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Precision for Medicine is not your typical CRO. At Precision for Medicine we have brought together new technologies, expertise and operational scale to help the life sciences improve the speed, cost and success rate of bringing life-changing therapies to patients. What sets us apart is the way we integrate clinical trial execution with deep scientific knowledge, laboratory expertise and advanced data sciences.
We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will focus on an average of one to two studies setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result.
Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
About you:
How we will keep you busy and support your growth:
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Senior CRAs handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope. You will also have the opportunity to train and mentor junior staff members. You will interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.
Qualifications:
Minimum Required:
Other Required:
Preferred:
We invite you to learn more about our growing organization serving our clients that are researching ground breaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Full Time
Business Services
$53k-69k (estimate)
01/20/2023
09/06/2023
precisionmedicinegrp.com
BETHESDA, MD
50 - 100
2012
MARIA BRONSHTEIN
$5M - $10M
Business Services
The job skills required for Clinical Research Associate (Italy) include Clinical Trial, SOP, Oncology, Commitment, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Associate (Italy). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Associate (Italy). Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Research Associate (Italy) positions, which can be used as a reference in future career path planning. As a Clinical Research Associate (Italy), it can be promoted into senior positions as a Scientist - Clinical Research that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Associate (Italy). You can explore the career advancement for a Clinical Research Associate (Italy) below and select your interested title to get hiring information.