Clinical Research Nurse Resume Sample
Rose Stoltenberg
265 Sandrine Cliffs,
Boston,
MA
+1 (555) 622 9997
Work Experience
Clinical Research Nurse Manager
09/2016
-
PRESENT
Phoenix, AZ
- Performs conduct procedures in strict compliance to the study protocol, Good Clinical Practice standards, Standard Operating Procedures (SOP’s), QA/QC procedures, OSHA guidelines and other state and local regulations as applicable
- Acts as a liaison between study sponsors, study monitors, principal investigators, other physicians, hospital staff, and the Institutional Review Board (IRB) to coordinate the efforts necessary to efficiently and effectively conduct a clinical research study
- Actively participate in the selection of studies TriHealth conducts, developing a process for implementation of the protocol, participating in the identification of potential subjects, participating in the informed consent process, enrolling subjects and accurately and thoroughly collecting and reporting data
- Educates and coordinates the care of patients who are on research studies
- Experience: 2-3 years Clinical Nursing
- Licensure / Certification: Registered Nurse in the State of Ohio, Clinical resarch certified (CCRC), BLS/CPR (Basic Life Support for Healthcare Providers)
- Coordinate and conduct clinical research protocols in both the inpatient and outpatient CRCs including, but not limited to the following
- Effectively uses Microsoft computer software
Clinical Research Nurse
07/2011
-
04/2016
Boston, MA
- Demonstrates ability to coordinate and establish priorities among diverse tasks
- Set and meet deadlines; ability to maintain and organize multiple open clinical protocols
- Administers and implements treatment procedures or drugs, monitors and studies their effects, and conducts subject medical evaluations
- Attends research study or clinical trial related meetings, conferences and teleconferences, as well as participating in any additional planning and development related activities
- Work in conjunction with the endocrine disease team leaders, physician and scientific faculty, Cancer Center and research operations leadership to accomplish goals, projects and research initiatives for assigned disease teams
- Build and sustain relationships with internal and external stakeholders
- Manage and implement departmental programs and goals that support the strategic plan for the organization and for clinical research across COH
- Support departmental implementation of new technology, including EPIC and Oncore adoptions
Clinical Research Nurse, RN
06/2006
-
02/2011
Detroit, MI
- Prepare reports, presentations, action plans, and other deliverables
- Review reports submitted by staff members to recommend approval or suggest changes
- Effectively communicate (written & oral) across the organization
- Demonstrate the ability to develop processes to facilitate implementation of the research protocol to provide effective and safe medical research to all subjects
- Performs initial and ongoing assessments of research subjects and implements care directed towards optimal outcomes
- Appropriately and accurately assess potential subjects for inclusion and exclusion criteria
- Experience: 2-3 years Clinical Nursing. OB experience required
Education
Herzing University - Birmingham Campus
2001 - 2005
Bachelor's Degree in Nursing
Professional Skills
- Strong communication and interpersonal skills, along with the ability to work effectively as a member of an inter-disciplinary team
- Four years research nursing experience or four years of clinical nursing experience in a related specialty and two years of research nursing experience
- Four years research nursing experience orfour years of clinical nursing experience in a related specialty and two years of research nursing experience
- Excellent interpersonal, leadership, decision-making and issue resolution skills
- Management skills including experience of team leadership
- Strong written oral and communication skills
- Prior experience using the following computer programs: Midas and Apollo
How to write Clinical Research Nurse Resume
Clinical Research Nurse role is responsible for clinical, nursing, research, training, interpersonal, education, assessment, medical, basic, patient.
To write great resume for clinical research nurse job, your resume must include:
- Your contact information
- Work experience
- Education
- Skill listing
Contact Information For Clinical Research Nurse Resume
The section contact information is important in your clinical research nurse resume. The recruiter has to be able to contact you ASAP if they like to offer you the job. This is why you need to provide your:
- First and last name
- Telephone number
Work Experience in Your Clinical Research Nurse Resume
The section work experience is an essential part of your clinical research nurse resume. It’s the one thing the recruiter really cares about and pays the most attention to.
This section, however, is not just a list of your previous clinical research nurse responsibilities. It's meant to present you as a wholesome candidate by showcasing your relevant accomplishments and should be tailored specifically to the particular clinical research nurse position you're applying to.
The work experience section should be the detailed summary of your latest 3 or 4 positions.
