Back to search.PPD Global - Senior Clinical Research Associate - Zagreb, Croatia
| Employment Type: | Permanent |
| Location: | Croatia, Zagreb |
| Salary: | Depending on Experience |
| Languages: | English, Danish, Dutch, French, German, Italian, Norwegian, Portuguese, Spanish, Swedish, Flemish, Greek |
| Required Languages: | 1 |
PPD is a leading global contract research organisation (CRO) providing discovery, development and post-approval services as well as compound partnering programmes. Our clients and partners include pharmaceutical, biotechnology, medical device, academic and government organisations.
Currently, we are looking for an experienced CRA with fluent English to enlarge by one our qualified team based in Zagreb, Croatia.
Description:
You will be primarily tasked to set up and monitor clinical trials conducted in Croatia as part of international projects. You should thrive in multi-national project teams, be focused on delivering exemplary levels of customer service, as well as:
* Conduct site visits to determine protocol and regulatory compliance
* Provide overall management of clinical operations resources
* Be responsible for the operational oversight and support for clinical studies: ensure that studies are planned and conducted efficiently and effectively, track study process, identify solutions proactively
* Critically review feasibility assessments and provide expert advice and alternatives to ensure studies are planned realistically and within given timelines
* Drive compliance to requirements necessary for clinical team to consistently gain success on the assigned projects
With a life sciences degree or nursing qualification and experience of Phase II to IV trials, you will have in depth knowledge of FDA and ICH GCP requirements.
Education and experience:
* Degree in Medical, Dental or Pharmaceutical Science
* Thorough working knowledge of drug development process, in particular monitoring and site management skills
* Extensive experience in clinical research industry including clinical monitoring
Requirements:
* In-depth knowledge of clinical development, Global Monitoring and Study Management processes, ICH-GCP, applicable legal and regulatory requirements
* Excellent organizational and negotiation skills
* Team player with the ability to work under own initiative
* Demonstrated skills to influence others and form strong cross-functional relationships
* Flexibility, proactiveness, critical assessment and good eye for detail
* Proven decision making skills
* Fluent English speaker (Any additional languages would be seen as a benefit)
* PC literate
Company offer:
We offer a chance to apply your knowledge on clinical research and have an insight of a fast growing multinational company. You will take advantage of our incentives for long-term relationship and competitive salary. You will benefit from the opportunity to obtain a managerial position in the near future.
PPD will only accept applications from candidates with the relevant language speaking skills alongside industry experience. Please do not apply if you do not fit the criteria.
PPD is an equal opportunities employer.
**PLEASE NOTE WHEN YOU CLICK APPLY YOU WILL BE REDIRECTED TO AN EXTERNAL URL / WEBSITE TO WHICH YOU HAVE TO SELECT CROATIA, CLICK ON EXPERIENCED CRA WITH MANAGERIAL FUNCTION JOB REF: 00106 AND APPLY ONLINE**
Currently, we are looking for an experienced CRA with fluent English to enlarge by one our qualified team based in Zagreb, Croatia.
Description:
You will be primarily tasked to set up and monitor clinical trials conducted in Croatia as part of international projects. You should thrive in multi-national project teams, be focused on delivering exemplary levels of customer service, as well as:
* Conduct site visits to determine protocol and regulatory compliance
* Provide overall management of clinical operations resources
* Be responsible for the operational oversight and support for clinical studies: ensure that studies are planned and conducted efficiently and effectively, track study process, identify solutions proactively
* Critically review feasibility assessments and provide expert advice and alternatives to ensure studies are planned realistically and within given timelines
* Drive compliance to requirements necessary for clinical team to consistently gain success on the assigned projects
With a life sciences degree or nursing qualification and experience of Phase II to IV trials, you will have in depth knowledge of FDA and ICH GCP requirements.
Education and experience:
* Degree in Medical, Dental or Pharmaceutical Science
* Thorough working knowledge of drug development process, in particular monitoring and site management skills
* Extensive experience in clinical research industry including clinical monitoring
Requirements:
* In-depth knowledge of clinical development, Global Monitoring and Study Management processes, ICH-GCP, applicable legal and regulatory requirements
* Excellent organizational and negotiation skills
* Team player with the ability to work under own initiative
* Demonstrated skills to influence others and form strong cross-functional relationships
* Flexibility, proactiveness, critical assessment and good eye for detail
* Proven decision making skills
* Fluent English speaker (Any additional languages would be seen as a benefit)
* PC literate
Company offer:
We offer a chance to apply your knowledge on clinical research and have an insight of a fast growing multinational company. You will take advantage of our incentives for long-term relationship and competitive salary. You will benefit from the opportunity to obtain a managerial position in the near future.
PPD will only accept applications from candidates with the relevant language speaking skills alongside industry experience. Please do not apply if you do not fit the criteria.
PPD is an equal opportunities employer.
**PLEASE NOTE WHEN YOU CLICK APPLY YOU WILL BE REDIRECTED TO AN EXTERNAL URL / WEBSITE TO WHICH YOU HAVE TO SELECT CROATIA, CLICK ON EXPERIENCED CRA WITH MANAGERIAL FUNCTION JOB REF: 00106 AND APPLY ONLINE**
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