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clinical research coordinator

Medical Center Ophthalmology Associates

<div>Company Overview:
<div>
Medical Center Ophthalmology Associates located in San Antonio Texas offers compassionate care for every eye condition. (MCOA) Board certified physician's offer comprehensive eyecare their team is totally dedicated to help you see better.</div>
Position Summary:
<div>
Medical Center Ophthalmology Associates (MCOA), in San Antonio, TX, is now hiring an enthusiastic Clinical Research Coordinator to join our growing team. The Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator, and the Research Director. The team member will implement and coordinate research and administrative procedures for the successful management of clinical trials.
</div>Responsibilities:
<div>
A CRC is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols.</div> 
<div></div><ul><li>
Administratively and clinically manage 5-7 concurrently running clinical research trials, including data collection, data query response, and issue resolution within a timely manner.</li><li>
Identify adverse events and report per protocol guidelines.</li><li>
Assist in the planning and design of source documents for study protocols.</li><li>
Conduct pre-study, initiation, monitoring, and close-out visits with sponsor representatives.
</li><li>Provide patient care, not limited to but including greeting patients in a friendly and prompt manner, responding within appropriate time frame to patient questions and communications, escorting patients to exam rooms, verifying patient information, making necessary documentation within patient charts, discussing study protocols with patients, and ensuring correct informed consent is documented.
</li><li>Work closely with physicians and doctors to update on changes in patient&rsquo;s health.
</li><li>Administer topical ophthalmic or oral medications.</li><li>
Maintain knowledge of operation and maintenance of clinical equipment, drugs, and supplies.
</li><li>Discuss study protocols with patients and verify the informed consent documentation</li><li>
Dispense study medication in a professional and accountable manner following protocol requirements</li><li>
Collect, process, and ship blood/urine specimens at scheduled patient visits</li><li>
Schedule all patient research visits and procedures consistent with protocol requirements</li><li>
Complete and maintain case report forms per FDA guidelines, and review them against the patient&rsquo;s medical record for completeness and accuracy</li><li>
Administer questionnaires/diaries per protocol.</li><li>
Maintain HIPAA compliance for all patient information.</li><li>
Adhere to all OSHA and Infectious Waste procedures.</li><li>
Obtain reading center certification and perform ophthalmic imaging and special testing when applicable</li><li>
Other duties as assigned.</li></ul>
Qualifications:
<div>
Education and/or Work Experience Requirements:</div><div><ul><li> 
2+ years in healthcare, preferably ophthalmology, but not necessarily in clinical research</li><li>Analytical mindset</li><li>Attention to detail</li><li>Exceptional interpersonal skills</li><li>Superior verbal and written communication skills</li><li>Understanding of laboratory procedures and equipment</li><li>Proficiency in MS Office &ndash; Word, Excel and Outlook</li><li>High school diploma or equivalent GED</li></ul></div><ul><li>Bilingual English/Spanish preferred.</li></ul> 
<div></div>
Company Benefits:

We offer a competitive benefits package to our employees:<ul><li>
Medical</li><li>
Dental</li><li>
Vision</li><li>
401k w/ Match</li><li>
HSA/FSA</li><li>
Telemedicine</li><li>
Generous PTO Package</li></ul>
We also offer the following benefits for FREE:<ul><li>
Employee Discounts and Perks</li><li>
Employee Assistance Program</li><li>
Group Life/AD&amp;D
</li><li>Short Term Disability Insurance
</li><li>Long Term Disability Insurance
</li></ul>EyeSouth Partners is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
#IND</div>

