Senior Clinical Research Resume Samples

4.5 (79 votes) for Senior Clinical Research Resume Samples

The Guide To Resume Tailoring

Guide the recruiter to the conclusion that you are the best candidate for the senior clinical research job. It’s actually very simple. Tailor your resume by picking relevant responsibilities from the examples below and then add your accomplishments. This way, you can position yourself in the best way to get hired.

Craft your perfect resume by picking job responsibilities written by professional recruiters

Pick from the thousands of curated job responsibilities used by the leading companies

Tailor your resume & cover letter with wording that best fits for each job you apply

Resume Builder

Create a Resume in Minutes with Professional Resume Templates

Resume Builder
CHOOSE THE BEST TEMPLATE - Choose from 15 Leading Templates. No need to think about design details.
USE PRE-WRITTEN BULLET POINTS - Select from thousands of pre-written bullet points.
SAVE YOUR DOCUMENTS IN PDF FILES - Instantly download in PDF format or share a custom link.

Resume Builder

Create a Resume in Minutes with Professional Resume Templates

Create a Resume in Minutes
SM
S Metz
Selena
Metz
933 Micaela Route
Dallas
TX
+1 (555) 873 7627
933 Micaela Route
Dallas
TX
Phone
p +1 (555) 873 7627
Experience Experience
Detroit, MI
Senior Clinical Research Professional
Detroit, MI
Roberts, O'Kon and Gibson
Detroit, MI
Senior Clinical Research Professional
  • · Provide psychosocial assessments of patients and families to identify emotional, social, and environmental strengths and problems related to their diagnosis, illness, treatment, and/or life situation
  • · Provide education and counseling to patients and families around issues related to adaptation to the patient's illness and/or life situation; may utilize crisis intervention, brief and long-term individual, group, and family therapies
  • · Provide therapy through face-to-face sessions, or telephone conferencing
  • · Liaison with community agencies; participate in area activities related to mental health
  • · Ensure that patient care documentation is timely, legible, and efficient. Documentation should be concise, pertinent, and meet the profession's and department's documentation standards. Oral reporting should be clear, concise, relevant, and timely
  • · Participate in staff meetings, quality improvement efforts, and make sure peer review standards are met
  • · Keep current with social work and health care developments and seek to increase further enhancement of job related knowledge
Chicago, IL
Senior Clinical Research Coordinator Licensed
Chicago, IL
Haley LLC
Chicago, IL
Senior Clinical Research Coordinator Licensed
  • Participate in conferences, meetings and seminars concerning research and surveillance projects to enhance knowledge base
  • Develop policies and procedures within area of responsibility
  • Assist with study start up and study closure activities such as site initiations and study close out conference calls and or site visits
  • May assist in the development of protocol defined data collection case report forms
  • Creates written reports of all monitoring activities to document on site visits including data integrity, newly discovered adverse events and follow action items through to resolution
  • Report directly to the Clinical Research Director with whom he/she will collaborate on the responsibilities for verification of data collection on grant-funded cardiovascular and neurovascular clinical trials
  • Participate in regular teleconferences and staff meetings
present
Chicago, IL
Senior Clinical Research Monitor Report Reviewer
Chicago, IL
Kovacek Group
present
Chicago, IL
Senior Clinical Research Monitor Report Reviewer
present
  • Compile information and provides status updates to monitoring management and to monitoring staff, as requested
  • Share review knowledge to monitoring management and monitors to initiate and/or support quality improvement efforts
  • Evaluate quality level of reports and letters in accordance with developed guidance
  • Provide technical support on systems to monitoring staff
  • May be involved in the start-up of new studies by providing input on the visit report template
  • Upon request create and deliver presentations on monitoring review activities
  • Provide training to monitors on monitoring visit report review processes and visit report completion issues, if requested
Education Education
Bachelor’s Degree in Relevant Technical
Bachelor’s Degree in Relevant Technical
University of Tennessee
Bachelor’s Degree in Relevant Technical
Skills Skills
  • Proficient knowledge of medical terminology, clinical practices, physiology and/or applicable disease states, RTG Implantable Therapies and technologies
  • Demonstrated ability to incorporate and adhere to Good Clinical Practices and regulatory standards
  • Proficient knowledge in word processing, spreadsheets, and/or database applications (e.g., MS Word and Excel)
  • Demonstrated ability to identify and adapt to shifting priorities and competing demands
  • Demonstrated ability to achieve objectives and milestones through identification and implementation of work plans and measurements
  • Demonstrated ability to clearly and effectively communicate verbally and in technical or scientific writing
  • Demonstrated ability to identify and implement solutions in addressing study issues
  • Demonstrated ability to maintain composure in difficult circumstances
  • Demonstrated ability to identify and overcome obstacles
  • Ability to constructively respond to feedback from customers and coworkers
Create a Resume in Minutes

