Clinical Trial Manager assigned to client Mexico, Chile, Colombia, Brazil, Argentina

Há 4 dias


Brasil Syneos Health Tempo inteiro
Overview

Clinical Trial Manager assigned to client Mexico, Chile, Brazil, Argentina.

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you'll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives. Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE

Why Syneos Health

We are committed to developing our people through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people. We are continuously building the company we all want to work for and our customers want to work with. When we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we're able to create a place where everyone feels like they belong.

Responsibilities
  • Develop, coordinate, and implement Phase 1 clinical research studies at the organization's facilities, ensuring adherence to study protocols and timelines
  • Collaborate with the principal investigator to design study protocols and ensure scientific integrity
  • Liaise between research subjects, client teams, investigators, and clinic operations teams to facilitate smooth communication and coordination
  • Plan logistics and resource usage for clinical trials, including scheduling, staffing, and equipment needs
  • Track study progress in alignment with project milestones, client deliverables, and budget, and provide regular updates to stakeholders
  • Ensure compliance with applicable regulations globally and by region, including Good Clinical Practice (GCP) guidelines
  • Supervise experienced support employees and/or entry-level individual contributors, planning, prioritizing, and directing their tasks to ensure efficient workflow and high-quality output
  • Deliver operational results that have a moderate impact on the immediate achievement of results for the team, contributing to the overall success of the organization
  • Adapt new procedures, techniques, and tools to improve clinical trial processes and outcomes
  • Understand basic management approaches such as work scheduling, prioritizing, coaching, and process execution
Qualifications
  • Broad job knowledge in an operational, administrative, and/or specialized field
  • Practical knowledge in managing the execution of processes, projects, and tactics within a team
  • Understanding of the impact of work on related areas
  • This posting is intended for a possible upcoming opportunity rather than a live role. By expressing your interest, you\'ll be added to our talent pipeline and considered should this role become available.
Certifications
  • Relevant certifications in clinical trial management or related fields
Necessary Skills
  • Strong leadership and management skills
  • Excellent communication and collaboration abilities
  • Ability to plan and prioritize tasks effectively
  • Proficiency in tracking and reporting study progress
  • Knowledge of global and regional regulations for clinical trials
Core Focus
  • Supervising experienced support employees and/or entry-level individual contributors
  • Delivering operational results that have a moderate impact on the immediate achievement of results for the team
  • Utilizing broad job knowledge in an operational, administrative, and/or specialized field
  • Adapting new procedures, techniques, tools, etc. Understanding basic management approaches such as work scheduling, prioritizing, coaching, and process execution
Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Research, Analyst, and Information Technology
Industries
  • Biotechnology Research, Pharmaceutical Manufacturing, and Research Services

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