Clinical Research Associate Resume Sample
Wanda Jerde
5822 Dickinson Forges,
Phoenix,
AZ
+1 (555) 430 5967
Work Experience
Clinical Research Associate
08/2016
-
PRESENT
Philadelphia, PA
- Perform management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines
- Create phone scripts, questionnaires, and other assessment tools for use in the selection of sites
- Assist team in the development of site recruitment and retention strategy
- Initiate contact with Principal Investigators (PIs), schedule an conduct pre-visits, assess potential investigators and recommend suitability of the site
- Assesses data generated by R&D/Business Teams
- Assists Regulatory in preparing responses to regulatory agencies’ questions regarding the clinical study
- Serves as key contact to assigned clinical sites throughout the study process
Senior Clinical Research Associate
02/2011
-
06/2016
Detroit, MI
- Perform monitoring visits according to monitoring plan (including qualification visits, study initiation, training and closeout activities)
- Point of contact for sites and facilitator of communication between sites and key Edwards line functions
- Guide and support investigational sites on assigned projects
- Ensure preparation, collection and distribution of study master file documents
- Set up and ensure maintenance of investigator site file
- Timely write-up of study monitoring visit reports
- Support investigator in implementing appropriate contingency plans as needed
- Accountable for achieving and reporting on agreed clinical milestones
- Support study team in the interactions with Ethics Committees and Competent Authorities
Clinical Research Associate, Dermatology
01/2005
-
12/2010
Los Angeles, CA
- Participate actively to project team meetings, as required
- Assure continual compliance with ISO 14155 and Edwards SOPs in informed consent process, source data verification, AE and SAE reporting, protocol execution, accountability and other tasks as specified
- Resolve deviations to standard through remedial action and training
- Escalate any issues regarding study conduct to his/her manager as needed
- Provide information and documents for Data review, safety reporting and complaint handling, if required
- Supports training and mentor of new hire, if applicable
- Interface with CPM as necessary for successful trial execution. Support CPM in creation and preparation of appropriate study management tools
- Collaborate with monitoring team to coordinate on-site qualification, study initiation, interim monitoring and close-out monitoring visits at investigator sites as necessary to ensure study requirements are being fulfilled
Education
University of New Mexico - Taos Campus
1999 - 2004
Bachelor's Degree in Science
Professional Skills
- Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
- Strong communication skills, good presentation, negotiation and influencing skills
- Effective written and verbal English communication skills, strong oral presentation; interpersonal, decision making and issue resolution skills
- Professional collaboration skills, adept at influencing others and excellent communication skills
- Strong planning and organizational skills and the ability to work effectively and efficiently in adynamic environment with competing projects and deadlines
- Demonstrated initiative and excellent organizational skills in planning and executing study logistics
- Excellent oral and written communication skills. Ability to develop strong rapport with investigators and site staff
How to write Clinical Research Associate Resume
Clinical Research Associate role is responsible for english, interpersonal, organizational, computer, clinical, research, monitoring, technical, microsoft, organization.
To write great resume for clinical research associate job, your resume must include:
- Your contact information
- Work experience
- Education
- Skill listing
Contact Information For Clinical Research Associate Resume
The section contact information is important in your clinical research associate 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 Associate Resume
The section work experience is an essential part of your clinical research associate 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 associate 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 associate position you're applying to.
The work experience section should be the detailed summary of your latest 3 or 4 positions.