Representative Clinical Research Nurse resume experience can include:
- Licensure / Certification: Certified Clinical Research Coordinator (CCRC), Registered Nurse in the State of Ohio and BLS/CPR (Basic Life Support for Healthcare Providers)
- Experience in working with changing priorities, frequent changes to protocols, occasional changes in research mission
- Related nursing experience and/or research nursing, OR a combination of education and experience
- Communicates effectively with volunteers and research team
- Collaborate effectively with program members and others outside of the program to meet research study, departmental and institutional objectives
- One or more years of RN experience in oncology and / or clinical research nurse experience
Education on a Clinical Research Nurse Resume
Make sure to make education a priority on your clinical research nurse resume. If you’ve been working for a few years and have a few solid positions to show, put your education after your clinical research nurse experience. For example, if you have a Ph.D in Neuroscience and a Master's in the same sphere, just list your Ph.D. Besides the doctorate, Master’s degrees go next, followed by Bachelor’s and finally, Associate’s degree.
Additional details to include:
- School you graduated from
- Major/ minor
- Year of graduation
- Location of school
These are the four additional pieces of information you should mention when listing your education on your resume.
Professional Skills in Clinical Research Nurse Resume
When listing skills on your clinical research nurse resume, remember always to be honest about your level of ability. Include the Skills section after experience.
Present the most important skills in your resume, there's a list of typical clinical research nurse skills:
- Strong written and verbal communication skills including computer skills are essential
- Prior experience in a position in which clinical skill and leadership qualities have been demonstrated
- Proven emergency care and comprehensive assessment skills
- Prior experience with lung function assessments, including spirometry, methacholine challenge testing, and sputum induction
- One or more years of clinical research nurse experience in solid tumor, medical oncology and / or Phase I. We are willing to train
- Cooperate and maintain a good rapport with nursing staff, medical staff, other departments, and visitors
List of Typical Experience For a Clinical Research Nurse Resume
1
Experience For Clinical Research Nurse Coordinator Resume
- Work independently with minimal supervision following Good Clinical Practice (GCP) guidelines
- Strong cardiology nursing background
- Valid CPR or BART certification
- Demonstrated ability to understand complex research protocols, including rationales for clinical/laboratory measurements and results
- Registered Nurse (RN) license issued by the state of California and six (6) months of clinical RN experience
- Knowledge of standard patient care equipment such as EKG, oximeter, blood pressure monitor, IV pumps, pipettes, centrifuge and ability to operate properly
- Provide care to study participants in compliance with the study protocol and within standards of Good Clinical Practice
- Maintains evidence-based standards of patient care
- Plans for and utilizes fiscal resources in a cost effective manner
2
Experience For Clinical Research Nurse Manager Resume
- Establishes, utilizes and maintains effective communication systems within the Research Network
- Working knowledge of databases, spreadsheets, and word processing software
- Working knowledge of computer applications such as CRF and EDC
- Willing to perform all tasks necessary to unit functioning and patient care
- Apply scientific principles to problem solving and to planning, providing and evaluating nursing care
- Assists with identifying toxicities and grade, using NCI Common Toxicity Criteria. Responds to and triages calls from patients regarding symptoms
- Assist in the management of patient files, copying and organizing research data
- Manage and coordinate intramural and extramural sites participating in clinical protocols for which the Principal Investigator is the coordinating center
3
Experience For Clinical Research Nurse, RN Resume
- Manage the implementation, tracking, data abstraction, collection, data reporting and coordination of a variety of Phase III clinical trials
- Assists with maintaining study forms/tools to facilitate accurate tracking and documentation of relevant study information
- Manages/oversees the dosing of Investigational Products given on the CRU during Phase I studies
- Responsible for scheduling of protocol visits and procedures, and providing reminder calls
- Has an opportunity to prepare and/or present data for publication/presentation and to participate in writing/editing manuscripts
- Completion of Collaborative Institutional Training Initiative (CITI) program training in information privacy security, HIPAA, and security and privacy
- Serves as clinical resource for triaging and addressing research related inquiries generated from websites and professional presentations
- Assist/train local study staff in explaining the protocol and tests/procedures to the study participants
4
Experience For Senior Clinical Research Nurse Resume
- Responsible for overseeing the direct patient care in a cardiac surgery intensive care unit for the care of non-human primates in a cardiac research model
