What are the responsibilities and job description for the Clinical Research Coordinator position at Actalent?
Description:
We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position of Clinical Research Coordinator (CRC). This role is responsible for the successful conduct of clinical trials under the oversight of the principal investigator. The CRC will be responsible for both clinical and administrative duties related to the conduct of clinical research at the site.
Clinical Research Nurse Coordinator Responsibilities:
Abide by local, state, GCP, ICH and FDA guidelines and regulations for the conduct of clinical trials.
Overseeing the smooth running of clinical trials at site in collaboration with study investigator(s).
Complete all required organization and study specific training in timely manner, including attendance at offsite investigator meetings
Supervision and training of site research site staff, including study coordinators, research assistants and tab technicians
Participate in the planning and conduct of research participant recruitment efforts
Conduct the proper consenting of research participants
Collecting source obtained from research and transcribe into case report forms.
Perform medically qualified clinical procedures such as vital signs, EKG and phlebotomy
Process study labs per requirements
Provide clinical research training and mentoring to study team.
Provide responsive and diligent collaboration with sponsor/CRO study teams, including prompt resolution of queries and other action items.
Monitoring research participants to ensure adherence to study participation.
Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
Engaging with subjects and understanding their concerns.
Clinical Research Coordinator Requirements:
3 years’ experience as a clinical research coordinator on phase II & III studies
Currently trained or willing to be trained in phlebotomy, performance of vital signs, medical history collection, and administration of EKGs
Attention to detail
Exceptional interpersonal and customer service skills
Outstanding written and verbal communication
Excellent organizational skill
Willingness to continually self-educate
Additional:
Bilingual in Spanish/English
Skills:
phlebotomy, patient recruitment, informed consent, Clinical research, Clinical trial, Clinical research coordinator, Clinical site coordinator, bilingual
Top Skills Details:
phlebotomy,patient recruitment,informed consent
Additional Skills & Qualifications:
clinical research coordinator
high enrolling- up to 4 patients per day and documentation
Experience Level:
Intermediate Level
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
Actalent is an equal opportunity employer.
About Actalent
Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
Salary : $28 - $32