Representative Clinical Research Associate resume experience can include:
- Fluent in English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
- Good analytical and assessment skills, judgement, and problem solving skills
- Excellent interpersonal skills, including the ability to establish and maintain effective working relationships with customers, peers and stakeholders
- Use critical thinking skills to effectively solve problems and use conceptual thinking to anticipate impact of decisions
- Well organized, with good time management and prioritizing skills
- Demonstrated ability in positive relationship building, with strong verbal and written skills
Education on a Clinical Research Associate Resume
Make sure to make education a priority on your clinical research associate 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 associate 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 Associate Resume
When listing skills on your clinical research associate 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 associate skills:
- Excellent communication skills, including the ability to understand and present technical information effectively
- Effectively communicate using oral and written skills
- Demonstrates above average ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
- Demonstrate the ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
- Excellent computer skills and experience with MS Office programs
- A good team player, with strong inter-personal skills
List of Typical Experience For a Clinical Research Associate Resume
1
Experience For Senior Clinical Research Associate Resume
- Good oral and written communication skills, computer skills and experience with various data collection software
- Effective time management skills. Ability to effectively manage multiple priorities and responsibilities of increasing scope and complexity
- Excellent communication skills: written, verbal and presentation skills required
- Strong collaboration, co-creation and influencing skills demonstrated across different levels, functions and geographies
- Good IT skills in, e.g. MS Office, are essential, for planning, tracking, communicating and reporting
- Strong organizational and project management skills; - ability or aptitude to provide solutions and contingency plans through the comprehensive
- Strong analytical and conceptual capabilities, interpersonal skills, and ability to communicate with clarity. Ability
- Excellent oral and written communication skills, self-motivated, highly organized, and able to work independently in a fast-paced research environment
2
Experience For Lead Clinical Research Associate Resume
- Excellent computer skills (Microsoft Office Word, Excel, Outlook) required
- Effectively prioritizes work to meet deadlines
- Able to multi-task under limited direction and on own initiative. Strong communication and inter-personal skills
- Excellent written, listening, and verbal communication skills
- Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
- Good organizational and problem-solving skills
- Strong communication (verbal and written), negotiation and influencing skills
- Demonstrated computer skills (Word, Excel, PowerPoint, Outlook)
3
Experience For Clinical Research Associate, Dermatology Resume
- Demonstrates leadership skills, self-motivated and adaptable to a dynamic environment
- Driven self-starter with excellent self-management skills
- Solid interpersonal communication skills, both verbal and written
- Set and effectively communicate priorities in a dynamic environment
- Good coordination, organization and communication skills
- Demonstrate successful implementation of time management skills
- Strong organizational skills and attention to details required
- Able to work within teams and independently. Good interpersonal skills
- Good organizational, interpersonal and problem-solving skills
4
Experience For Lead Clinical Research Associate Amea Resume
- Strong written and verbal communication skills in applicable languages, and business level command of English
- Good written and verbal communication skills. Written and verbal fluency in
- Excellent organizational skills. Ability to manage time and work independently
- Strong interpersonal skills, ability to establish and promote positive business relationships,customer service oriented
- Effective leadership and cross-functional skills within a team
5
Experience For Associate Clinical Research Associate Resume
- Monitoring experience in clinical research or other Clinical research experience
- Exhibit competencies in analytical/decision making, planning/priority setting, effective communication, and driving innovation
- Language Skills Required: Speaking - English and Local Language; Writing/Reading: English and Local
- Language Skills Required: Speaking - English and Local Language; Writing/Reading: English and Local Language
- At least 12 months on-site monitoring experience, ideally including experience monitoring clinical trials in Australia or New Zealand
6
Experience For Field Clinical Research Associate, Spain Resume
- At least 12 months of on-site monitoring experience, including experience monitoring clinical trials in Australia or New Zealand
- Prior experience writing SOP’s, performing gap analyses of SOP’s to prepare for FDA audits
- BS or RN and 2 years of clinical research experience, some of which includes on-site clinical research monitoring experience
- Basic molecular biology research skills, including nucleic acid purification and manipulation
