Id: 165877 Location: Philadelphia, PA Job Type: Contract Sr. Oncology Clinical Research Associate - In-House and Monitoring
Our client, a leading Oncology company is looking for multiple North East CRAs based on long-term contract opportunities located in Philadelphia, PA. We are looking for a CRA who can help with the office workload as well as go out on local (North East Region) monitoring assignments.
Oncology experience (5+ years) to fill multiple Oncology CRA roles. Hourly rate (W2, 1099, C2C) is opened for discussion ***Please only apply when you have previous Oncology/Hematology experience***
***Please forward your resume (word document) directly to firstname.lastname@example.org or call Rose Chu at 610-822-1256 for questions***
In-house CRA tasks and minimum monitoring services within North East region
Assist PM, Senior PM, Assistant PM, and CRAs on projects and activities - performing all duties in accordance with Good Clinical Practices, the organization's SOPs, Sponsor's SOPs and FDA Regulations.
Serves as a liaison between sites to facilitate communication. Conduct routine site management for duration for studies. Senior position will manage and oversee investigational sites
Perform regulator review and tracking of documentation
Interfaces with investigators, IRB's, and company personnel.
Perform regulatory review and perform tracking of documentation.
Perform Case Report Form collection and or solicitation. Review submitted data and monitoring trip reports. Oversee clinical study compliance.
Complete site tracking reports and site contact documentation reports as required by study.
Please respond directly to Global Employment Solutions, Inc. with your resume attached - WORD document.
Requirements: *** Must have 4+ years Oncology trial experience, SOCRA/ACRP is preferred ***
A Bachelor's Degree from an accredited college/university or a graduate of an accredited nursing school. SOCRA certification is a plus.
8+ year pharmaceutical industry CRA experience , along with 5 years of Oncology (solid and liquid tumors) research .
Prior project management experience in Industry-sponsored, multi-site sponsored, and Cancer Cooperative Group is encouraged.
Must have strong interpersonal and communication skills; and must demonstrate self-direction, organization and problem-solving abilities.
25% travel required, some work will be performed in-house in Center City Philadelphia.
Search Terms: CRA, In-House CRA, Junior Clinical Research Associate, Oncology PM, Oncology CPM, Oncology Clinical Project Manager, Oncology Project Manager, Regional CRA, CRA Monitor, Sr. Clinical Project Manager, CCRP, Oncology Trials, development of Oncology Studies, implementation of Oncology Studies, management of Oncology Studies, completion of oncology clinical studies, bid proposals, SOP Writing, project development, NIH, pharmaceutical sponsors/ funders, investigators, Study Manager, Cancer Cooperative, SOCRA/ACRP, GCP, SOPs, Clinical Operations Manager, Clinical Trials Manager, Clinical Trial Manager, Clinical Research Manager, Clinical Operation Manager, Sr. Clinical Operations Manager, Project Management
We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the stated requirements. To protect our client's interests, we will not be responding to inquiries that do not contain a CV/Resume. Finally, please include the position ID (rc- Sr. Oncology CRA ) in the subject line of your correspondence to ensure review. Please forward your credentials in Word format, in confidence, to: Rose Chu at email@example.com or call Rose Chu at 610-822-1256 for discussion.
Vice President - Pharmaceutical, CRO, Biotech, Medical Device
Global Employment Solutions/Fahrenheit IT
P (610)822-1256 | C (215)-317-2999 | F (610-668-5000) | firstname.lastname@example.org
One Presidential Blvd. North, Suite 310, Bala Cynwyd, PA 19004
We're looking for hot talent! Tell your friends and get $250 plus a new iPad 2, iPad Mini, Apple Sport Watch or iPod Touch. Sign up!