Senior ICF Medical Writing Project Manager

Thermo Fisher Scientific Inc.; Ciudad de México; Presencial; USD 60,000 - 100,000; Jornada completa

Descripción de la vacante

An innovative organization is seeking a Senior ICF Medical Writing Project Manager to lead critical initiatives in clinical research. This role involves ensuring the delivery of high-quality Informed Consent Forms and compliance with regulatory standards. The successful candidate will develop project timelines, collaborate with diverse teams, and resolve client management issues. With a focus on integrity and innovation, this position offers a dynamic work environment and opportunities for professional growth. Join a forward-thinking company committed to improving health and safety globally.

Servicios

Competitive Remuneration

Annual Incentive Plan Bonus

Healthcare

Employee Benefits

Career Development Prospects

Innovative Company Culture

Formación

• 5 years experience in project management in a scientific or medical field.
• Experience in managing medical writing or clinical projects.

Responsabilidades

• Develop project timelines, standards, budgets, and forecasts.
• Collaborate with cross-functional teams to meet deliverables.
• Monitor timelines and provide status updates.

Conocimientos

Project Management

Planning and Organizational Skills

Interpersonal Skills

Communication Skills

Problem-Solving Abilities

Decision-Making Abilities

Educación

BS/BA in a Scientific Field

Advanced Degree

Descripción del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety.

We have a vacancy for a Senior ICF Medical Writing Project Manager based in Mexico.

Discover Impactful Work:

Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance.

A day in the Life:

• Develop project timelines, standards, budgets, and forecasts.
• Collaborate with cross-functional teams to meet deliverables.
• Monitor timelines and provide status updates.
• Identify and resolve client management issues.
• Ensure compliance with quality processes.

Keys to Success:

• Proven project management skills.
• Strong planning and organizational abilities.
• Excellent interpersonal and communication skills.
• Ability to work independently and under pressure.

Education

• Prefer BS/BA in a scientific field with 5 years experience, or an advanced degree with 3 years experience.

Experience

• Experience managing medical writing or clinical projects.
• Pharmaceutical/CRO industry experience preferred.
• Advantageous to have experience in regulatory and/or plain language medical writing.

Knowledge, Skills, Abilities

• Solid project management, budgeting, and forecasting skills.
• Effective problem-solving and decision-making abilities.
• Proficient in global and regional regulatory guidelines.

Physical Requirements / Work Environment

• Office-based role with exposure to electrical office equipment.
• Occasional travel to client sites; domestic and rare international travel.
• Frequent stationary periods, hand movements, and light lifting (15-20 lbs).

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!