What are the responsibilities and job description for the Clinical Research Coordinator position at Novant Health Careers?
Job Summary
This candidate will be working in General Research. Preference for RNs with experience working in a Neurology and/or Cardiology Department OR Clinical Research Coordinators with at least 2 years of experience working on Neuro and/or Cardiology Studies.
The Clinical Research Coordinator (CRC) is a professional working under the direction of their Novant Health leader in conjunction with study investigators. Clinical Research Coordinators facilitate and coordinate daily clinical trial activities and play a critical role in the conduct of the study.
Our Clinical Research Coordinators are dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, qualify and compliance. They demonstrate knowledge of complex clinical research concepts gained through education and experience and work with a high degree of independence, using discretion and independent judgement in the executions of tasks. Human relations and interpersonal skills are necessary for interacting with patients and team members. Attention to detail and accuracy is necessary as is scheduling flexibility to accommodate protocol-required activity.
Our Clinical Research Coordinators possess excellent verbal and written communication skills, including telephone diplomacy. They have a working knowledge of information systems and database management functions as well as analytical and time management skills. Clinical Research Coordinators are self-motivated and able to work independently and on a team. They are able to prioritize and possess problem-solving skills, with demonstrated competency in applying clinical knowledge to patient management. Clinical Research Coordinators must be able to meet multiple deadlines for concurrent projects and have the knowledge and assessment skills to provide age-appropriate care and protocol requirement. While most Clinical Research Coordinators operate from a central location, there may be a need to travel within the healthcare system footprint for research patient care at regional clinics, or for training. No overnight travel is typically required.
Positions are primarily on-site, Monday through Friday. Some positions may offer Hybrid work opportunities.
Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship. Come join a remarkable team where quality care meets quality service, in every dimension, every time.
#JoinTeamAubergine #NovantHealth. Let Novant Health be the destination for your professional growth.
At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities.
#clinicalresearch #clinicaltrials #research #researchnurse #CRC #researchcoordinator #novanthealth
Responsibilities
It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time.
Candidates who meet any qualification level outlined below are encouraged to apply!
Non-Nursing Levels
Clinical Research Coordinator I
Clinical Research Coordinator II
Clinical Research Coordinator III
Clinical Research Coordinator IV
Previous experience in a healthcare setting or clinical research (CRA, Regulatory, clinic, CRO, pharma/biotech/device company, or other related experience).
Minimum 5 years* of clinical research experience required.
Minimum 10 years* of clinical research experience required. Certification in Clinical Research required.**
Minimum 15 years* of clinical research experience required. Certification in Clinical Research required.**
Nursing Levels: Must have current or compact RN licensure in the state of North Carolina. BSN/MSN preferred.
Clinical Research Coordinator I RN
Clinical Research Coordinator II RN
Clinical Research Coordinator III RN
Clinical Research Coordinator IV RN
Minimum 1 year* of nursing or clinical research experience required (CRA, Regulatory, clinic, floor, CRO, pharma/biotech/device company, or other related).
Minimum 5 years* of clinical research experience required.
Minimum 10 years* of clinical research experience required. Certification in Clinical Research required.**
Minimum 15 years* of clinical research experience required. Certification in Clinical Research required.**
55298
This candidate will be working in General Research. Preference for RNs with experience working in a Neurology and/or Cardiology Department OR Clinical Research Coordinators with at least 2 years of experience working on Neuro and/or Cardiology Studies.
The Clinical Research Coordinator (CRC) is a professional working under the direction of their Novant Health leader in conjunction with study investigators. Clinical Research Coordinators facilitate and coordinate daily clinical trial activities and play a critical role in the conduct of the study.
Our Clinical Research Coordinators are dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, qualify and compliance. They demonstrate knowledge of complex clinical research concepts gained through education and experience and work with a high degree of independence, using discretion and independent judgement in the executions of tasks. Human relations and interpersonal skills are necessary for interacting with patients and team members. Attention to detail and accuracy is necessary as is scheduling flexibility to accommodate protocol-required activity.
