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Clinical Research Associate 2(m/w/x)
Conducting site visits for clinical trials, supporting subject recruitment plans for medical treatments. Two years of on-site monitoring experience and GCP/ICH knowledge required. Company car, home-office, flexible schedules.
Requirements
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum two years of on-site monitoring experience or equivalent combination of education, training and experience
- Knowledge of clinical research regulatory requirements (GCP, ICH guidelines)
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in a fast-paced environment
- Flexibility for business travel (40-60%)
- Driver’s license class B
Tasks
- Conduct site selection visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions
- Monitor recruitment progress
- Oversee case report form (CRF) completion
- Track data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Provide subject matter expertise on specific topics
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Home-Office
- Flexible work schedules
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
Not a perfect match?
- IQVIA RDS GmbHFull-timeRemoteExperiencedFrankfurt am Main
- IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA MedTech
Clinical Research Associate 2(m/w/x)
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Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main
Clinical Research Associate 2(m/w/x)
Conducting site visits for clinical trials, supporting subject recruitment plans for medical treatments. Two years of on-site monitoring experience and GCP/ICH knowledge required. Company car, home-office, flexible schedules.
Requirements
- University Degree in life science or other scientific discipline or apprenticeship in the health care field
- Minimum two years of on-site monitoring experience or equivalent combination of education, training and experience
- Knowledge of clinical research regulatory requirements (GCP, ICH guidelines)
- Strong written and verbal communication skills
- Attention to detail
- Ability to work in a fast-paced environment
- Flexibility for business travel (40-60%)
- Driver’s license class B
Tasks
- Conduct site selection visits
- Conduct site initiation visits
- Conduct site monitoring visits
- Conduct site close-out visits
- Support the development of subject recruitment plans
- Evaluate site practices for quality and integrity
- Ensure compliance with GCP and ICH guidelines
- Track regulatory submissions
- Monitor recruitment progress
- Oversee case report form (CRF) completion
- Track data query resolution
- Collaborate with study site experts and client representatives
- Mentor less experienced team members
- Provide subject matter expertise on specific topics
Work Experience
- 2 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Benefits
Flexible Working
- Home-Office
- Flexible work schedules
Company Vehicle
- Company car
Other Benefits
- Accident insurance
Career Advancement
- Career growth resources
About the Company
IQVIA Biotech
Industry
Pharmaceuticals
Description
The company partners with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas.
Not a perfect match?
- IQVIA RDS GmbH
Clinical Research Associate 2 / CRA 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA
Clinical Research Associate 2 or Senior Clinical Research Associate 1(m/w/x)
Full-timeWith HomeofficeSeniorFrankfurt am Main - IQVIA MedTech
Clinical Research Associate 2(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main - IQVIA RDS GmbH
Experienced Clinical Research Associate, Multi-Sponsor(m/w/x)
Full-timeWith HomeofficeExperiencedFrankfurt am Main - ICON plc
Clinical Research Associate (CRA)(m/w/x)
Full-timeRemoteExperiencedFrankfurt am Main