- Coordinates the schedules of the OR and ICU nurses to ensure adequate staffing levels
- Serve as a liaison for hospital billing for research subjects
- Participate in promoting Human Subjects Protections within Clinical Research areas
- Independently coordinates one or more research studies or clinical trial protocols requiring the expertise and care of a Registered Nurse
- Assist with protocol-specific training for study personnel in preparation for study activities
5
Experience For Clinical Research Nurse Oncology Resume
- Evaluate adverse events and manage safety reporting in a timely manor
- Perform clinical procedures including blood draws, vital signs, drug administration, and specimen collection as outlined in the protocols
- Identify potential subjects from review of existing protected health information based on Inclusion/Exclusion criteria
- Coordinates and participates in site monitoring visits and audits
- Assist in the design of recruitment strategies. Recruit patients according to Institutional Review Board (IRB)/protocol approved methodologies
- Participates in the ongoing development, implementation, and evaluation of initiatives to enhance clinical research services and collaborations
- Provides patient consultation and education regarding clinical trials and provides study specific information when appropriate
- Monitor data collection by reviewing study data both independently and and resolve queries as needed
- Determine eligibility of subjects for assigned studies according to protocol
6
Experience For Clinical / Research Nurse, OB / GYN Resume
- Respond, lead and assist in emergency and code situations by following standard emergency protocols and SOPs
- Obtain and/or support informed consent from trial participants according to GCP guidelines and SOP’s, as required
- Expert knowledge and experience with standard patient care equipment such as EKG, oximeter, blood pressure monitor, IV pumps, phlebotomy, saline locks, assisting with various procedures, LPs, etc
- Knowledge of a broad range of medications, indications, dosage ranges, side effects, and potential toxicity including some exposure to current HIV, HBV, HCV, TB, and antibiotic medications
- Experience in recognizing adverse events in patients with complex disease processes such as HIV, HBV, HCV, TB, blood stream infections, respiratory infections, and other complex infectious diseases, and ability to communicate events to Admin Nurse and PI in a timely manner, ability to describe AE in detail both orally and written word
- Coordinate various activities to ensure proper and timely filing of serious adverse events, amendments, annual reports, and other regulatory documents
- Alert physicians of adverse events, abnormal outcomes or problematic trends, specifically in regards to protocol mandates
- Draft source documents to be used in new studies
7
Experience For Senior Clinical Research Nurse Coordinator Resume
- Provide assistance for all aspects of the protocol lifecycle including initial IND submission, IRB submission, continuing review applications, protocols, protocol amendments, annual reports, and protocol inactivation with IRB and FDA
- Complete flow sheets and case report forms according to the provisions of approved investigational protocols
- Create and maintain an IRB database of approved amendment descriptions
- Assist the Principal Investigator in data collection (including patient specimens) and data analysis; the writing of interim reports, annual protocol reports, and scientific publications; the interpretation of research data for the protocol team; and with performing site visits
- Coordinate Clinical Trial Agreement requirements with applicable Clinical Research Oversight Managers (e.g., safety reporting requirements) and data management, if data is to be provided to third party at end of trial. Follow up on monitoring reports to ensure that identified problems are adequately addressed and resolved
8
Experience For Clinical Research Nurse Coordinator Abdominal Transplant Resume
- Work with the Clinical Trials Management Clinical Research Oversight Manager to ensure consistency of case report forms with the management plan and coordinate site initiation and other monitoring site visits with all necessary parties
- Appropriately screen and collect blood samples from patients and donors
- Collaborate with the patient’s community physician and other health care providers to further the continuity of care and protect the integrity of the clinical research trial/data
- Develop patient rapport and assist in explaining the protocol and tests/procedures to the patients
- Maintain communication with the patient’s home physicians to ensure any ongoing home care is in accordance with the protocol guidelines
9
Experience For Clinical Research Nurse Supervisor Resume
- Conduct updates for clinical staff on patient care, protocol process and progress, human subject’s protection, ICH GCPs, and quality assurance education
- Confirm the collection of appropriate patient samples per protocol schema
- Consult with other health care professionals to meet medical, psychological and/or social patient needs
- Coordinate patient schedules and provide information for a successful visit to meet the required protocol procedures, data collection time points and nursing care
