Clinical research associate cra oncology Vacatures

Over de vacature

Overview

In this role you will monitor clinical studies at investigative sites to ensure trial activities align with protocol, SOPs, and ICH-GCP. Based in Belgium or the Netherlands with remote work and regular site travel, you will support oncology trials and contribute to high-quality data and outcomes. You will coordinate study setup and monitoring activities, from investigator identification to regulatory submissions and initiation visits. You join a smaller CRO culture that emphasizes impact, collaboration, and work-life balance, with direct support from line management.

Verantwoordelijkheden

• Monitor progress of clinical studies at investigative sites to ensure conduct, recording and reporting per protocol, SOPs, ICH-GCP, and applicable regulations
• Coordinate study setup and monitoring activities (identify investigators, regulatory submissions, pre-study and initiation visits)
• Ensure study quality and timely issue mitigation through proactive risk identification and collaboration with study team
• Communicate with investigators and cross-functional teams to keep projects on track

Belangrijkste vereisten

• 2+ years as a CRA in CRO or pharmaceutical/biotech industry or equivalent

• Experience managing oncology studies

• Life science degree or equivalent

• Fluency in English and Dutch; French a plus

• Availability for 50-60% travel (domestic; international for some roles)

• Excellent communication and organizational skills; client-focused approach

• Team player and able to handle conflicts using standard resolutions

• calm and thoughtful under pressure

• proactive problem-solving

• detail-oriented

• oncology study monitoring

• site management

• regulatory submissions

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities

Over de vacature

Overview

As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You'll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.

Arbeidsvoorwaarden / Benefits

• remote-based position
• reasonable travel
• supportive management
• focus on work-life balance
• high CRA retention culture

Verantwoordelijkheden

• Monitor and own progress of clinical studies at investigative sites
• Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
• Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)

Belangrijkste vereisten

• Life science degree and/or equivalent experience

• 2+ years as CRA in a CRO or pharma/biotech setting or equivalent

• Experience managing oncology studies

• Site management or similar clinical research experience

• Excellent communication and organizational skills; team player; client-focused

• Fluency in English and Dutch; French a plus

• Availability for domestic travel up to 50-60% (international travel may be required)

• calm, thoughtful, and responsive under pressure

• proactive problem solving

• attention to detail

• ICH-GCP compliance

• SOPs and regulatory submissions

• study start-up activities