Oncology Clinical Research Coordinator Jobs in Arkansas

Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or

High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection

UAMS offers amazing benefits and perks

Education discount for staff and dependents (undergraduate only)

Career Training and Educational Opportunities

May participate in the identification and response to potential and actual risk management issues.

5+ years experience in a hospital/medical environment and 1 year supervisory

Coordinates care delivery and the assignment of staff based upon identified patient care needs and clinical competency for optimal unit operations.

Collaborates with members of the health care team in program development, consultation, and the planning and delivery of optimal unit operations.

Facilitates timely and responsive communication and proactive responsible decision making.

May arrange for the availability of human and material resources to facilitate positive outcomes for assigned research projects.

Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.

Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.

Prepares and ensures grant applications, IRB/GCO documents are submitted.

Ensures accurate and complete compilation of subject data through chart reviews.

Independently obtains informed consent for other clinical studies.

Mentors Clinical Research Coordinators in training.

3+ years of industry-sponsored clinical trial management experience required.

Prior experience with clinical protocol development and/or regulatory submissions and management

Proactive stakeholder management and communication of progress and issues

Strong knowledge of clinical operations and the regulatory process - experience independently running/managing multiple clinical trials preferably within the oncology area

EDC including trial management, data review, issuing and resolving queries, CRF design/review/ approval

Additional post-graduate scientific experience or qualifications, such as an M.Sc. or PhD

Bachelors degree in science or related field preferred or a combination of relevant research experience and education

0-2 years of research/human subjects experience

Assists in the collection, analysis and review of experimental data for publication and presentation.

May secure and ship clinical specimens as required by the protocol.

May assist in the preparation for regulatory agency site visits.

Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.

Remote, onsite, and hybrid opportunities available

Clinical Research Coordinators II/III roles are consulting (contractor) roles. These are not permanent position with benefits.

The benefits of enjoying the Advarra team include:

•Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy

Potentially higher hourly pay rate than working direct

Bachelors degree in science or related field preferred or a combination of relevant research experience and education

0-2 years of research/human subjects experience

Assists in the collection, analysis and review of experimental data for publication and presentation.

May secure and ship clinical specimens as required by the protocol.

May assist in the preparation for regulatory agency site visits.

Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.

Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.

Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.

Prepares and ensures grant applications, IRB/GCO documents are submitted.

Ensures accurate and complete compilation of subject data through chart reviews.

Independently obtains informed consent for other clinical studies.

Mentors Clinical Research Coordinators in training.

Can demonstrate experience and knowledge in the CRO industry that will support POI’s management of clinical trials.

Assist the Project Team with the day-to-day management of clinical studies as required.

Monitoring Visit Report (MVR) review, management, resolution and escalation as required.

Relevant life science degree / medical / nursing background, or combination of education and experience.

Proven organizational abilities, and excellent written and oral communication and presentation skills.

A thorough knowledge of regulatory submission and reporting requirements and guidelines.

Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).

Strong knowledge of investigational protocols especially with pediatric protocols (data management, query resolution, protocol design, protocol writing and protocol implementation).

Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.

Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.

Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.

Experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.

M.D., or D.O. with subspecialty and board eligibility/certification in oncology

Significant experience in Oncology drug development may substitute for oncology specialization

Minimum of 3 years of successful clinical research and/or drug development experience in biologics

Possesses early phase clinical development experience

Clinical development experience in the pharmaceutical/biotechnology industry or academic medical setting

Interacts closely with the pre-clinical team to understand the scientific basis of targeted therapy and the relationship to clinical practice decision-making.