Icon Job Openings for Multiple Positions - Apply Now!

Icon Job Openings for Multiple Positions – Apply Now!

Icon plc, a leading global provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology, and medical device industries, is offering exciting job opportunities across various positions. If you’re looking for a dynamic career in the healthcare industry, these roles could be the perfect fit for you. Explore the following job openings and take the next step in your professional journey.

Job Openings

Site Management Associate
EVO CRA I
Regulatory Publishing Specialist
CRA II
Clinical Research Associate II
Medical Director – Hemato-Oncology
CRA I

Site Management Associate

Job Description

We are seeking a Site Management Associate who will be responsible for site management activities to ensure compliance with protocols and regulatory requirements. This role involves working closely with clinical research teams to oversee study sites and maintain quality standards.

Key Responsibilities

Manage and monitor clinical trial sites
Ensure adherence to protocols and regulatory guidelines
Collaborate with clinical research associates and investigators
Conduct site visits and assessments
Maintain accurate documentation and records

Qualifications

Bachelor’s degree in Life Sciences or related field
Previous experience in site management or clinical research
Strong organizational and communication skills
Ability to work independently and in a team environment
Knowledge of GCP and regulatory requirements

How to Apply

To apply for the Site Management Associate position, please visit our careers page and submit your application.

EVO CRA I

Job Description

The EVO CRA I will support the planning and execution of clinical trials by monitoring and managing site activities. This entry-level position provides an excellent opportunity to gain experience in clinical research.

Key Responsibilities

Conduct site monitoring visits
Ensure compliance with study protocols and regulatory standards
Assist in the management of study sites
Collect and review study data
Communicate with site staff and clinical teams

Qualifications

Bachelor’s degree in a related field
Strong interest in clinical research
Excellent attention to detail and organizational skills
Good communication and interpersonal skills
Basic understanding of clinical trial processes

How to Apply

To apply for the EVO CRA I position, please visit our careers page and submit your application.

Regulatory Publishing Specialist

Job Description

We are looking for a Regulatory Publishing Specialist to join our regulatory affairs team. This role involves preparing and managing regulatory submissions to ensure compliance with global regulatory requirements.

Key Responsibilities

Prepare and format regulatory submissions
Ensure accuracy and completeness of submission documents
Manage submission timelines and deliverables
Collaborate with regulatory affairs and clinical teams
Stay updated on regulatory guidelines and changes

Qualifications

Bachelor’s degree in Life Sciences, Regulatory Affairs, or related field
Experience in regulatory publishing or submissions
Proficiency in electronic submission software
Strong attention to detail and organizational skills
Knowledge of global regulatory requirements

How to Apply

To apply for the Regulatory Publishing Specialist position, please visit our careers page and submit your application.

CRA II

Job Description

The CRA II will play a crucial role in the management and monitoring of clinical trials, ensuring compliance with protocols and regulatory requirements. This mid-level position requires experience in clinical research and site management.

Key Responsibilities

Monitor clinical trial sites and ensure protocol adherence
Conduct site visits and assessments
Review and verify clinical data
Collaborate with investigators and site staff
Prepare and maintain study documentation

Qualifications

Bachelor’s degree in Life Sciences or related field
Minimum of 2 years of experience in clinical research
Strong knowledge of GCP and regulatory requirements
Excellent communication and organizational skills
Ability to travel and manage multiple sites

How to Apply

To apply for the CRA II position, please visit our careers page and submit your application.

Clinical Research Associate II

Job Description

We are seeking a Clinical Research Associate II who will be responsible for monitoring clinical trials and ensuring compliance with regulatory standards. This position involves working closely with investigators and site staff to support clinical research activities.

Key Responsibilities

Conduct site monitoring visits
Ensure adherence to study protocols and regulatory guidelines
Review and verify clinical data
Collaborate with clinical research teams and site staff
Maintain accurate study documentation

Qualifications

Bachelor’s degree in Life Sciences or related field
Minimum of 2 years of experience in clinical research
Strong knowledge of GCP and regulatory requirements
Excellent communication and organizational skills
Ability to travel and manage multiple sites

Medical Director – Hemato-Oncology

Job Description

We are looking for a Medical Director – Hemato-Oncology to lead our oncology clinical trials and provide medical expertise. This senior-level position requires extensive experience in oncology and clinical research.

Key Responsibilities

Lead and oversee oncology clinical trials
Provide medical expertise and guidance to clinical teams
Ensure compliance with regulatory requirements
Collaborate with investigators and key opinion leaders
Develop and review clinical trial protocols

Qualifications

Medical degree (MD or equivalent)
Extensive experience in oncology clinical trials
Strong knowledge of regulatory requirements and clinical research
Excellent leadership and communication skills
Ability to work in a fast-paced, dynamic environment

How to Apply

To apply for the Medical Director – Hemato-Oncology position, please visit our careers page and submit your application.

CRA I

Job Description

The CRA I will support the monitoring and management of clinical trial sites. This entry-level position provides an opportunity to gain valuable experience in clinical research and site management.