2 559 Posti di lavoro per Cra, Italy in Italia
Cra, Italy
Lavoro visualizzato
Descrizione Del Lavoro
***
**Responsibilities**:
- Gather and evaluate site necessary documents and guarantee site regulatory files are accomplished and precise.
- Supervise site compliance with IRB policies/procedures and assure reporting, proposals and approvals in a timely manner.
- You will track and report progression of study, data supervising, protocol variations, issue resolution, and follow up compliance.
- Plan and accomplish visit trip reports, confirmation and follow up letters in timelines defined in the CMP.
- Evaluate research specimen sample documentation, storage and processing, and guarantee shipments are sent to central lab when needed.
- Other duties may be assigned to this role.
**Key Skills and Requirements**:
- Educated to a degree level or at least 1-2 years of experience in pertinent work and training.
- Past involvement in oncology would be ideal, and in a supervisory role.
- Know-how of and capable of implementing CFR and GCP/ICH.
- Familiarity within international clinical trials.
- Computer literacy.
- An organised individual with the ability to manage own time efficiently.
- Capable of handling various tasks simultaneously with the ability to take own initiative.
- Able to prioritise workload with a high attention to detail.
- Interpersonal and communication skills both verbally and in writing.
- Willing to travel for business needs up to 60-80% of the time.
- Works well in a team.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
LI-GE1
CRODelivery
Clinical
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Tuttavia, di seguito sono disponibili lavori simili per te.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
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Informazioni sulle ultime novità Cra, italy Posti di lavoro;/Posti Vacanti nella Italia !
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.
CRA - Italy
Ieri
Lavoro visualizzato
Descrizione Del Lavoro
At CliniRx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We’re looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research.
What You’ll Do:
- Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans.
- Conduct site initiation, monitoring, and closeout visits, ensuring all activities comply with SOPs and regulatory requirements.
- Perform Source Document Verification (SDV), review ICFs, oversee eCRF completion, and ensure SAE reporting accuracy.
- Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards.
- Support sites with training, essential document collection, and audit/inspection readiness.
- Identify and engage potential new sites across therapeutic areas.
Who You’ll Work With:
You’ll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery.
What Success Looks Like:
- High-quality and timely site monitoring
- Accurate and compliant documentation
- Strong site engagement and smooth study execution
What We’re Looking For
- Graduate/Postgraduate in Life Sciences
- 1–4 years of experience in site monitoring
- Strong knowledge of ICH GCP and clinical trial regulations
- Excellent communication, multitasking, and problem-solving skills
Location: 100% Remote (Home-Based)
At CliniRx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you’re ready to contribute to impactful clinical research and grow with a collaborative team, apply now.