Cardiovascular Clincal Research Coordinator- West Coast/Midwest

We are an incubator/management firm focused on the medical technology, biotechnology, and healthcare fields. The Company?s principals have extensive experience in these fields as founders, early stage investors, major shareholders, and executives in the medical device and healthcare industries.  The unifying principle underlying these fields is the Company?s ability to leverage the medical and technical knowledge and experience of the people involved in its various ventures.  We have 9 portfolio companies in the US within our group at different stages of development. 

We are currently in search of a Cardiovascular Clinical Research Coordinator

for one of our portfolio companies.  The company specializes in implantable medical devices for congestive heart failure.  The Cardiovascular Clinical Research Coordinator responsibilities will include the following:

 Become fully aware of the details of each research protocol. 

 Manage patient identification, recruitment, and retention for the clinical research protocol.  This will require detailed chart review of potential patient records, discussing patients with their physicians and the sponsor representatives,

 Travel between various practices and hospitals covered by the trial. 

 Communicate with study physicians and other personnel on a daily basis regarding scheduling of patients, progress of studies, and problems as they develop and take direction from the PI?s at the sites.

 Abstract data from patient medical records for completion of source documentation and eCRFs. 

 Complete weekly and monthly reports as needed.

 Conduct research activities including basic assessment of patients' status, obtain vitals (blood pressure, pulse, weight, height), medical/medication history, ECG, shipment of tests to core laboratory, patient education, teaching and instruction, follow-up, and schedule patient visits.

 Establish and maintain a professional working relationship with study subjects, physicians, and other office personnel.

 Complete and maintain copies of all study records and original documentation.

 Assist in preparation and presentation for sponsor FDA site visits / audits.  Assist in tracking study device supplies and appropriate accountability records, and storage.

 Willingness and desire to learn computer skills including word processing, excel spreadsheets and electronic data entry.

 

 

Some required qualifications include:

 RN or Science Degree preferred.

 Clinical trial experience and 2 years experience preferred in cardiovascular arena.

 Excellent organization skills and independent decision making to ensure smooth function of the clinical tasks is essential.

 Must have aptitude for technical problem solving and the skills required for independent scientific research.

 Must have excellent verbal, written and interpersonal skills.

 Familiarity with simple computer programs is desirable.

 Ability to function independently with in a fast-paced, changing environment, develop timelines and meet deadlines.

 Ability to handle confidential information and comply with GCP and HIPPA regulations at all times

 

The position is field based on the West Coast, Midwest or East Coast.

If you are interested please forward an updated resume with salary requirements to resumes@almyrainc.com .

Agency calls will not be accepted.