- Discuss toxicities experienced and drugs/dosages received by patient while at home
10
Experience For Clinical Research Nurse Translational Research Institute Orlando Resume
- Define, establish, and manage inclusion criteria such as patient population, diagnostic criteria, and patient condition
- Provide assistance in the management of patient data for the Protocol Chairman of a variety of clinical trials
- Recognize and support the needs of data integrity and retrieval, and interpret needs appropriately for Principal Investigators, patients and other staff members
- Recruit and enroll patients
- Assess, plan and follow up with disease-noted attributes
- Assist in the identification of the responsible party for data input into ClinicalTrials.gov at study conclusion, as applicable
- Participate in quality improvement and quality assurance initiatives involving database and data system development efforts as well as training programs for research nurses
- Collect and maintain current regulatory documentation from numerous ongoing clinical trials
List of Typical Skills For a Clinical Research Nurse Resume
1
Skills For Clinical Research Nurse Coordinator Resume
- Carrying out pre-screens efficiently and effectively to optimise patient recruitment
- Experience in providing a wide variety of patient care activities. Skill in coordinating clinical activities
- Demonstrated skill in using quality assessment and quality methods of nursing
- Prior experience in coordinating research trials
- Two years’ experience in managing all aspects of clinical research trials with in-depth knowledge of protocol requirements and Good Clinical Practice
- Strong working knowledge in Good Clinical Practice, FDA Code of Federal Regulations, and ICH guidelines
- Clinical nursing experience 2-3 years coordinator or related experience
- Prior experience using APeX
2
Skills For Clinical Research Nurse Manager Resume
- Clinical skills competency and laboratory processing competency
- Skill in excellent customer service and communication
- Comfort working with non-human primates (prior experience useful but not required)
- Interpersonal skills with ability to successfully interact with physicians, other medical providers and associates
- Working knowledge and understanding of regulatory compliance issues with respect to clinical trials and experience in adherence counseling techniques
- Promoting and nurtures a welcoming and pleasant environment for staff and participants to ensure effective team working, and provide professional leadership
- Nursing with previous oncology or clinical trial experience
- Nursing with previous diabetes or clinical trial experience
3
Skills For Clinical Research Nurse, RN Resume
- Working knowledge and skilled in use of Microsoft Office suite
- Working experience with regulatory and budgetary processes in clinical research
- Working knowledge applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP)
- Experience in a medical oncology setting or outpatient alcohol/drug addiction setting
- Experience working within a Clinic Setting
- Experience working in a large corporate or academic setting
- Experience as a clinical research coordinator and human subjects training certification required
- Thorough Knowledge of theory, practice, principles, processes and issues of nursing usually acquired through 2-3 years of clinical experience
- Experience, preferably in an academic medical setting
4
Skills For Senior Clinical Research Nurse Resume
- Previous working experience in research/clinical trials and/or HIV/AIDS or related specialty
- Licensed as a Registered Nurse in the state of Georgia and one year of related nursing experience
- Ideally some experience in working in a hospital
- RER - Demonstrates knowledge of federal and state regulations governing the participation of human and animal research subjects
- Experience working with inpatients with infectious complications
5
Skills For Clinical Research Nurse Oncology Resume
- Three (3) years recent acute experience in critical care nursing, to include the ICU, Cath Lab or Emergency Department
- Demonstrated willingness to strive for excellence with work processes and outcomes, honoring policies and regulatory requirements
- Experience coordinating human research protocols within the past 2 years
- Three years of nursing experience is required
- Nursing experience in a specialty area
- Experience in writing medical procedures
- Experience running Phase I clinical trials
- Licensed as a Registered Nurse in the state of Georgia and three years of related nursing experience
6
Skills For Clinical / Research Nurse, OB / GYN Resume
- Experience in a hematology or oncology setting
- Skilled in phlebotomy and blood sample processing
- Two or more years’ experience in Medical Oncology
- Two or more years’ RN experience with clinical research
- Demonstrated ability to use standard office equipment and software, including MS Office
- Experience working with HIV patients or on HIV related clinical trials
7
Skills For Senior Clinical Research Nurse Coordinator Resume
- Experience working within Orthopaedic surgical department or with Orthopaedic patients
- Oncology and regulatory experience
- Demonstrated clinical and management ability required
- Demonstrated ability to handle numerous simultaneous projects
