Project Manager II (Sponsor dedicated)

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Project Manager II (Sponsor dedicated) based in Brazil.

Join a global clinical research environment where you will lead complex studies and help accelerate the delivery of innovative healthcare solutions. This role combines project leadership, stakeholder management, and clinical research expertise to ensure successful study execution from launch through closeout. You will collaborate with multidisciplinary teams, sponsors, and research partners while maintaining high standards of quality, compliance, and operational excellence. The position offers the opportunity to manage impactful clinical programs while working with experienced professionals across the healthcare industry. You will play a key role in improving processes, mitigating risks, and ensuring research projects meet strategic goals. This is an ideal opportunity for a clinical research professional with strong project management skills and a passion for advancing patient-focused solutions.

Accountabilities:: Lead and manage interdisciplinary clinical research projects, ensuring delivery according to timelines, budgets, quality standards, and contractual requirements.

Act as the primary point of contact between project stakeholders and sponsors, supporting successful study initiation, execution, and completion.

Ensure all assigned studies comply with Good Clinical Practice (GCP), applicable regulations, standard operating procedures, and quality expectations.

Coordinate project teams, study partners, and operational activities while proactively identifying and resolving risks or issues.

Manage project financial performance, tracking budgets and supporting efficient resource allocation.

Oversee project plans, study milestones, deliverables, and documentation requirements, including Trial Master File (TMF) quality and completeness.

Maintain accurate study information across project management systems and databases.

Support inspection readiness activities and ensure operational processes meet regulatory standards.

Prepare and present project updates, reports, and status information for internal and external meetings.

Develop risk mitigation strategies and contingency plans to support successful study outcomes.

Build strong relationships with stakeholders to support future collaboration opportunities.

Participate in business development activities, including bid defense meetings when required.

Provide guidance and leadership to project management team members or clinical monitoring staff when applicable.

Requirements:

Bachelor’s degree or equivalent qualification in life sciences, medicine, pharmacy, nursing, or a related field.

Minimum of 5 years of experience in clinical research, including previous project management experience.

Experience working within a clinical research organization (CRO) environment is preferred.

Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and relevant regulatory requirements.

Experience managing clinical studies, project timelines, budgets, and cross-functional teams.

Strong organizational skills with the ability to manage multiple priorities independently.

Excellent communication, presentation, and interpersonal skills in both written and spoken formats.

Ability to develop strong relationships with clients, sponsors, and internal teams.

Direct therapeutic area experience is preferred.

Ability to adapt to new technologies and digital tools used in clinical research.

Willingness and ability to travel as needed, approximately 25%.

Benefits:

Fully remote work opportunity from Brazil.

Opportunity to manage international clinical research projects with global impact.

Career development and progression opportunities.

Access to technical and therapeutic area training.

Supportive management and professional growth environment.

Recognition programs and comprehensive rewards initiatives.

Opportunity to collaborate with multidisciplinary experts in healthcare and life sciences.

Exposure to innovative technologies, research methodologies, and global healthcare initiatives.

Inclusive workplace culture focused on collaboration and personal development.

How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best!  Why Apply Through Jobgether?    Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.     #LI-CL1