Clinical Research Coordinator

Doctors Hospital of Augusta

<div><h5 class="jobSectionHeader">Introduction</h5>
Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity. We care like family! Jump-start your career as a Clinical Research Coordinator today with Doctors Hospital of Augusta.<h5 class="jobSectionHeader">
Benefits</h5>
Doctors Hospital of Augusta offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:<ul><li>
Comprehensive medical coverage that covers many common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed medical transportation.</li><li>
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.</li><li>
Free counseling services and resources for emotional, physical and financial wellbeing 
</li><li>
401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service) 
</li><li>
Employee Stock Purchase Plan with 10% off HCA Healthcare stock 
</li><li>
Family support through fertility and family building benefits with Progyny and adoption assistance. 
</li><li>
Referral services for child, elder and pet care, home and auto repair, event planning and more 
</li><li>
Consumer discounts through Abenity and Consumer Discounts 
</li><li>
Retirement readiness, rollover assistance services and preferred banking partnerships 
</li><li>
Education assistance (tuition, student loan, certification support, dependent scholarships) 
</li><li>
Colleague recognition program 
</li><li>
Time Away From Work Program (paid time off, paid family leave, long- and short-term disability coverage and leaves of absence) 
</li><li>
Employee Health Assistance Fund that offers free employee-only coverage to full-time and part-time colleagues based on income.</li></ul> 
Learn more about Employee Benefits
Note: Eligibility for benefits may vary by location. 
Come join our team as a Clinical Research Coordinator. We care for our community! Just last year, HCA Healthcare and our colleagues donated $13.8 million dollars to charitable organizations. Apply Today!<h5 class="jobSectionHeader">
Job Summary and Qualifications</h5>
The Clinical Research Coordinator position is responsible for coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research.
Duties include but are not limited to:
<ul><li>Practice and adhere to the &ldquo;Code of Conduct&rdquo; philosophy and &ldquo;Mission and Value Statement&rdquo;
</li><li>During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.
</li><li>Performs routine operational activities for multiple research protocols
</li><li>Liaise between site research personnel, industry sponsors, and Supervisor
</li><li>Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable
</li><li>Coordinates schedule of assessments from initial submission of feasibility until study closeout
</li><li>Reviews the study design and inclusion/exclusion criteria with physician and patient
</li><li>Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
</li><li>Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
</li><li>Creates study specific tools for source documentation when not provided by sponsor
</li><li>Collects, completes, and enters data into study specific case report forms or electronic data capture systems
</li></ul>&middot; Generates and tracks drug shipments, device shipments, and supplies as needed &middot; Ensures timely and accurate data completion
<ul><li>Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
</li><li>Communicates all protocol-related issues to appropriate study personnel or manager
</li><li>Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required
</li><li>Reviews and responds to any monitoring and auditing findings
</li></ul>Education/Experience:
<ul><li>Bachelor&rsquo;s Degree required
</li><li>1+ years of relevant experience required
</li></ul>Certifications:
<ul><li>Certified Clinical Research Coordinator preferred
</li></ul>&quot;The great hospitals will always put the patient and the patient's family first, and the really great institutions will provide care with warmth, compassion, and dignity for the individual.&quot;- Dr. Thomas Frist, Sr. 
HCA Healthcare Co-Founder
If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Clinical Research Coordinator opening. We promptly review all applications. Highly qualified candidates will be contacted for interviews. Unlock the possibilities and apply today!
We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.</div>