15 Senior Clinical Research resume templates

1

Senior Clinical Research Mgr Resume Examples & Samples

  • 7 plus years experience managing multiple clinical research studies. Masters degree will substitute for 1 year of experience. PhD or MD will substitute for 2 years of experience
  • Experience managing medical device and/or pharmaceutical trials
  • 2 plus years clinical study personnel management (i.e., direct people management)
  • Experience with Good Clinical Practice (GCP) and regulatory compliance guidelines and regulations for clinical trials
  • Advanced degree (Masters, PhD or MD) preferred
  • Able to manage multiple tasks
2

Senior Clinical Research Monitor Report Reviewer Resume Examples & Samples

  • Perform review of reports in accordance to report review team guidance and expectations, along with monitoring plan requirements
  • Track processing time throughout review cycle
  • Evaluate quality level of reports and letters in accordance with developed guidance
  • Compile information and provides status updates to monitoring management and to monitoring staff, as requested
  • Partner in close collaboration with Lead Monitors
  • May be involved in the start-up of new studies by providing input on the visit report template
  • Upon request create and deliver presentations on monitoring review activities
  • Share review knowledge to monitoring management and monitors to initiate and/or support quality improvement efforts
  • Perform critical review of assigned Monitoring Action Item codes
  • Identification and escalation of protocol deviations, discrepancies in data, and non-compliance to study protocols, applicable regulations, Good Clinical Practices and Standard Operating Procedures
  • Understand the study protocol and accompanying study specific plans
  • Contribute to ongoing departmental, cross-functional and project-specific process improvement efforts
  • May create effective and efficient processes and systems for the review of monitoring visit reports
  • May work with study teams to prepare for internal or regulatory inspections
  • Provide technical support on systems to monitoring staff
  • Provide training to monitors on monitoring visit report review processes and visit report completion issues, if requested
  • Mentor, train and act as a resource to peers and/or junior personnel
  • Bachelor’s Degree with 4+ years of clinical research experience required
  • Bachelor’s Degree in life sciences, health related disciplines or Nursing preferred
  • Experience in CTMS and Oracle Clinical preferred
  • National or international certification (SoCRA, ACRP, etc.)
3

Senior Clinical Research Spec Resume Examples & Samples

  • Minimum 3 years experience directly supporting clinical research or research experience in medical/scientific area
  • Ability to independently oversee a study team and trial with little supervision
  • Understands databases, data analysis, and data presentation
  • Proficient knowledge of medical terminology, clinical practices, physiology and/or applicable disease states, aortic and/or peripheral vascular therapies and technologies
  • Good understanding of biostatistics and trial design
  • Working knowledge of Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials
  • Presents professional manner and appearance
  • Computer skills (MS Office products, word processing, spreadsheets, etc
4

Senior Clinical Research Spec Resume Examples & Samples

  • Minimum 4 years experience directly supporting clinical research or relevant experience in medical/scientific area
  • Experience with study management
  • Strong written, oral, and interpersonal communication skills
5

