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Responsibilities
The Clinical Trial Manager (CTM) provides operational expertise and leadership to multiple clinical trial teams, to ensure the effective and efficient delivery of all aspects of multiple studies, through all phases of clinical study management, ndard Operating Procedures (SOPs), conventions and instructions, as well as current Good Clinical Practice (GCP), International Conference on Harmonization (ICH), and applicable local regulations.Make an Impact at Veristat!Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.105+ approved therapies for marketing applications prepared by Veristat480+ oncology projects in the past 5 years350+ rare disease projects delivered in the past 5 yearsFlexible, inclusive culture — 70% remote workforce, 66% women-led teamsLearn more about our core values here !What we offer:The estimated hiring range for this role is $150K – 160K plus applicable bonus. This hiring range is specific to the USA and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.Benefits vary by location and may include:Remote workingFlexible time offPaid holidaysMedical insuranceTuition reimbursementRetirement plansWhat we look forBachelor’s Degree required; degrees in health sciences strongly preferred5 or more years of experience as a CRA in a CRO or Pharmaceutical setting, and ability to effectively lead a project team requiredThorough knowledge of clinical operations, clinical development process, and ICH/GCP and regulatory environment requiredAbility to serve as a mentor, coach and trainer for assigned CRAsExcellent oral and written communication skills luding proficient presentation skills required to effectively support and manage exchanges with external customers; ability to speak and write in other languages a plusProficient knowledge of study specific therapeutic area to enable appropriate input to study documents (e.g., protocols, CRFs, EDC development)Proficiency d, Excel, and PowerPoint requiredProficiency in, and ability to learn new, clinical systems including EDC, IVRS, CTMS, eTMF and other clinical project management tools requiredAbility to self-motivate, be a team player, and work independentlyExcellent critical thinking and problem-solving skills requiredAbility to self-motivate, work collaboratively within a team, proactively manage workload, and manage competing priorities in a fast-paced environment requiredAutomated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.
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