Job Openings for Senior Clinical Research Associate/CRA III Clinical Operations Asia at Bangalore, Karnataka

 

Novotech is internationally recognized as the leading independent and full service contract research organisation (CRO) in the Asia Pacific region. We provide a wide of  range clinical development services across all research phases and therapeutic areas; and have been instrumental in the success of hundreds of Phase I – IV clinical trials throughout the Asia Pacific.

Powered by the highest quality people, Novotech strives to set the benchmark for both business and clinical trial performance.

Our people are one of our key strengths. We value our people and recognize the work they do. We are lucky to have the best people and talent from across the Asia Pacific region work together to deliver to clinical trial success for our clients.

About the position:

Acting as the primary link between sites and sponsor, you will be responsible for:

• Acting as a site manager to ensure that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Novotech/Client SOPs;
• Providing mentorship to less experienced staff;
• Providing support to the project manager as required; and
• Performing site selection visits to ensure sites have adequate resources to conduct studies.

 

Minimum Qualifications & Experience:

• At least 3-4 years of independent Oncology experience;
• Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered);
• Solid knowledge of GCP, national and international regulations and a sound understanding of how they apply to you;
• Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments;
• Previous experience in monitoring oncology trials would be highly regarded; and
• A strong track record of performing visits to sites according to the Clinical Monitoring Plan
  

 

The Benefits

To achieve the highest standards in drug development, our people are 'best in class' and work tirelessly to develop better, safer and more effective therapeutics. In recognition of our people's commitment to quality and the skills they bring, Novotech rewards generously, offering competitive salary, attractive bonus potential and benefits tailored to meet a balanced lifestyle.

The Opportunities

We place a strong emphasis on a collaborative and collegiate work environment, giving you the opportunity to make a difference. We provide numerous opportunities to progress personally and professionally with scope to define your career path. Regular targeted internal and external training, as well as learning and knowledge-sharing opportunities, are an integral part of the development program for our valued staff.Novotech is internationally recognized as the leading independent and full service contract research organisation (CRO) in the Asia Pacific region. We provide a wide of  range clinical development services across all research phases and therapeutic areas; and have been instrumental in the success of hundreds of Phase I – IV clinical trials throughout the Asia Pacific.

Powered by the highest quality people, Novotech strives to set the benchmark for both business and clinical trial performance.

Our people are one of our key strengths. We value our people and recognize the work they do. We are lucky to have the best people and talent from across the Asia Pacific region work together to deliver to clinical trial success for our clients.

About the position:

Acting as the primary link between sites and sponsor, you will be responsible for:

• Acting as a site manager to ensure that clinical trials are conducted and documented as per ICH GCP guidelines, global and local regulatory requirements and Novotech/Client SOPs;
• Providing mentorship to less experienced staff;
• Providing support to the project manager as required; and
• Performing site selection visits to ensure sites have adequate resources to conduct studies.

 

Minimum Qualifications & Experience:

• At least 3-4 years of independent Oncology experience;
• Tertiary qualifications in clinical or life sciences related field (relevant experience/qualifications in similar professions may also be considered);
• Solid knowledge of GCP, national and international regulations and a sound understanding of how they apply to you;
• Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments;
• Previous experience in monitoring oncology trials would be highly regarded; and
• A strong track record of performing visits to sites according to the Clinical Monitoring Plan
  

 

The Benefits

To achieve the highest standards in drug development, our people are 'best in class' and work tirelessly to develop better, safer and more effective therapeutics. In recognition of our people's commitment to quality and the skills they bring, Novotech rewards generously, offering competitive salary, attractive bonus potential and benefits tailored to meet a balanced lifestyle.

The Opportunities

We place a strong emphasis on a collaborative and collegiate work environment, giving you the opportunity to make a difference. We provide numerous opportunities to progress personally and professionally with scope to define your career path. Regular targeted internal and external training, as well as learning and knowledge-sharing opportunities, are an integral part of the development program for our valued staff.

Link For this Job: https://novotech.bamboohr.com/jobs/view.php?id=607