Clinical Research Coordinator at Optima Dermatology

Boardman, Ohio, United States -

Full Time

Start Date

Immediate

Expiry Date

29 Jan, 26

Salary

0.0

Posted On

01 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Regulatory Compliance, Informed Consent, Data Entry, Patient Recruitment, Adverse Event Reporting, Good Clinical Practices, Organizational Skills, Communication Skills, Problem-Solving, Interpersonal Skills, ECG, Phlebotomy, Specimen Collection, Time Management, Team Collaboration

Industry

Hospitals and Health Care

Description

POSITION SUMMARY The Clinical Research Coordinator (CRC) is responsible for a variety of activities in support of clinical research studies. The CRC works closely with and carries out the directives of the Director of Clinical Research in all aspects of the care and treatment of clinical research subjects in compliance with study protocols throughout the research study. The CRC is responsible for his/her assigned portfolio of studies as it relates to, but not limited to, the following areas: regulatory requirements; informed consent; recruitment; accurate and timely completion of case report forms, patient visits (paper and electronic); data entry; laboratory; test article; adverse event reporting; and study close out. The CRC is required to have knowledge of protocol design and Good Clinical Practices (GCP) as set forth by the Federal Regulations and International Conference of Harmonization (ICH) Guidelines for the protection of human subjects and the conduct of clinical research required Knowledge of the International Air Transport Association (IATA) regulations for the transportation of Dangerous Goods is also necessary. Under the direction of the Director of Site Operations, the CRC will help ensure protocol compliance, Investigational Article accountability and proper follow-up during the clinical trial. TYPICAL PHYSICAL DEMANDS: Physically capable of lifting, moving or transporting supplies, medical records and equipment within reasonable weight limits. Physically capable of reading and reviewing handwritten chart notations. Physically capable of bending, sitting or standing for extended periods of time, reaching and climbing to retrieve or store medical records. Physically capable of manually entering data into an electronic data base using a keyboard. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. TYPICAL WORK CONDITIONS: Fast-paced clinical research center environment. Must be able to adjust and adapt to changing conditions. QUALIFICATIONS, REQUIREMENTS and EDUCATION: Minimum: High School Diploma with two years clinical research coordinator experience. Preferred: Associates Degree in a medical related field and one-year clinical research experience. Candidate will be required to sit for and successfully obtain CCRC after two years clinical research coordinator experience. Travel within the USA to attend Investigator meetings for new clinical trials may be required. ESSENTIAL SKILLS: Maintain the highest level of professional conduct in the presence of investigators, subjects, research staff, sponsors, etc. Able to perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols Computer skills with capability of using clinical trial databases, electronic data capture, Microsoft Word Office Ability to communicate clearly using excellent verbal and written communications skills Possess exceptional organizational and prioritization skills as demonstrated by planning objectives and strategies to ensure that the process/requirements for the flow of clinical research information is optimized; such as: charting is completed accurately and thoroughly and subject binder provided to Data Entry for EDC processing within 48 hours of the patient visit. Ability to problem-solve, prioritize quickly and accurately and multi-task to facilitate work flow Utilize negotiation skills to achieve expected results. Ability to work independently in a fast-paced environment, as well as, work collaboratively as a team Possess and utilize excellent interpersonal skills with patients, staff, and others Meticulous and detail oriented Ability to perform ECG, Phlebotomy, Urinary Pregnancy Test Ensure proper collection, processing and shipment of bio specimens (e.g., centrifuge, freezing, refrigeration. DUTIES AND RESPONSIBILITIES: Regulatory: Maintains a copy of all required Regulatory Documents for assigned portfolio of studies Assists DSO and/or DCR in preparing for IRB submissions, protocol revisions, periodic or final reports, and submitting timely and accurate regulatory documents to sponsors, as needed. Maintains Master File with copies of all IRB communications for assigned portfolio of studies Supports the safety of clinical research participants Adhere to Good Clinical Practices and the study protocols Any other duty which may be assigned to ensure all regulatory documentation occurs in a timely and thorough manner. Clinical Trial Process: Assists in facilitating and coordinating the daily clinical trial activities Understands the details of each assigned portfolio of studies Reviews and comprehends each protocol of assigned portfolio of studies including study proceedings and timeliness, inclusion and exclusion criteria, confidentiality and privacy protections Participates in the pre-screening of potential research participants to determine their initial eligibility