Clinical Project Specialist assigned to client Home Based Mexico

Syneos Health; México; Presencial; MXN 748.222 - 1.122.334; Jornada completa

Descripción de la vacante

A global biopharmaceutical solutions organization is seeking a Clinical Project Specialist based in Mexico. This role involves planning and overseeing clinical trials, ensuring regulatory compliance, managing project timelines, and collaborating with cross-functional teams. The ideal candidate has a strong background in clinical project management with at least 3 years of experience and excellent organizational skills.

Formación

• Minimum of 3 years of experience in clinical project management or related field.
• Strong understanding of clinical trial processes and regulations.
• Experience with SOP, GCP, and country-specific regulations.

Responsabilidades

• Planning, directing, creating, and communicating clinical study timelines.
• Gathering input from cross-functional teams for comprehensive plans.
• Overseeing and resolving operational aspects of clinical trials.
• Selecting sites and vendors, negotiating contracts, and managing relationships.
• Preparing clinical trial budgets and monitoring expenditures.

Conocimientos

Excellent organizational and time management skills

Strong communication and interpersonal skills

Ability to work effectively in a team environment

Proficiency in Microsoft Office Suite

Attention to detail and problem-solving skills

Ability to adapt to changing priorities

Educación

Associate's degree or higher in a related field

Herramientas

Microsoft Office Suite

Descripción del empleo

Overview

Clinical Project Specialist assigned to client Home Based Mexico. Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model centers the customer and the patient, with a focus on simplifying and streamlining work. You will collaborate with cross-functional teams to help our customers achieve their goals in either Functional Service Provider partnerships or Full-Service environments.

We are a global team of problem solvers driving the delivery of therapies and improving lives. WORK HERE MATTERS EVERYWHERE

Responsibilities

• Planning, directing, creating, and communicating clinical study timelines, ensuring milestones are met and the project stays on track
• Gathering input from cross-functional teams (clinical, regulatory, data management) to create comprehensive plans for timely deliverables
• Standardizing procedures to ensure consistency of clinical study processes across trials
• Overseeing and resolving operational aspects of clinical trials, ensuring activities comply with SOPs, GCP, and country-specific regulations
• Selecting sites and vendors, negotiating contracts, and managing relationships to ensure high-quality and timely delivery of services
• Preparing clinical trial budgets and monitoring expenditures to keep studies within budget
• Monitoring trial progress, tracking KPIs, and following up with team members and line managers to address deviations
• Implementing and aligning the clinical development strategy with overall project goals
• Developing trial recruitment strategies, identifying target populations, creating recruitment materials, and monitoring enrollment progress

Qualifications

• High school diploma or equivalent required
• Associate's degree or higher in a related field preferred
• Minimum of 3 years of experience in clinical project management or related field
• Strong understanding of clinical trial processes and regulations
• Experience with SOP, GCP, and country-specific regulations

Certifications

• Certification in Clinical Project Management or related field preferred
• Good Clinical Practice (GCP) certification preferred

Necessary Skills

• Excellent organizational and time management skills
• Strong communication and interpersonal skills
• Ability to work effectively in a team environment
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
• Attention to detail and problem-solving skills
• Ability to adapt to changing priorities and work under pressure

Additional Information

Summary: Roles within Clinical Project Management at the S11 level are responsible for planning, directing, creating, and communicating clinical study timelines, gathering input from cross-functional teams, ensuring consistency of processes, overseeing operational aspects, adhering to SOP/GCP and country regulations, site/vendor selection, budget preparation, and monitoring progress. These roles may implement the clinical development strategy and develop trial recruitment strategies to support the clinical development program.

We are committed to compliance with applicable laws and equality directives and provide reasonable accommodations when appropriate during the recruitment and employment process.