- High attention to detail demonstrated in clinical and contractual settings
8
Skills For Clinical Research Nurse Coordinator Abdominal Transplant Resume
- Demonstrate vigilance in patient safety, protocol compliance, and data quality
- Keeping accurate records and updating forms to satisfy external funding agencies, NIH, FDA and OSHA regulations
- Confirming eligibility requirements for study participants, and enrolling and managing study participants as outlined by protocol guidelines
- Treating tobacco dependence, including use of FDA-approved medication for tobacco dependence, including Chantix (varenicline) and Zyban (bupropion)
- Promoting and nurturing a welcoming, professional and pleasant environment for staff and participants
- Attending all relevant meetings with veterinary and surgical services - Arranging and scheduling above meetings when necessary
- Assisting with the preparation of initial protocol budgets and being fiscally responsible for management of protocols
9
Skills For Clinical Research Nurse Supervisor Resume
- Assisting Principal Investigators with data collection, processing, compilation and analysis
- Purchasing and maintaining all equipment and supplies required for the research project
- Identifying opportunities to increase patient numbers, keeping aware of recruitment deadlines
- Adhering to NCSC’s and Nemours Research programs’ policies and procedures
- Assisting other research staff as appropriate
10
Skills For Clinical Research Nurse Translational Research Institute Orlando Resume
- Providing study relevant shift to shift information
- Issuing of Audit Reports on internal and external quality audit findings
- Initiating emergency action when required e.g. cardiac arrest, anaphylaxis management, fire, or critical incidents
- Providing health practices information and education to patients regarding medications, diseases, diet, exercise, and any special procedures
- Assisting patients by providing appropriate referrals to physicians, clinics, or agencies
- Acting as a liaison for patient/physician telephone calls
- Promoting and nurtures a welcoming, professional and pleasant environment for staff and participants
- Encouraging patients to continue within the study, and to participate in future trials
- Ensuring that all data queries are acted upon in a timely and efficient manner
List of Typical Responsibilities For a Clinical Research Nurse Resume
1
Responsibilities For Clinical Research Nurse Coordinator Resume
- Assist in the design of recruitment strategies. Recruit patients according to Institutional Review Board (IRB)/protocol approved methodologies. Using acceptable procedures, review records, identify and screen potential subjects to ensure they meet the study criteria
- Extract data from source documents. Complete Case Report Forms (CRF) or database entries. Audit for accuracy and correct CRFs. Resolve sponsor queries. Provide/create source documentation tools for subject’s charts/records
- Thorough knowledge, skill and ability to perform various medical and nursing procedures and to operate medical equipment
- Licensed as a Registered Nursein the state of Georgia and one year of related nursing experience
- Experience writing consents and protocols for IRB
- Experience in a healthcare setting preferably oncology or clinical trials (Required)
2
Responsibilities For Clinical Research Nurse Manager Resume
- Skill in ethically communicating risks and benefits to members of the Amish community
- Recent experience as a Clinical Research Coordinator
- Operate general office equipment: fax, printer and copier, required
- Experience in collaboration with medical and scientific investigators
- Preparing clinical equipment and areas, maintaining a safe environment for the
3
Responsibilities For Clinical Research Nurse, RN Resume
- Preparing ward areas for the study specific needs of the actual studies running in the ward
- Participating in multidisciplinary meetings
- Providing the volunteers with relevant plans, diary, forms for the assigned studies
- Exercise meticulous attention to detail when collecting, recording, safety reporting, and verifying study data, reviewing trends and share best practice
- Performs central line care including port and PICC flushing, dressing change, lab draws, and administering medications
- Prepares and adjusts recruitment and assessment study plans by designing strategies and analyzing data related to these components
- Performs data management activities including data abstraction, collection, source development and reporting
4
Responsibilities For Senior Clinical Research Nurse Resume
- Expertise in placing IVs, performing phlebotomy, and injections
- Ensures the coordination of scheduling of protocol related patient visits and required testing per the protocol calendar
- Management of CRF Shipment, Source Data storing and archiving after study finalisation
- Lab Specimen Handling Certification
- Reviews new patient records and screens patients for eligibility for participating in research protocol
- Manages all areas of clinical trials, including protocol development, regulatory submissions, and data management
- Develops administrative policies to ensure that staff are performing activities within established protocol, guidelines and federal regulations
- Provides immediate and urgent medical care to subjects experiencing medical complications
