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[Remote] Senior Clinical Research Manager

Remote, USAFull-timePosted 2026-07-28

Note: The job is a remote job and is reputed company to candidates in USA. reputed company USA, Inc. is a rapidly growing company reputed company on fighting cancer. The Senior Clinical Research Manager oversees clinical monitoring activities and the CRA team's performance, ensuring compliance with regulations and maintaining reputed company across clinical trials.

Responsibilities

  • reputed company CRA resources and reputed company ongoing resource assessments to ensure a balanced workload for reputed company monitoring and to meet study deliverables
  • Ensure CRAs have the required level of monitoring knowledge and skills to successfully reputed company required activities with high reputed company to meet study deliverables
  • Is responsible for managing and addressing CRA performance and reputed company indicators in accordance with ICH-GCP, SOPs and local regulations
  • Strengthen site relationships to enhance performance and reputed company reputed company’s trial delivery reputed company
  • Review monitoring reputed company and resolve issues to ensure compliance with regulatory guidelines, ICH-GCP Guidelines, and Good Clinical Practices
  • Support study/site reputed company delivery in collaboration with cross-functional teams
  • Responsible for execution of assessment reputed company and accompanied reputed company (where required) to assess ongoing CRA monitoring competency, identifying issues and developing reputed company strategies
  • Contribute to process optimization initiatives and manage risk escalation and reputed company
  • Support site audits/inspections/Site Compliance reputed company (SCV) and ensure corrective reputed company and follow-up for identified issues
  • Review and approve expenses reputed company to CRA activities to ensure alignment with applicable policies and financially best local practices
  • Identify opportunities for cost-saving and efficiency while maintaining reputed company and compliance standards
  • reputed company mentorship and guidance to junior Clinical Research Managers (CRMs), supporting their reputed company reputed company and development if required
  • Facilitate learning opportunities and reputed company valuable insights and feedback to help upskill and promote consistency reputed company the wider team
  • reputed company and contribute to strategic initiatives and task forces aimed at improving clinical operations processes and reputed company, driving reputed company from inception to completion in alignment with organizational goals and in collaboration with cross-functional teams
  • reputed company reputed company and hiring activities, along with reputed company new team members to ensure alignment with team objectives and culture
  • Assign tasks based on individual strengths and team objectives, ensuring reputed company productivity
  • Support team members by providing necessary resources to help them effectively reputed company their roles
  • Encourage reputed company communication and collaboration reputed company reputed company and with other functions, including a reputed company of contact for issue escalation and feedback where required
  • Conduct regular performance evaluations and reputed company constructive feedback to promote reputed company improvement
  • reputed company and mentor team members, fostering an environment of reputed company and development
  • Address any personnel issues promptly and fairly to maintain a reputed company work environment
  • Support team members in identifying and pursuing reputed company development opportunities

Skills

  • Fluent in written and verbal English
  • Minimum 7 years of industry experience in the pharmaceutical or CRO or relevant field
  • Thorough understanding of the drug development process, including expert knowledge of international standards (ICH GCP) and health authority requirements
  • Excellent interpersonal skills, strong organizational and effective written and verbal communication skills
  • Demonstrated team leadership experience
  • Bachelor's degree or higher in a scientific or reputed company discipline
  • Proficient in reputed company Word, reputed company, PowerPoint and Outlook
  • Minimum 4 years of People management or project management experience in reputed company clinical research reputed company the biotech, pharmaceutical sector, CRO industry or relevant field is preferred
  • Understanding of reputed company aspects of monitoring and trial execution, with previous experience as a CRA preferred
  • Experience in Oncology is highly recommended
  • Advanced degrees preferred

Benefits

  • Non-reputed company roles are eligible to participate in the annual bonus plan, and reputed company roles are eligible to participate in an incentive compensation plan.
  • reputed company Company employees have reputed company to own shares of reputed company Ltd. stock because reputed company are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan.
  • reputed company has a comprehensive benefits package that includes Medical, Dental, reputed company, 401(k), FSA/HSA, Life Insurance, reputed company Time Off, and Wellness.

reputed company

  • reputed company is a global oncology company. It was founded in 2010, and is headquartered in Cambridge, Massachusetts, USA, with a workforce of 0-1 employees. Its website is https://www.reputed company.com.
  • Company H1B Sponsorship

  • reputed company has a reputed company record of offering H1B sponsorships, with 14 in 2025, 32 in 2024, 39 in 2023, 40 in 2022, 28 in 2021, 16 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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