Optima Dermatology

<div>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:
<ul>
<li>Maintain the highest level of professional conduct in the presence of investigators, subjects, research staff, sponsors, etc.</li>
<li>Able to perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study specific protocols</li>
<li>Computer skills with capability of using clinical trial databases, electronic data capture, Microsoft Word Office</li>
<li>Ability to communicate clearly using excellent verbal and written communications skills</li>
<li>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.</li>
<li>Ability to problem-solve, prioritize quickly and accurately and multi-task to facilitate work flow</li>
<li>Utilize negotiation skills to achieve expected results.</li>
<li>Ability to work independently in a fast-paced environment, as well as, work collaboratively as a team</li>
<li>Possess and utilize excellent interpersonal skills with patients, staff, and others</li>
<li>Meticulous and detail oriented</li>
<li>Ability to perform ECG, Phlebotomy, Urinary Pregnancy Test</li>
<li>Ensure proper collection, processing and shipment of bio specimens (e.g., centrifuge, freezing, refrigeration.</li>
</ul>
DUTIES AND RESPONSIBILITIES:
Regulatory:
<ul>
<li>Maintains a copy of all required Regulatory Documents for assigned portfolio of studies</li>
<li>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.</li>
<li>Maintains Master File with copies of all IRB communications for assigned portfolio of studies</li>
<li>Supports the safety of clinical research participants</li>
<li>Adhere to Good Clinical Practices and the study protocols</li>
<li>Any other duty which may be assigned to ensure all regulatory documentation occurs in a timely and thorough manner.</li>
</ul>
Clinical Trial Process:
<ul>
<li>Assists in facilitating and coordinating the daily clinical trial activities</li>
<li>Understands the details of each assigned portfolio of studies</li>
<li>Reviews and comprehends each protocol of assigned portfolio of studies including study proceedings and timeliness, inclusion and exclusion criteria, confidentiality and privacy protections</li>
<li>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</li>
<li>Assists in screening, recruiting and enrolling research participants</li>
<li>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</li>
<li>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.</li>
<li>Ensures the current approved Informed Consent is signed before Subjects are screened and enrolled in a clinical study</li>
<li>Provides research participants a copy of their signed Informed Consent.</li>
<li>Ensures participant's primary care physician receives notification of participant's participation in a study, if requested by the patient</li>
<li>Provides the receptionist with the target date and window for scheduling patient follow-up visits</li>
<li>Ensures adherence to protocol requirements</li>
<li>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</li>
<li>Dispense Investigational Article in a professional and accountable manner following protocol requirements</li>
<li>Maintains Investigational Article Dispensing Log</li>
<li>Continually reviews concomitant medications</li>
<li>Ensures appropriate specimen collection, processing and shipment per study protocol</li>
<li>Communicates abnormal laboratory values to appropriate persons in a timely manner.</li>
<li>Communicates regularly with Investigators about study progress and issues</li>
<li>Records all Adverse Events (AEs) reported by study participants</li>
<li>Reports all SAEs to Investigator, Sponsor's Clinical Research Associates (CRA), primary care physician and IRB</li>
<li>Administers questionnaires/diaries per protocol</li>
</ul>
Data Entry
<ul>
<li>Helps ensure that all required documentation are complete and appropriately filed for Sponsor Audits and/or FDA Inspections</li>
<li>Ensures all trial documentation (regulatory, IRB Communications, Subject and Investigational Article logs, etc.) are properly filed at trial closeout.</li>
<li>Accurately completes and maintains Case Review Forms (CRFs) (paper or electronic) per FDA guidelines and ensures all forms have been forwarded to the Sponsor</li>
<li>Maintains study source documents in the subject binder (e.g., medical history, laboratory reports, ECG, etc.)</li>
<li>Documents written and verbal communication with study contacts (e.g., research participant, sponsor, laboratory, etc.)</li>
<li>Completes and submits case report forms on as close to a &quot;real time basis&quot; as possible, but no greater than 48 hours after patient visit</li>
<li>Ensures that all study tasks information is completed so that invoices for study payments can be made in a timely and complete fashion</li>
<li>Store all files in a permanent, dry and safe location</li>
<li>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</li>
<li>Maintain a cooperative, helpful and pleasant affect, creating and/or contributing to an atmosphere of collaboration and team cohesiveness</li>
</ul>
Other:
<ul>
<li>Assists Data Entry Specialists in addressing queries and clarifications, as needed</li>
<li>Works with study monitors at site visits to resolve any outstanding issues or queries before the end of the site visit</li>
<li>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.
</li><li>Completes Continuing Education/In-service Education Requirements in the designated timeframe</li>
<li>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</li>
<li>Adheres to ICTC Policies and Procedures, Employee Guidebook and Standard Operating Procedures</li>
<li>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.</li>
<li>Performs additional duties as assigned by the Director of Clinical Research and/or Director of Site Operations to ensure the continuing success of ICTC</li>
<li>Assists other staff as needed or directed</li>
<li>Assists in the day-to-day operations, as needed and as assigned</li>
<li>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.</li></ul></div>

RadNet

<div>Job Description:

