Clinical Research Specialist
Clinical Research Specialist
5 months with a possibility to extend
Medtronic – Santa Rosa, CA
Duties:
- Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.
- Assist in preparation of study materials and/or training.
- Interface with, and assure training of investigators, site staff, and Medtronic clinical staff.
- Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).
- May arrange conference calls, staff meetings and training events.
- Assist data management group with review of clinical data/information and oversight of data correction.
- May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).
- Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.
- Contribute to ongoing SOP development and review.
- Participate in training to enhance knowledge base.
- Must be willing to assist with other duties as needed such as filing and document tracking.
- Must have ability to prioritize and critical thinking skills and previous clinical research experience.
- Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy.
Qualifications
Top 3 qualifications:
- Previous clinical research experience
- Ability to prioritize and strong critical thinking skills
- Attention to detail and strong communication skills
Additional Information
All your information will be kept confidential according to EEO guidelines.
IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT 619-727-5167 ASAP! I want to know more about your preferences.
If in case you know someone who might be interested for this, feel free to pass it along. I look forward to hearing from you!