- Prepare and complete monitoring visit reports and letters, and effectively document site communications per the CMP
- Study design, planning, coordination, completion and analysis which provides the highest level of scientific evidence and effective outcomes
- Proven track record of developing strong relationships with internal and external stakeholders
7
Experience For Clinical Research Associate, Istanbul Resume
- Communicate and coordinate effectively with research teams and HSPB colleagues
- Experience in Clinical Research with progressive experience working in clinical trials
- Proven record of being customer driven and providing effective consultation and training
- Excellent working knowledge of International Conference on Harmonization/ Good Clinical Practice (ICH/GCP) regulations for sponsor study records
- Prior experience performing study start up activities (site qualifications, site initiations)
8
Experience For Clinical Research Associate, Korea Resume
- Work closely and effectively with all other department colleagues to ensure appropriate communication and study contact
- Knowledge and Skills in medical device and IVD industry, GCP and new product development
- A high level of both verbal and written communication skills
- Medical device industry experience as a CRA or experience in the medical device industry in either Clinical or Regulatory Affairs desired
- Communicate experimental results effectively in oral/written ways
9
Experience For Clinical Research Associate, Melbourne Resume
- Planning skills; ability to create and track detailed project plans
- Some prior Clinical Research Associate experience in Oncology
- Demonstrated effectiveness in resolving site management issues of varying complexity
- Experience hands-on clinical research experience encompassing all aspects of the clinical process, including
- Previous clinical research experience, including 2+ years of clinical site monitoring experience
- Strong experience managing early to late phases clinical studies and working with CROs and other study vendors
- Analyze,evaluate multiple solutions and solve complex problems using well developed critical & analytical thinking skills
10
Experience For Clinical Research Associate Cra-norway Resume
- Strong working knowledge of Good Clinical Practices (GCP) and FDA regulations related to clinical research
- Desired 4+ years experience in clinical research or having demonstrated adequate level of proficiency within the CRA II competency profile
- Experience in clinical research (monitoring) required, with experience in all stages of study lifecycle (start-up, recruitment and close out)
- Previous monitoring experience would be a strong asset
- Experience of clinical study monitoring or equivalent experience in the clinical research field is an asset
List of Typical Skills For a Clinical Research Associate Resume
1
Skills For Senior Clinical Research Associate Resume
- Demonstrated excellent written, verbal and organizational skills. Demonstrated ability to prioritize work, meet deadlines, and maintain accurate records
- Strong verbal and written communication skills and good interpersonal/group skills
- Excellent communication skills to effectively interact with all levels of administration and health care team
- Advanced verbal and written communication skills, in addition to excellent organizational skills and management of cross-functional teams
- Strong organization skills and ability to communicate effectively with and present to cross-functional groups
- + Good computer skills with good working knowledge of a range of computer packages
2
Skills For Lead Clinical Research Associate Resume
- Excellent communication and team work skills – in order to establish good communication line between PPD and the site
- Excellent communication skills (both written and oral) and the ability to build effective relationships
- Highly developed verbal and written communication skills, time management, and organizational skills
- Leadership and management skills to effectively assist with management of CROs and other vendors
- Proven interpersonal, leadership, organizational and effective time management skills
- Leadership skills, influence management and collaboration skills
3
Skills For Clinical Research Associate, Dermatology Resume
- Partnering with product managers to develop priority lists for clinical evidence and develop timelines for delivery of evidence
- Demonstrated ability to assist in the growth and development of project team members through mentoring and coaching and exhibiting leadership skills
- Strong organizational, writing and communication skills. Ability to prepare accurate, thorough and complete documents, including monitoring reports
- Strong organizational skills to cope with multi-tasking which result in a goal oriented approach without losing the attention to details
- Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadliness
- Strong working knowledge of ICH/GCP regulations and monitoring skills
- Demonstrate complex problem solving, decision making and communication skills
- Strong analytical and critical thinking skills to evaluate complex issues from multiple perspectives and drive smart decision making. Delete
- Excellent communication, interpersonal, decision making/problem solving and organizational skills
4
Skills For Lead Clinical Research Associate Amea Resume
- People management skills: good communicator in writing and verbally with the ability to speak assertively