Our Clinical Research Coordinators possess excellent verbal and written communication skills, including telephone diplomacy. They have a working knowledge of information systems and database management functions as well as analytical and time management skills. Clinical Research Coordinators are self-motivated and able to work independently and on a team. They are able to prioritize and possess problem-solving skills, with demonstrated competency in applying clinical knowledge to patient management. Clinical Research Coordinators must be able to meet multiple deadlines for concurrent projects and have the knowledge and assessment skills to provide age-appropriate care and protocol requirement. While most Clinical Research Coordinators operate from a central location, there may be a need to travel within the healthcare system footprint for research patient care at regional clinics, or for training. No overnight travel is typically required.
Positions are primarily on-site, Monday through Friday. Some positions may offer Hybrid work opportunities.
Dedicated to excellence in all aspects of clinical research with a keen focus on ethics, safety, quality, compliance and stewardship. Come join a remarkable team where quality care meets quality service, in every dimension, every time.
#JoinTeamAubergine #NovantHealth. Let Novant Health be the destination for your professional growth.
At Novant Health, one of our core values is diversity and inclusion. By engaging the strengths and talents of each team member, we ensure a strong organization capable of providing remarkable healthcare to our patients, families and communities. Therefore, we invite applicants from all group dynamics to apply to our exciting career opportunities.
#clinicalresearch #clinicaltrials #research #researchnurse #CRC #researchcoordinator #novanthealth
Responsibilities
It is the responsibility of every Novant Health team member to deliver the most remarkable patient experience in every dimension, every time.
- Our team members are part of an environment that fosters team work, team member engagement and community involvement.
- The successful team member has a commitment to leveraging diversity and inclusion in support of quality care.
- All Novant Health team members are responsible for fostering a safe patient environment driven by the principles of "First Do No Harm".
Candidates who meet any qualification level outlined below are encouraged to apply!
Non-Nursing Levels
Clinical Research Coordinator I
Clinical Research Coordinator II
Clinical Research Coordinator III
Clinical Research Coordinator IV
Previous experience in a healthcare setting or clinical research (CRA, Regulatory, clinic, CRO, pharma/biotech/device company, or other related experience).
Minimum 5 years* of clinical research experience required.
Minimum 10 years* of clinical research experience required. Certification in Clinical Research required.**
Minimum 15 years* of clinical research experience required. Certification in Clinical Research required.**
Nursing Levels: Must have current or compact RN licensure in the state of North Carolina. BSN/MSN preferred.
Clinical Research Coordinator I RN
Clinical Research Coordinator II RN
Clinical Research Coordinator III RN
Clinical Research Coordinator IV RN
Minimum 1 year* of nursing or clinical research experience required (CRA, Regulatory, clinic, floor, CRO, pharma/biotech/device company, or other related).
Minimum 5 years* of clinical research experience required.
Minimum 10 years* of clinical research experience required. Certification in Clinical Research required.**
Minimum 15 years* of clinical research experience required. Certification in Clinical Research required.**
- Education may count toward years of experience.
- Accepted certifications in Clinical Research include the Association of Clinical Research Professionals (ACRP), the Society of Clinical Research Associates (SOCRA), Regulatory Affairs Professionals Society (RAPS) or Public Responsibility in Medicine and Research (PRIM&R).
- Additional Skills (required):
- Requires demonstrated knowledge of complex financial research concepts gained through education and experience. Works with a high degree of independence, using direction and independent judgement in the execution of tasks.
- Human relations and interpersonal skills necessary for interacting patients and team members.
- Attention to detail and accuracy necessary. Ability and willingness to work irregular hours as necessitated by research protocols. Excellent verbal and written communication skills. Excellent telephone diplomacy. Working knowledge of Information Systems and database management. Excellent analytical and time management skills. Self-motivated and able to work independently as well as a team. Ability to prioritize and problem-solving skills, with demonstrated competency in applying clinical knowledge to patient management. Able to meet multiple deadlines for concurrent projects. Knowledge and assessment skills to provide age appropriate care and protocol requirements.
- Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects Training, and International Air Transportation Association (IATA) certification for shipping hazardous and biological substances.
55298
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