Artificial Intelligence; Advanced Technology; The very best in patient care. With decades of expertise, we are Radiology Forward. With dynamic cross-training and advancement opportunities in a team-focused environment, the core of our success is its people with the commitment to a better healthcare experience. When you join us as a Clinical Research Coordinator, you will be joining a dedicated team of professionals who deliver quality, value, and access in the 21st century and align all stakeholders- patients, providers, payors, and regulators to achieve the best clinical outcomes. 
You Will:<ul><li>
Works with broad spectrum of health care providers for many disease types, physicians, nurses, other research coordinators, imaging techs and support staff</li><li>
Read and interpret research study protocols in order to define the procedures that will be provided to the clinical research site</li><li>
Translate the designated study procedures into a plan for operational implementation</li><li>
Must be able to articulate study process and produce study flow and source documents that are instructive to the technical and clerical staff</li><li>
Maintain impeccable records of all interactions with clients and companies</li><li>
Assures confidentiality of patient&rsquo;s records and study related materials that are provided under non-disclosure agreements by the research site, pharmaceutical company, or imaging vendor</li><li>
Assist the scheduling team with any problems or difficulties to achieve patient study time lines</li><li>
Maintains accurate study files</li><li>
Provides each imaging site with binders and assists them with relevant information in order to procure correct imaging for each study</li><li>
Visits multiple imaging centers in California to ensure training and study compliance.</li><li>
Attends on site pre study and site initiation visits as needed</li><li>
Adjusts schedule to ensure site visits and training sessions can be accomplished</li><li>
Must be able to problem solve and resolve data queries in a timely manner</li><li>
Work environment is organized and functions efficiently</li></ul>
You Are:<ul><li>
Genuinely passionate about customer service and exercise sound judgement and an ability to remain professional in all situations</li><li>
Able to demonstrate high level of attention to detail, excellent organizational skills and have the ability to multitask</li><li>
Able to thrive in a fast-paced environment, have a knack for prioritizing work with a structured approach, and enjoy providing world class customer service</li></ul>
To Ensure Success In This Role, You Must Have:<ul><li>
High school graduate (some college preferred)</li><li>
MA certificate, or at least 2 years in a clinical setting or imaging center</li><li>
At least 2 years in a research environment with study operations responsibilities</li><li>
Bachelor&rsquo;s degree or higher may substitute for experience</li></ul>
We Offer:
<ul><li>Comprehensive Medical, Dental and Vision coverages.</li><li>
Health Savings Accounts with employer funding.</li><li>
Wellness dollars</li><li>
401(k) Employer Match</li><li>
Free services at any of our imaging centers for you and your immediate family.</li></ul>
Pay Range: USD $21.00 - USD $23.00 /per hour Shift: Mornings Shift Variations: Monday-Friday ;8:00 am &ndash; 4:30 pm shift, 30 mins lunch</div>

DelRicht Research

<div>Why DelRicht Research?

Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer is yes, then DelRicht Research might be the right opportunity for you! 

Who We Are

DelRicht is a clinical research company dedicated to providing an excellent customer experience to all patients that participate in our clinical trials. Our clinical trials provide new treatment options for our patients and ultimately our goal is to get new medications and medical devices FDA approved! We hold our team members to a high standard of excellence and are looking for energetic, positive, quick learners to be a part of our team. Presently our network stretches across 33 sites throughout the United States in 18 states. 

DelRicht Research has been recognized as a Top Workplace for 2023, 2024, and 2025! This is a testament to our unwavering commitment to creating an exceptional work environment that fosters growth, collaboration, and employee satisfaction. 

Clinical Research Coordinator&rsquo;s Main Objective: Overall, the Clinical Research Coordinator is responsible for providing quality, excellent patient care and a great experience for our patients in our clinical research studies:
<ul>
<li>Patients have a fun, positive and comfortable experience at our clinic</li>
<li>Patient visits are completed accurately and efficiently seeing to it that all clinical trial protocols are being adhered to 100% of the time</li>
<li>Patient recruitment and enrollment into clinical trials</li>
<li>Ensuring patients come to and complete their clinical trial visits throughout the study</li>
<li>Data Entry timely and accurately entered for clinical visits into multiple online systems</li>
<li>Lead and main point of contact for Pharmaceutical Sponsors and Contract Research Organizations for all clinical trials</li>
<li>Ensuring Sponsors and Clients have amazing customer service when they are onsite at our clinic and assuring we are always providing clear, constant communication with them when they are off site</li>
<li>Maintaining Physician Trust - You are seen as a go to, knowledgeable resource to our physicians including ensuring the physician is well informed of their schedule and updated on all current clinical trial patients and protocols</li></ul> 
 
