Key responsibilities include:

• Visiting clients to communicate and provide feedback on drug information
• Organising product academic promotion activities

The goal is to meet comprehensive evaluation targets including professional skills, behaviour, compliance, and performance.

Pfizer is an equal opportunity employer and adheres to all relevant equal employment opportunity laws.

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Key responsibilities include:

• Providing timely and accurate professional support to customers within company policies and procedures
• Building partnerships with customers
• Planning and organizing academic meetings or activities
• Collecting market and customer feedback through company management systems and other compliant channels
• Analyzing and providing feedback and suggestions
• Maintaining effective communication with superiors, colleagues, and business partners from other departments
• Continuously improving professional knowledge and abilities

Requirements:

• University diploma in medicine, pharmacy, or related fields
• Proficient in MS Office, good English skills
• Strong communication and teamwork skills
• Ability to self-motivate and manage pressure
• Experience in the pharmaceutical industry is preferred

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation.

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As a Clinical Research Associate (CRA) I at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programmes.

Responsibilities

Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders. Key responsibilities include:

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON's procedures, protocols, and regulatory requirements.

Your Profile

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills. Required qualifications and experience:

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Job Data by YubHub.