- Have performed all visit types (site evaluation/selection, initiation, routine monitoring, and close-out)Demonstrated leadership skills
- Excellent writing skills and attention to project details
- Excellent computer skills, including proficiency with all office suite tools (MS Word, Excel, PPT, Visio)
- Proven planning skills; ability to create and track detailed project plans
- Detail savvy with excellent critical thinking skills
- Effective independent clinical monitoring skills
5
Skills For Associate Clinical Research Associate Resume
- Excellent communication skills (interpersonal, written, verbal, listening)
- + Good planning and organization skills
- Excellent computer skills in the following programs: MS Word, PowerPoint, Excel and Project
- Excellent written and oral communication skills including presentations
- Evidence of problem-solving skills
- Organizational, prioritization and time management skills
- Plans, Manages Time and Prioritizes Effectively
6
Skills For Field Clinical Research Associate, Spain Resume
- Good computer skills: Word, Excel, PowerPoint, Outlook
- Good English & communication skills
- Fluent written and verbal communication skills in Swedish including a good command of English language
- Strong communication skills, ability to influence others
- Exhibit good project management skills, the ability to multi-task and manage projects independently
7
Skills For Clinical Research Associate, Istanbul Resume
- Strong communication skills (both written and verbal) in both local language and English
- Interpersonal skills to develop/optimize strong site relationships
- Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility and
- Excellent communication, organizational skills, and attention to detail
- Excellent interpersonal skills, ability to elicit patient cooperation and work in interdisciplinary team harmoniously
8
Skills For Clinical Research Associate, Korea Resume
- Strong written and verbal English communication skills are essential
- Excellent written and verbal communication skills. Professional proficiency in both spoken and written English is required
- Strong written and verbal communication skills in applicable languages), and business level command of English
- Good organization skills; knowledge of GMP regulations
- Demonstrate technical expertise in computer skills and proficiency on all systems utilized by GSK throughout the lifecycle of a study
- Strong computer skills and the ability to quickly learn and utilize all systems as required by GSK throughout the lifecycle of a study
- Excellent interpersonal, judgment, and time management skills
- Demonstrated IT and administrative skills
- Excellent English & German language skills
9
Skills For Clinical Research Associate, Melbourne Resume
- Demonstrated skills in computers, communication, organization, and team effort
- Excellent organizationalskills. Ability to manage time and work independently
- Seeks out opportunities to demonstrate skills and knowledge base to senior
- Seeks out opportunities to demonstrate skills and knowledge base to senior leaders
- Communicate and work with international teams; good English skills, written and oral, required
10
Skills For Clinical Research Associate Cra-norway Resume
- Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with
- Effective oral and written communication skills in English and Dutch
- Strong communication and presentation skills; and
- Excellent organizational skills and be able to work on projects/tasks simultaneously
- Interpersonal, leadership, organizational and effective time management skills
- Excellent communication skills and independent, multi-tasking and collaborative in a cross-functional team
- Strong knowledge of GCP's, ICH guidelines and study management skills
- Effective interpersonal and written / verbal communication skills
List of Typical Responsibilities For a Clinical Research Associate Resume
1
Responsibilities For Senior Clinical Research Associate Resume
- Site management and site staff performance including monitoring all types of clinical trials ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
- Good computer skills on actual programs
- Communicating and coordinating effectively with research teams and HSPB colleagues
- Clinical trial experience in a pharmaceutical, biotechnology, CRO and/or healthcare setting (including 2+ years on-site monitoring experience)
- Prepares and completes monitoring visit reports and letters and effectively documents site communications
- Demonstrated experience performing site initiation visits, site qualification
- Prior experience reviewing Informed Consent Forms in order to obtain IRB approval
2
Responsibilities For Lead Clinical Research Associate Resume
- Experience in Clinical Research with progressive experience working in clinical trials
- Moderate experience as a CRA in directly relatable site management, or clinical site conduct experience
- Discretionary decision-making skills
- Two years of coordination of medical data experience or four years of RN experience required
- Communicate effectively, both written and orally cross-functionally - with colleagues, management and senior management
- Work effectively with patients, medical faculty and staff
- Effectively coordinates all functional areas involved in clinical trials to solve problems and assure progress and timely completion of study goals
- Clinical trial experience (CRO, healthcare settings and industry experience are acceptable)
3