Skills needed to win: 
<ul>
<li>Preferred: Minimum of 1 year of experience in any patient facing or customer service position 
</li>
<li>Preferred: 2+ years of professional work experience 
</li>
<li>Preferred: B.S or B.A from any accredited university, or 2+ years of professional work experience in a healthcare or clinical setting</li>
<li>This is an onsite Monday-Friday position. 
</li>
<li>Coffee drinkers preferred. Tea drinkers accepted.</li></ul> 
 
The Right Candidate Will:
<ul>
<li>Be self motivated! Energetic! Positive!</li>
</ul><ul><li>Focus on providing exceptional patient care and creating memorable experiences</li>
</ul><ul><li>Make sure client satisfaction is a primary focus and that the client is able to achieve and exceed their goals</li>
</ul><ul><li>Believe in high quality and have a high standard of compliance to our study protocols</li>
</ul><ul><li>Be remarkably organized</li>
</ul><ul><li>Be skilled at problem solving, planning and being proactive</li>
<li>Accept ownership of tasks from inception through completion and assume responsibility for personal success</li></ul> 
 
DelRicht Research&rsquo;s Core Values: Production, Humility, Consistency

Production:
<ul>
<li>We deliver on our promises</li>
<li>We have a bias towards action: we value independent problem solving</li>
<li>We proactively over deliver: we can act without being told what to do and we always have new ideas that will be heard and will improve the company</li> 
</ul>
Humility:
<ul>
<li>We support each other relentlessly</li>
<li>We always have enthusiasm: we exhibit passion and excitement about our work which leads to everyone having a &lsquo;can do&rsquo; attitude</li>
<li>We embrace change: we are excited to always be growing and moving the organization forward which means change is the norm for us</li>
<li>Coachable: we all love to learn, we are willing to be taught and will adapt quickly</li> 
</ul>
Consistency:
<ul>
<li>We always are able to execute: we get it right the first time and promote &lsquo;touch it once&rsquo; accuracy</li>
<li>We have persistence: we demonstrate the tenacity and willingness to go the distance to get something done</li>
<li>We are calm under pressure: we can maintain stable performance when under heavy pressure or stress</li></ul> 


Team Perks &amp; Benefits at DelRicht Research:
<ul>
<li>Medical Insurance, with generous employer paid contributions</li>
<li>Dental and Vision Insurance</li>
<li>Short and Long Term Disability and Group Life Coverage</li>
<li>Paid Time Off that builds throughout your career with the company</li>
<li>401K (+ discretionary match/profit sharing)</li>
<li>Quarterly Bonus Plan that clearly outlines your bonus potential per quarter and giving the team the visibility and control to maximize earnings by hitting team goals</li>
<li>Professional Development Program tailored to each team member&rsquo;s profess goals. Our quarterly goal-setting initiative is designed to challenge our team members to reach and exceed their potential!</li>
<li>Success-Driven Environment where data drives our decisions and insights. Be a part of a winning team that prioritizes transparency, continuous improvement, and success!</li> 
</ul>
Job Type: Full-Time 40+ hrs 
Visit our website linked below to learn about our company and current clinical trials, see patient testimonials, and check out our careers page!

Website: www.delrichtresearch.com

Patient Testimonials: https://delrichtresearch.com/testimonials/ 

We are an equal opportunity employer and consider all qualified applicants equally without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.</div>

OhioHealth

<div>We are more than a health system. We are a belief system. We believe wellness and sickness are both part of a lifelong partnership, and that everyone could use an expert guide. We work hard, care deeply and reach further to help people uncover their own power to be healthy. We inspire hope. We learn, grow, and achieve more &ndash; in our careers and in our communities.
Job Description Summary:
The Clinical Consultant Research works in collaboration with the Principal Investigator (PI) to coordinate assigned clinical research studies in accordance with Good Clinical Practice (GCP) guidelines and federal regulations. This position performs basic day to day activities related to clinical research studies including: recruit and screen participants, obtains informed consent, educate participants regarding study requirements, event reporting, collection of and organizes research data and complete case report forms. This position applies basic level of understanding to the ability to perform a variety of tasks under direct supervision in a range of different type of clinical studies.
Responsibilities And Duties:
Study Planning and Coordination
 
Assists with implementation and coordination of research studies and projects.
 