Associate Senior., Clinical Research Resume Examples & Samples

  • Ensures both regulatory and clinical protocol compliance is maintained for all assigned clinical projects
  • A Bachelor degree from an accredited university or college
  • An excellent understanding of all aspects of clinical research
6

Senior Clinical Research Spec Resume Examples & Samples

  • 2 years’ Project Management experience in a clinical setting
  • Strong knowledge of clinical monitoring functions and clinical research methodologies, including study design, implementation and reporting
  • Preferred education in engineering, life sciences or related medical/scientific field. Advanced degree preferred (Masters, MD, or Ph.D), RN preferred
  • Experience with Medical Device Industry Clinical Research
  • Work Experience directly supporting clinical research or similar experience in a medical/scientific area
  • Exposure to Clinical Operations
  • Demonstrated ability to work effectively on cross-functional teams. (Including R&D, Marketing, Operations)
  • Proficiency with writing reports, business correspondence and procedure manuals
  • Finance and budgeting knowledge
  • Knowledge of Diabetes
  • Advanced written and oral communications skills, with proficient knowledge of medical terminology
  • Ability to present complex technical products and processes to physicians in a clear, direct manner
  • High attention to detail and accuracy and ability to manage multiple tasks
  • Strong prioritization, organizational, and problem solving skills
  • Ability to work independently, with positive flexible outlook
  • Ability to present a professional manner and appearance
  • Experience with GCPs and regulatory compliance guidelines for clinical trials
7

Senior Clinical Research Mgr SH Resume Examples & Samples

  • Bachelor’s Degree in relevant biomedical field (Medicine, Biomedical Engineering, Medical Physics, Medical Biology, Health Sciences, etc)
  • Ph.D. or MD (will substitute for 2 years of experience)
  • Master’s Degree in relevant Biomedical field
  • Master of Business Administration
  • 10+ years experience directly supporting clinical research or similar experience in a medical/scientific area
  • 5+ years experience managing people, budgets and clinical studies across cultures and countries in Asia Pacific region
  • 3 – 5 years as a clinical research specialist
  • 3 – 5 years of medical device or pharma industrial experience
8

Senior Clinical Research Spec-erp Resume Examples & Samples

  • Bachelors degree and 4+ years clinical research experience to include study processes and study design; 2+ Years with Masters, or 0 with Doctorate
  • Experience as a clinical research specialist or customer specialist
  • Demonstrated ability to incorporate and adhere to Good Clinical Practices and regulatory standards
  • Proficient knowledge of medical terminology, clinical practices, physiology and/or applicable disease states, RTG Implantable Therapies and technologies
  • Project management capability
  • Ability to identify critical information needs and identify roles / individuals to involve for decision making within clinical studies
  • Demonstrated ability to identify and implement solutions in addressing study issues
  • Ability to identify customer requirements and manage expectations for clinical studies
  • Demonstrated ability to achieve objectives and milestones through identification and implementation of work plans and measurements
  • Demonstrated ability to clearly and effectively communicate verbally and in technical or scientific writing
  • Demonstrated ability to maintain composure in difficult circumstances
  • Demonstrated ability to identify and overcome obstacles
  • Ability to constructively respond to feedback from customers and coworkers
  • Proficient knowledge in word processing, spreadsheets, and/or database applications (e.g., MS Word and Excel)
9

