcare.

US

  • Develop, execute, monitor, and adapt strategic MSL stakeholder engagement plans.
  • Lead high-quality scientific exchange through both proactive and reactive interactions.
  • Identify and communicate insights, trends, and activities of other Medical Affairs organizations.

They focus on engaging key opinion leaders (KOLs) and healthcare providers in high-quality scientific exchange. They drive insight generation and contribute to the development and execution of medical strategy.