Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms RSS Feed RSS Feeds RSS Feed PharmiWeb Candidate Blog RSS Feed PharmiWeb Client Blog

Job Details

Clinical Research Associate 2 with Oncology Experience

Company: Chiltern
Location: Remote - Anywhere in the USA
Reference: 137
Closing Date: 03 Nov 16
Type: Full Time
Salary (£): Competitive

Job Summary:

Looking for CRA's with Oncology experience located anywhere in the US-home based position. Chiltern is an EEO / AA Employer and is committed to providing opportunities to minorities, women, individuals with disabilities and veterans.




Positions can be either office-based or home-based, but work will be required away from Chiltern offices, at Sponsor offices, and may require national or international travel. May also involve travel to meetings or attendance at conferences. Overnight stays may be required. In addition weekend and evening sessions may be required depending upon the workload and nature of current programmes.


Clinical Monitoring Activities:

1. To prepare and conduct all site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and close-out visits according to relevant SOPs.

2. To identify potential centres for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required.

3. To ensure that investigator site files are assembled appropriately and that all required documentation is in place prior to release of clinical supplies

4. To be proactive in all dealings with study sites. To ensure that all study related communication including e-mail is tracked, printed and filed as required.

5. To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and LCRA.

6. To deal with local or central laboratories in order to ensure adherence to the protocol. To ensure that all relevant documentation is current e.g., accreditation certificates, normal ranges, etc.

7. To provide appropriate support for the preparation, submission/notification of local regulatory approval if required for local country requirements.

8. To distribute and track clinical trial supplies, e.g. CRFs, study medication, lab kits. To ensure that sites have sufficient supplies to continue recruitment.

9. To provide assistance in the production of Case Report Forms and protocol design.

10. To track CRFs collected during monitoring visits to data management.

11. To liaise with data management regarding data flow and data query processing.

12. To ensure that the interim safety reports are provided to EC/IRBs as per country requirements.

13. An understanding of the purpose of Chiltern's Clinical Project Management System (CPMS), how to use it, and how to navigate within the different sections. The ability to enter weekly details on Chiltern’s Project Management System.

14. To assist the Project Manager in the production of Status Reports.

15. To work in a timely manner in accordance with all the activities specified in the agreed study budget, under the supervision and guidance of the LCRA and Project Manager.

16. To raise invoice requests for investigator payments in accordance with Investigator/Hospital/Pharmacy agreement terms, to maintain the site financial tracking, producing a list for pending investigator payments and producing payment requests for Chiltern International as appropriate for local country requirements.

17. To facilitate translation and back translation of all necessary documents, as appropriate for local country requirements.

18. To be accountable for ensuring that all relevant study documentation is present for study sites.

19. To undertake other project related administrative tasks (i.e. meeting minutes, recruitment tracking, site file preparation) as appropriate, as assigned by the Project Manager and LCRA.

20. To document all study activities including investigator contacts using relevant forms.

21. To liaise with all other appropriate departments within Chiltern International to ensure the smooth running of the study.

22. To assemble files and ensure documents for the sponsor file accurately reflect the progress of the study.

23. Assist in the organization of meetings (investigator, sponsor, kick-off, face-to-face) and to present at the meetings.

24. To use all reasonable endeavours to work precisely according to schedules and timelines, established by the Sponsor and Project Manager for the conduct and completion of the study.


Job Requirements:

• A BSc or BA degree in a biomedical or related life science, or nursing qualification

• Previous CRA experience within clinical research of approximately 18 months

• Good clinical knowledge with an understanding of medical terminology

• An understanding of the basics of physiology and pharmacology

• Good computer literacy with working knowledge of PCs, Windows and Microsoft Office applications

• Good oral and written communication, organizational skills and personal presentation. The ability to communicate effectively in English.

• Experience working in a team environment under time and resource pressures

• Understanding of the principles of ICH GCP and regulatory requirements • Experience of the clinical research process and terminology

• Experience using a clinical trial management system


Key Attributes:

• Experience as a CRA on multicentre trials

• Positive outlook on the role of the Department and on Departmental or Company policy • Good understanding of the work performed by other Chiltern International functions and how they interact

1. Performance and Quality:

2. Conduct all activities according to the defined project-specific quality and performance standards as well as relevant SOPs, ICH/GCP, and local requirements.

3. Ensure awareness of project-specific quality and performance standards (within Clinical Monitoring Standards) and ensure that these are adequately documented, communicated and understood.

4. To be accompanied by Project Manager or Line Manager on selected visits (qualification, initiation, monitoring and close-out visits.)

5. To attend all relevant training and SOP training sessions.

6. Actively participate in training sessions and workshops. Provide training support for training sessions and workshops as required

7. Acknowledgement and acceptance to undergo continued training that may involve a variety of administrative tasks.

8. Ensure timely completion and documentation of all training requirements.


Apply for this job: Clinical Research Associate 2 with Oncology Experience

Contact Information:

Address:  Pennsylvania, USA
1016 W 9th Ave, King of Prussia, United States
PA 19406

Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.