Clinical research associate ii Vacatures

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

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