and interest in a research study and adhering to important guidelines to protect the privacy of the patients Assists in screening, recruiting and enrolling research participants Participates in the Informed Consent process by communicating clearly and openly with potential study patients about; protocols open to enrollment, explains the purpose, duration, risk/benefits of the study and obtains all required signatures Possesses a thorough knowledge of the Informed Consent process, as well as, a thorough understanding of the study protocol (s) in order to answer all questions pertaining to the study posed during the Informed Consent process. Ensures the current approved Informed Consent is signed before Subjects are screened and enrolled in a clinical study Provides research participants a copy of their signed Informed Consent. Ensures participant’s primary care physician receives notification of participant’s participation in a study, if requested by the patient Provides the receptionist with the target date and window for scheduling patient follow-up visits Ensures adherence to protocol requirements Assists the Director of Clinical Research with requirements of patient visits per study protocol, such as: obtaining vital signs, documenting assessment of patient response to Investigational Article and evaluation of Adverse Events (AEs); retrieving Investigational Article and documenting Subject compliance with required dosage Dispense Investigational Article in a professional and accountable manner following protocol requirements Maintains Investigational Article Dispensing Log Continually reviews concomitant medications Ensures appropriate specimen collection, processing and shipment per study protocol Communicates abnormal laboratory values to appropriate persons in a timely manner. Communicates regularly with Investigators about study progress and issues Records all Adverse Events (AEs) reported by study participants Reports all SAEs to Investigator, Sponsor’s Clinical Research Associates (CRA), primary care physician and IRB Administers questionnaires/diaries per protocol Data Entry Helps ensure that all required documentation are complete and appropriately filed for Sponsor Audits and/or FDA Inspections Ensures all trial documentation (regulatory, IRB Communications, Subject and Investigational Article logs, etc.) are properly filed at trial closeout. Accurately completes and maintains Case Review Forms (CRFs) (paper or electronic) per FDA guidelines and ensures all forms have been forwarded to the Sponsor Maintains study source documents in the subject binder (e.g., medical history, laboratory reports, ECG, etc.) Documents written and verbal communication with study contacts (e.g., research participant, sponsor, laboratory, etc.) Completes and submits case report forms on as close to a “real time basis” as possible, but no greater than 48 hours after patient visit Ensures that all study tasks information is completed so that invoices for study payments can be made in a timely and complete fashion Store all files in a permanent, dry and safe location Prepare for clinical trial monitor site visits; assist and provide requested information during the visit to facilitate a pleasant and optimal experience for the monitor Maintain a cooperative, helpful and pleasant affect, creating and/or contributing to an atmosphere of collaboration and team cohesiveness Other: Assists Data Entry Specialists in addressing queries and clarifications, as needed Works with study monitors at site visits to resolve any outstanding issues or queries before the end of the site visit For assigned portfolio of studies, works toward resolving all unresolved flagged issues within one week of the site visit and reports completion status or progress toward resolution to the Director of Site Operations. It is expected that all outstanding issues will be resolved prior to the next monitor visit. Completes Continuing Education/In-service Education Requirements in the designated timeframe Maintains current training in the following areas: OSHA training regarding Bloodborne Pathogens; International Air and Transportation Association (IATA) training for routine packaging, labeling and transporting of biological materials; Basic Life Support (BLS) and AED training Adheres to ICTC Policies and Procedures, Employee Guidebook and Standard Operating Procedures Consistently demonstrates support for compliance in the performance of job duties and responsibilities by developing and maintaining knowledge of and performing job functions in compliance with rules, regulations, policies and statutes that affect the CRC job function. Performs additional duties as assigned by the Director of Clinical Research and/or Director of Site Operations to ensure the continuing success of ICTC Assists other staff as needed or directed Assists in the day-to-day operations, as needed and as assigned Provide the Director of Site Operations with a report of CRC activities, outstanding issues, assignment progress and/or completion, prep for upcoming monitoring visits, etc.

Responsibilities

The Clinical Research Coordinator (CRC) is responsible for managing clinical research studies, ensuring compliance with protocols, and maintaining regulatory documentation. The CRC also facilitates patient recruitment, informed consent processes, and data entry for clinical trials.