Senior Clinical Research Data Specialist Resume Examples & Samples

  • Independently create CRFs (Case Report Forms) in electronic database systems to collect data from all clinical trials. The SCRDS ensures data collection is accurate, capturing all activities required by the protocol including, but not limited to all data groups such as: enrollment information, clinical labs/procedures, demographics, infusion information, response data, etc. The incumbent must be able to understand the needs of complex, high-risk, gene and immunotherapy clinical research protocols, and accurately build case report forms that capture required research information to ensure primary and secondary endpoints are captured
  • Continually evaluate the CRFs for required modification due to the dynamic nature of this research. Amend CRFs due to protocol amendments/changes in study endpoints
  • Oversee the development and review of study-specific data management documents, including Data Management Plans and Case Report Form Completion Guidelines, as well as sponsor data management standard operating procedures
  • Develop and conduct Investigator/Study Team training on the Clinical Database, CRFs, and data entry requirements
  • Provide input into study and project level data analysis plans
  • Participate in the preparation and presentation of study data/reports
  • Facilitate data cleaning activities including data review and query generation
  • Produce and provide metrics on data entry/processing to the Project Manager
  • Solve operational problems and be responsible for implementing process and system improvements
  • Coordinate the archiving of study data and study related documents
  • Interact with the Sponsor/Sponsor Program Managers, Project Managers, Monitors, Statisticians, Clinical Investigators, Clinical Cell and Vaccine Production Facility (CVPF), and Translational and Correlative Studies Lab (TCSL) to ensure required data is captured
10

Senior Clinical Research Budgeting Specialist Resume Examples & Samples

  • Experience in cost planning and Common Procedural Terminology (CPT) coding
  • Direct experience with budget negotiations experience a plus
  • Knowledge of federal regulations related to clinical research and billing compliance
  • Experience in healthcare compliance, general healthcare billing compliance, research billing, or research billing compliance
  • Knowledge of healthcare billing and claims processing a plus
  • Knowledge of Good Clinical Practice Guidelines, ICH Guidelines, FDA and HIPAA regulations
  • Experience working in an administrative/ business office of a university, hospital, or research institute
11

Senior Clinical Research Operations Specialist Resume Examples & Samples

  • Project management experience and/or day to day experience running clinical trials
  • Involvement in the development and/ or implementation of clinical research education and training
  • Implementation, workflow development and/or training with respect to an institution or company wide IT support systems (EPIC, document management systems, clinical trial management, electronic data capture systems, etc)
12

Senior Clinical Research Spec Resume Examples & Samples

  • 4+ years experience in clinical research (GCPs and regulatory compliance guidelines for clinical trials)
  • Bachelor’s degree in life sciences, engineering, or related medical/scientific field
  • Ability to manage multiple clinical research sites with proven results in study execution
  • Previous monitoring experience
  • Ability to shift priorities and work plan based on department needs
  • Excellent written and verbal communication skill
  • Capable of working on multiple projects in a deadline driven environment - demonstrated skill under pressure
  • Work effectively in cross-functional teams
13

Senior Clinical Research Operations Manager Resume Examples & Samples

  • Experience in project/program management in a clinical research environment
  • 5+ years progressive leadership experience
  • MBA or Masters Degree
  • Project Management Certification
  • Strong presentation skills, both delivery and development
  • Familiarity and experience with communications assessment techniques and tools
  • Previous experience working cross functionally in a matrixed organization
  • Experience implementing initiatives through effective influence management skills with those that have no direct reporting
14

Senior Clinical Research Coordinator Neurology Days Msh Resume Examples & Samples

  • Analyzes highly complex data gathered on clinical research studies
  • Coordinates protocols and human subject approvals between various sites
  • Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions, protocol amendments, and renewals of ongoing clinical trials
15

Senior Clinical Research Coordinator Pulmonary Critical Care Resume Examples & Samples

  • Must be proficient with Windows-style applications and keyboard, and various software packages specific to role
  • Proficient with Microsoft Office Suite
  • Ability to effectively work indepdently
  • Ability and willingness to learn and apply new techniques
  • Reliable transportation to travel across the system
16

Senior Clinical Research Coordinator Pain Management Resume Examples & Samples

  • Nine years relevant research experience; or six years of research experience in a clinical setting with a Bachelor of Science degree
  • Current Basic Life Support (BLS) certification from teh American Heart Association
  • Must have computer skills and dexterity required for data entry and retrieval of required job information
  • Effective verbal and written communication skills and the ability to present information clearly and professionally to varying levels of individuals throughout the required job processes
  • Working knowledge and experience in clinical research
  • Ability to work flexible hours, when applicable
17

