Senior Clinical Research Coordinator

Job Title: Clinical Research CoordinatorJob Description

We are seeking an experienced Clinical Research Coordinator who will oversee the day-to-day activities of clinical trials in accordance with Good Clinical Research Practice (GCP). The role involves training and supervising research staff, ensuring regulatory compliance, maintaining accurate documentation, and managing data collection and storage. You will interact with co-workers, visitors, and other staff consistent with our values, ensuring the smooth operation of clinical trials.

Responsibilities

• Oversee the day-to-day activities of clinical trials in accordance with GCP.

• Train and supervise research staff on proper procedures for conducting clinical trials per GCP.

• Prepare and submit all materials to the Institutional Review Board (IRB) and other regulatory bodies as required by the protocol.

• Maintain accurate subject logs, track expenses, and submit appropriate documentation to the Grant Administrator on a monthly basis.

• Perform regular quality control assessments to ensure data collection and storage per GCP.

• Organize and maintain documentation of all patient data.

• Design electronic capture databases and manage all collected data.

• Provide clerical and technical support to ensure adherence to research protocols and the quality of information received.

Essential Skills

• Clinical research

• Chart review

• Pre-screening patients

• Cardiovascular research

• Good Clinical Practice (GCP)

• Patient recruitment

• Electronic Data Capture (EDC)

• Medical knowledge

Additional Skills & Qualifications

• Minimum High School Diploma or equivalent

• Bachelor's Degree preferred

• Master's Degree is a plus

• High School Diploma or equivalent with 6 years of clinical research experience and SOCRA Certification required OR Bachelor's degree with 2 years of clinical research experience

• Strong organizational and documentation skills

Work Environment

The work environment is a combination of an office and hospital/outpatient surgery setting. The role involves a very fast-paced and high-volume workload, dealing with both industry and investigator studies. The position is hybrid, requiring on-site presence about three days a week. We offer excellent health benefits, tuition reimbursement once permanent, and opportunities for growth and upward mobility. You will be working on high-profile studies with well-known sponsors, providing great exposure to cardiovascular and device research.

Pay and Benefits

The pay range for this position is $28.00 - $33.00

• Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Philadelphia,PA.

Application Deadline

This position will be accepting applications until Jan 17, 2025.

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 ~~~ (~~~) for other accommodation options.