Description:

• Serves as the primary CRC for a portfolio of clinical research studies that may involve industry sponsored Phase I, II, III and IV clinical trials, drug, biologic, device, government-funded clinical research, and investigator-initiated clinical research. • Ensures compliance with the Code of Federal Regulations and Good Clinical Practice guidelines to ensure smooth, accurate progress of studies from the planning and approval stages through study completion and post-study closure. • Works with the PI to manage the day-to-day activities of the study including problem solving, internal and external communication and protocol management. • Responsible for screening, recruitment and retention of study participants. • Responsible for developing source documents and accuracy of protocol data abstracted from medical records and other sources. • Identify, document, and assist with Institutional Review Board (IRB) mandated reporting. • Develop and ensure compliant processes with study protocols. • Provide expertise in the planning, development and budgeting for clinical trials. • Provide guidance and support of team members and newer research staff as a point person and reliable source of information. • Supports leadership in process improvement projects, standard operations policies and new initiatives as a subject matter expert in clinical research.

Skills:

Clinical research, cardiology, Pre-screening patients, Chart review, Patient recruitment, Edc, Crc

Top Skills Details:

Clinical research,cardiology

Additional Skills & Qualifications:

• Minimum of 2+ years clinical research experience or a combination of research and clinical experience to equal 5+ years. (cardiovascular experience in a clinical setting preferred) • Strong interpersonal, written, and verbal communication skills with a history of working collaboratively as part of a team • Strong attention to detail, demonstrated critical thinking, problem solving and decision-making abilities • Ability to handle multiple priorities and be results oriented • Proficiency in MS Office, Outlook, and knowledge of Excel functionality • Experience working in an electronic medical record systems e.g., Epic Preferred Qualifications: • Certified Clinical Research Coordinator/Professional (CCRC or CCRP) certification strongly preferred

Experience Level:

Intermediate Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.