Senior Clinical Research Coordinator Licensed Resume Examples & Samples

  • Report directly to the Clinical Research Director with whom he/she will collaborate on the responsibilities for verification of data collection on grant-funded cardiovascular and neurovascular clinical trials
  • Responsible for independently scheduling site monitoring (Review source documentation, case report forms, electronic date entered and data reports for accuracy and ensure the timely submission of such documentation) to assure compliance with the protocols, investigational plans, monitoring plans, applicable regulatory, IRB standards, guidelines and policies. While onsite, will review all trial device and/or product accountability as necessary
  • Creates written reports of all monitoring activities to document on site visits including data integrity, newly discovered adverse events and follow action items through to resolution
  • Assist with study start up and study closure activities such as site initiations and study close out conference calls and or site visits
  • Assist with compilation of adverse events, source documentation and preparation for Event Adjudication Committee meetings as needed
  • May assist with data management activities for clinical studies, as required
  • May assist in the development of protocol defined data collection case report forms
  • Develop policies and procedures within area of responsibility
  • Participate in conferences, meetings and seminars concerning research and surveillance projects to enhance knowledge base
  • Participate in regular teleconferences and staff meetings
  • Timely responses to site questions are imperative, therefore personal digital assistant (e.g., Blackberry) will be provided
  • Mentors, trains and reviews the work of less experienced clinical research monitoring staff
  • Perform other related duties
18

Senior Clinical Research Assoicate Resume Examples & Samples

  • Must possess 4+ years of oncology experience
  • A minimum of four (4) years of monitoring/site management experience is required
  • Must be able to travel domestically and internationally approximately 65%-85%
19

Senior Clinical Research Professional Resume Examples & Samples

  • · Provide psychosocial assessments of patients and families to identify emotional, social, and environmental strengths and problems related to their diagnosis, illness, treatment, and/or life situation
  • · Provide education and counseling to patients and families around issues related to adaptation to the patient's illness and/or life situation; may utilize crisis intervention, brief and long-term individual, group, and family therapies
  • · Provide therapy through face-to-face sessions, or telephone conferencing
  • · Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations
  • · Maintain knowledge of external resources for patient needs to foster recovery
  • · Liaison with community agencies; participate in area activities related to mental health
  • · Manage department appointment schedules as appropriate
  • · Ensure that patient care documentation is timely, legible, and efficient. Documentation should be concise, pertinent, and meet the profession's and department's documentation standards. Oral reporting should be clear, concise, relevant, and timely
  • · Perform all required data collection for the department and grant requirements accurately and within expected time frame
  • · Participate in clinical supervision as needed on a scheduled basis
  • · Maintain current licensure, participate in continuing education, and meet competency skills for evaluations in area of practice
  • · Maintain knowledge of and compliance with HIPAA policies, documentation guidelines, and other related regulatory requirements
  • · Participate in staff meetings, quality improvement efforts, and make sure peer review standards are met
  • · Keep current with social work and health care developments and seek to increase further enhancement of job related knowledge
  • · Provide education to other health care professionals as needed
  • · Perform other duties as assigned
  • Licensed Independent Social Worker with current credentials to practice in the state of Ohio
  • Master’s degree or doctorate in social work
  • Minimum 2 years previous supervised social work experience preferred
  • Proficiency in various computer and software applications preferred
  • Previous experience in Continuous Quality Improvement activities preferred
  • HIV experience strongly preferred but not required
20

Senior Clinical Research Analyst Resume Examples & Samples

  • Serve as an analytic resource within multi disciplinary project teams
  • Conduct ad hoc analyses of data as requested by hospitals, clinicians, and internal customers
  • May work focus on more complex project
  • Ability to work proficiently with Microsoft Word, Excel, Access, DB2, and SQL
  • Ability to demonstrate strong time management and project management skills
  • Strong with customer-service orientation
  • Ability to be careful and thorough about detail
  • Ability to perform well in team environment, with employees at all levels, to achieve business goals