Accountable to PI for study specific responsibilities.
 
Works closely with PI and direct supervisor to organize, plan and carry out the research in an efficient and timely manner.
 
Assists with protocol feasibility, resource requirements and study planning activities including leading internal training to implement the protocol and avoid deviations.
 
Assists with recruitment procedures for potential participants and oversees the enrollment of the clinical trial as directed by the PI.
 
Ensures that study parameters are correctly applied prior to a research participant enrolling in a study and during the research participant&rsquo;s visits and assessments.
 
Extracts and records physical findings, laboratory data and other details essential to each study onto the required data collection forms accurately and within the designated time
 
Attends investigator&rsquo;s meetings, pre-study site visits which may require travel, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.
 
Participates in in-house protocol meetings to review study-related procedures, staffing and visit flow.
 
Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant&rsquo;s responsibilities in the study.
 
Responsible for giving participant instructions and serves as the primary contact for subjects by being available to handle study specific questions, concerns or events.
 
Accurately records and extracts data from source documentation onto required data collection forms (paper or electronic) in a timely manner. Maintains accurate and timely source documentation.
 
Prepares study documents for archiving according to timelines, following closeout visits activities
 
Responsible for in-depth knowledge of protocol requirements and GCP guidelines.
 
Performs other related duties as assigned or required.
 
 
Patient Care
 
Assists nursing and clinical staff and applies skills and knowledge to facilitate the care of research participants.
 
Assists nursing and clinical staff and utilizes knowledge of disease processes to observe, report adverse events, and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.
 
 
Quality and Compliance
 
Assists in audit preparedness activities for OHRI.
 
Assists with monitoring visits on site or remotely and is available during visits for corrections, questions, etc.
 
Maintains study records according to sponsor and/or regulations.
 
Keep records in a secure location.
 
 
Reporting
 
Assist in the development of reporting metrics.
 
Generates reports and reviews to ensure validity of data.
 
Provide ad hoc reports.
 
 
Communication
 
Demonstrates effective communications skills.
 
Communicates information in a timely and accurate manner.
 
Functions as a liaison with sponsor and investigator regarding the preparation, execution and completion of studies.
 
Adapts communication skills in response to various situations including those related to differences in culture, age, education and other communication barriers.
 
Uses various media forms to maximize communication success.
 
Demonstrates teamwork characteristics.
 
Ability to manage time, prioritize and follow up on projects as necessary taking into consideration the need for flexibility when working on multiple projects.
 
Participates in meetings with OHRI, PI and clinical teams to review patient status at a detailed level.
 
Works with research staff to effectively communicate patient process for each trial for the life of the study.
 
Advise, communicate and reinforce standard practices, regulations to following regarding research study participation.
 
 
Other
 
Attends relevant training courses on policy and compliance.
 
Ensures assigned training is complete and meets internal qualifications.
 
Responsible for completing all necessary training for their position.
 
Maintain familiarity with evolving regulatory and compliance context.
 
Other duties as assigned.
Minimum Qualifications:
Bachelor's Degree (Required)
Additional Job Description:
required from a four year college or university
SPECIALIZED KNOWLEDGE
Ability to prioritize assigned work
Strong verbal and written communication skills, as well as customer service skills and ability to problem solve, prioritize and manage multiple tasks
Strong computer skills, including thorough knowledge of systems (EMR, Microsoft)
DESIRED ATTRIBUTES
One year of relevant work or academic experience preferred
Prior experience in a medical environment preferred
Clinical Research Coordinator Certification (or equivalent approved Clinical Research Certification)
One or more years of direct human subjects research
Clinical knowledge in assigned therapeutic area or program 
 