- Coordinates with pharmacy staff and dispensing of study medications. Assures proper documentation of medication dispensed
5
Responsibilities For Clinical Research Nurse Oncology Resume
- Participates in screening potential research participants for eligibility
- Facilitates the initial and ongoing informed consent or assent process
- Facilitates scheduling and coordination of study procedures
- Participates in study initiation, monitoring and close out visits
- Assists in providing resolution to participant inquiries and concerns
- Provides in-services and training to clinical staff in cross functional areas
- Manages sponsor interactions, including visits, queries and other requests
- Provides training to staff and acts as a mentor in research
- Review audit reports, complaints, initiating corrective and preventative action to ensure best practice
6
Responsibilities For Clinical / Research Nurse, OB / GYN Resume
- Chemotherapy teaching to include self-administration of injections and symptom management
- Monitor patients at home for anticipated chemotherapy/surgery/radiation-associated toxicities and screening for unanticipated toxicities
- MS in Nursing with oncology specialty and/or Oncology Nurse Certification
- Registration with no limitations to practice within the Nursing and Midwifery Council (Adult)
- Registration with no limitations to practice within the Nursing and Midwifery Council(Adult)
- An understanding of the research process
- One (1) year of acute care nursing
- Participates in continuing education, in-service programs and annual updates
7
Responsibilities For Senior Clinical Research Nurse Coordinator Resume
- Implements patient/family teaching when appropriate
- Some understanding of clinical research
- Assist in training new or temporary research staff
- Knowledge of the principles of aseptic technique and infection control including blood and body fluid precautions
- Graduate of NLN approved Nursing program, licensure as Registered Nurse by Board of Nurse Examiners for the State of Texas required
- Work under pressure and flexibility in working times
- Knowledge of ICH-GCP Guidelines and the PAREXEL internal Operating Procedures (SOPs)
- Motivational interviewing applied to health behavior change
- In oncology nursing
8
Responsibilities For Clinical Research Nurse Coordinator Abdominal Transplant Resume
- Nursing - Registered Nurse Required
- ONS Chemotherapy/Biotherapy certification , Human subjects protection training (can be completed after hire)
- Human subjects protection training (can be completed after hire)
- Coordinate the conduct of Phase II-IV clinical trials, including treatment, cancer prevention/control and cancer care delivery
- Contacts Study Sponsor appropriately regarding clarifications of eligibility, concomitant therapy, and/or query responses as necessary
- Prepares for and participates in quality assessment reviews (audits), including internal audits and Quality Improvement Projects
- Care and support of the volunteers participating in a study from admission to discharge
- Maintain a professional approach while maintaining patient confidentiality
- Knowledge of current research related policies and procedures as well as appropriate process for initiating revisions
9
Responsibilities For Clinical Research Nurse Supervisor Resume
- Current registered nursing license by State of Texas
- Licensed to practice professional nursing as a registered nurse (RN) in the Commonwealth of Massachusetts
- IATA Training and Certification
- Team player: current staffing has 2 RN’s, 1 MA and 1 BA (Business Mgr)
- Positive attitude, willing to cross-cover associates, problem solver
- Ethical and participant safety considerations. Maintain familiarity with the ethical conduct of research and safeguards needed when conducting research
10
Responsibilities For Clinical Research Nurse Translational Research Institute Orlando Resume
- CITI or equivalent clinical research certification
- Evaluating and enrolling patients in clinical research studies; Obtaining patients’ informed-consent, Collecting scientific samples and detailed, accurate data; Arranging follow up medical care to insure ongoing monitoring of patients in research protocols; Reporting adverse events to principal investigator and/or sponsor in a timely manner
- Carries out verbal or written Medical Orders (e.g., dose concomitant medications, closely monitor subject’s vital signs) as requested by the Investigator
- Responsible for the coordination of clinical research trials as assigned within the Neuro-Oncology section in the Division of Oncology and the Neurofibromatosis Program
- Participate in research team meetings, division-wide coordinator meetings and continued education and training within the CHOP Research Institute related to this role
- Adult Medication, , , , Peripheral IV Insertion and Maintenance
- Order and receive drug/device supplies. Dispense drug (calculate dosage as needed), supplies, and devices according to sponsor directions and institutional procedures. Provide clear instructions to the participants &/or their families. Ensure proper collection, documentation, processing and shipment of specimens
- Participates in clinical trial protocol development
- Develops procedure manuals for clinical trial protocols, 8) assists in the creation of case report forms
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