Responsibilities For Clinical Research Associate, Dermatology Resume
- Experience in clinical research setting necessary, preferably with specific experience managing multicenter investigator-initiated trials
- Experience working in multi-site research studies requiring relationship management and prioritization
- Working knowledge of applicable clinical research principles and concepts, including Good Clinical Principles
- Monitoring experience in clinical development phase II-IV
- Understanding of FDA guidelines and regulations and principles of Good Clinical Practices (GCPs)
- Supporting site compliance with Good Clinical Practice (GCP)
- Solid understanding of clinical processes including clinical monitoring, data management, bio-statistics, medical writing, drug safety and regulatory affairs
- Excellent understanding of Clinical Study Management including monitoring, study drug handling and data management
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in France (1 year)
4
Responsibilities For Lead Clinical Research Associate Amea Resume
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in France (approximately 4 years)
- Clinical research independent monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
- Committee experience (CEC/DSMB/Steering)creating/leading independent physician committees
- Applies planning techniques for monitoring visits to ensure efficient and effective monitoring
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in Ukraine
- Clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
- Experienced with planning, directing, and coordinating projects
5
Responsibilities For Associate Clinical Research Associate Resume
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in Norway
- Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in Finland
- Experience in organizing and maintaining electronic filing systems for rapid, easy retrieval by self and others
- Experience with the development of protocols including formatting and preparation, ICFs, and study monitoring plans
- Previous clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits) in Belgium
6
Responsibilities For Field Clinical Research Associate, Spain Resume
- 27) Demonstrates a commitment toward meeting and exceeding the needs of our customers and consistently adheres to Customer Service standards
- Experience managing a core lab (Imaging, Echo or CT)
- Moderate practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
- Practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
- Demonstrates diligent and self-motivated approach to working in an off-site and independent working environment
- Relevant experience working in the pharmaceutical industry (including CROs, clinical sites, labs and biorepositories)
- Relevant technical experience working with biospecimen management, lab management, biobanking, or similar organizations
- Has a very good understanding and working knowledge of Clinical Study Regulatory requirements
- Experience developing Case Report Forms (CRFs), eCRFs, manual of operations and study monitoring plans
7
Responsibilities For Clinical Research Associate, Istanbul Resume
- Previous experience working in a healthcare setting required
- Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO in CNS area
- A good working knowledge of conducting clinical trials in general and specifically in oncology/ Medical Devices or Dermatology
- Experience in reporting and publishing clinical investigations within a medical environment
- Experience writing and maintaining SOPs
- Experience working in a clinical setting
- Experience with electronic or remote data capture monitoring as well as paper-based monitoring
- Collect and review of regulatory and site documents prior to study initiation and during study conduct
- 26) Demonstrates an understanding of the job description, performance expectations, and competency assessment
8
Responsibilities For Clinical Research Associate, Korea Resume
- Clinical research monitoring experience through a clinical research organization (CRO) or pharmaceutical company
- Practical experience with cell culture analytical equipment for all typical upstream unit operations used in biomanufacturing
- Excellent record keeping abilities to adequately record, analyze and document process development data
- Monitoring experience
- Experience running interventional clinical trials
- Demonstrated core understanding of medical terminology, medical records and clinical trial activities
9
Responsibilities For Clinical Research Associate, Melbourne Resume
- Previous pharmaceutical or medical device clinical study coordination, clinical site monitoring, or management experience required
- Extensive clinical monitoring experience
- Previous documented monitoring experience in clinical research
- At least 1.5 years’ monitoring experience in clinical development phase II-IV
- At least four years of on-site monitoring experience
10
Responsibilities For Clinical Research Associate Cra-norway Resume
- Successful completion of a CRA Trainee Program and at least one year of on-site monitoring experience
- On-site monitoring experience
- Off-site experience: familiarity with basic category of Clinical Monitoring Associate tasks
- As a clinical research associate, with diverse experience in all stages of study activity (start-up, monitoring and close-out)
- ICH-GCP experience and monitoring
- Knowledge of the dentistry sector and strong scientific understanding
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