MAJOR DUTIES/RESPONSIBILITIES &amp; ESSENTIAL FUNCTIONS
Study Planning and Coordination
Assists with implementation and coordination of research studies and projects.
Accountable to PI for study specific responsibilities.
Works closely with PI and direct supervisor to organize, plan and carryout the research in an efficient and timely manner.
Assists with protocol feasibility, resource requirements and study panning activities including leading internal training to implement the protocol and avoid deviations.
Assist with recruitment procedures for potential participants and oversee the enrollment of the clinical trial as directed by the PI.
Ensures that study parameters are correctly applied prior to a research participant enrolling a study and during the research participant&rsquo;s visits and assessments.
Extracts and records physical findings, laboratory data and other details essential to each study onto the required data collection forms accurately and within the designated time period
Attends investigator&rsquo;s meetings, pre-study site visits which may require travel, study initiation visits, and all other study-related visits by monitors or Sponsor representatives.
Participate in in-house protocol meetings to review study-related procedures, staffing and visit flow.
Participates in the ongoing Informed Consent process with the Investigator to ensure that research participants and their families (if applicable) have their questions answered and understand the consent form, as well as participant&rsquo;s responsibilities in the study.
Responsible for giving participant instructions and serves as the primary contact for subjects by being available to handle study specific questions, concerns or events.
Accurately records and extracts data from source documentation onto report forms (paper or electronic) in a timely manner. Maintains accurate and timely source documentation.
After closeout visits have been conducted, prepares study documents for archiving according to timelines.
Responsible for in-depth knowledge of protocol requirements and GCP guidelines.
Performs other related duties as assigned or required.
Patient Care
Assists nursing and clinical staff and applies skills and knowledge to facilitate the care of research participants.
Assists nursing and clinical staff and utilizes knowledge of disease processes to observe and report adverse events and protocol violations / deviations in a timely and accurate manner to the Investigator to ensure the health, safety and welfare of the participant.
Quality and Compliance
Assists in audit preparedness activities for OHRI.
Assists with monitoring visits on site and is available during visits for corrections, questions, etc.
Maintains study records according to sponsor and/or regulations.
Keep records in a secure location.
Reporting
Assist in the development of reporting metrics.
Generates reports and reviews to ensure validity of data.
Provide ad hoc reports.
Communication
Demonstrates effective communications skills.
Communicates information in a timely and accurate manner.
Functions as a liaison with sponsor and investigator regarding the preparation, execution and completion of studies.
Adapts communication skills in response to various situations including those related to differences in culture, age, education and other communication barriers.
Uses various media forms to maximize communication success.
Demonstrates teamwork characteristics.
Ability to manage time, prioritize and follow up on projects as necessary taking into consideration the need for flexibility when working on multiple projects.
Participates in meetings with OHRI, PI and clinical teams to review patient status at a detailed level.
Work with research staff to effectively communicate patient process for each trial for the life of the study.
Advise, communicate and reinforce standard practices, regulations to following regarding research study participation.
Other
Attends relevant training courses on policy and compliance.
Ensures assigned training is complete and meets internal qualifications.
Responsible for completing all necessary training for their position.
Maintain familiarity with evolving regulatory and compliance context.
Other duties as assigned.
Work Shift:
Day
Scheduled Weekly Hours :
40
Department
Heart &amp; Vascular Research Clinical Services
Join us!
 
... if your passion is to work in a caring environment
 
... if you believe that learning is a life-long process
 
... if you strive for excellence and want to be among the best in the healthcare industry
Equal Employment Opportunity
OhioHealth is an equal opportunity employer and fully supports and maintains compliance with all state, federal, and local regulations. OhioHealth does not discriminate against associates or applicants because of race, color, genetic information, religion, sex, sexual orientation, gender identity or expression, age, ancestry, national origin, veteran status, military status, pregnancy, disability, marital status, familial status, or other characteristics protected by law. Equal employment is extended to all person in all aspects of the associate-employer relationship including recruitment, hiring, training, promotion, transfer, compensation, discipline, reduction in staff, termination, assignment of benefits, and any other term or condition of employment</div>

Beth Israel Lahey Health

Boston, MA &bull; Beth Israel Deaconess Medical Center &bull; Per Diem &bull; Day
 <div>When you join the growing BILH team, you're not just taking a job, you&rsquo;re making a difference in people&rsquo;s lives.

Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results. Works closely with other clinical research staff.

Job Description:

Primary Responsibilities:

1. Independently or in conjunction with other clinical research staff and/or research nurse, recruits and enrolls research subjects onto clinical research projects according to study protocols. May assess research subjects' eligibility for inclusion in a particular protocol based on contracts with physicians and nurses and knowledge of the protocol. (essential)

2. Checks all eligibility and ineligibility criteria with the research subjects' medical record. Verifies information with clinical research nurse and/or principal investigator. (essential)

3. Discusses informed consent with research subjects. Interacts with research subjects prior to entering the study and throughout the entire treatment. Assists with scheduling appointments and follow up tests. (essential)

4. Learns protocol and monitors strict adherence to protocols by physicians, nurses and research subjects. Reviews protocol requirements with physicians, nurses and fellows. Identifies any problems with protocol compliance and notifies principal investigator and/or research nurse. Begins to learn how to independently resolve problems with protocol. (essential)

5. Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols. Enters data into computerized system. (essential)

6. Assists clinic staff in obtaining insurance approval for subject protocol participation and scheduling tests and arranging admissions or outpatient visits for subjects. (essential)

7. Assists investigator with correspondence with IRB. (essential)

8. As needed, may function in areas/clinics performing job duties related to clinical research studies.

Required Qualifications:
<ul>
<li>Bachelor's degree required.
</li>
<li>0-1 year of related work experience required.
</li>
<li>Medical terminology.
</li>
<li>Working knowledge of computer systems required, including web-based applications and some Microsoft Office applications, which may include Outlook, Word, Excel, PowerPoint or Access.
</li>
</ul>Competencies:

Decision Making: Ability to make decisions that are based on specific instructions, standard practices and established procedures which generally require little or no supervision.

Problem Solving: Ability to address problems that are routine, somewhat repetitive and generally solved by following clear directions and procedures and by identifying opportunities for process improvements.

Independence of Action: Ability to follow general instructions and procedures as provided. Work is monitored by supervisor/manager.

Written Communications: Ability to communicate clearly and effectively in written English with internal and external customers.

Oral Communications: Ability to comprehend and converse in English to communicate effectively with medical center staff, patients, families and external customers.

Knowledge: Ability to demonstrate full working knowledge of standard concepts, practices, procedures and policies with the ability to use them in varied situations.

Teamwork: Ability to work collaboratively in small teams to improve the operations of immediate work group by offering ideas, identifying issues, and respecting team members.

Customer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving. Ability to remain calm in stressful situations.

Physical Requirements: 
Light work: Exerting up to 20 pounds of force frequently to move objects. Some elements of the job are sedentary, but the employee will be required to stand for periods of time or move throughout the hospital campus. 


Pay Range:
$19.23 &ndash; $28.37

The pay range listed for this position is the base hourly wage range the organization reasonably and in good faith expects to pay for this position at this time. Actual compensation is determined based on several factors, that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other applicable factors permissible by law. Compensation may exceed the base hourly rate depending on shift differentials, call pay, premium pay, overtime pay, and other additional pay practices, as applicable to the position and in accordance with the law.

<h2 class="jobSectionHeader">As a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment.</h2>

<h2 class="jobSectionHeader">More than 35,000 people working together. Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives. Your skill and compassion can make us even stronger.</h2>

<h2 class="jobSectionHeader">Equal Opportunity Employer/Veterans/Disabled</h2></div>
 <div><h3 class="jobSectionHeader">Job details</h3>
<ul><li><div>Employment: Per Diem</div></li>
<li><div>Shift: Day</div></li>
<li><div>Category: Medical/Clinical Research</div></li>
<li><div>Pay Range: $19.23 - $28.37</div></li>
<li><div>FLSA: Non-Exempt</div></li>
<li><div>Req ID: JR88348</div></li></ul></div>

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