Senior / Clinical Research Associate Resume Samples

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JC
J Cormier
Jessie
Cormier
217 Roob Fall
Detroit
MI
+1 (555) 586 6692
217 Roob Fall
Detroit
MI
Phone
p +1 (555) 586 6692
Experience Experience
08/2015 present
Detroit, MI
Senior Clinical Research Associate, Oncology
Detroit, MI
Senior Clinical Research Associate, Oncology
08/2015 present
Detroit, MI
Senior Clinical Research Associate, Oncology
08/2015 present
  • Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA
  • Manage specific study responsibilities as assigned by Sr. Manager or Clinical Operations Director/Sr. Director
  • Assist with management of third party vendors
  • Assist in the development, assembly and distribution of study documents, manuals and tools
  • Assist the study management in identifying and generating changes in scope
  • Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
08/2011 03/2015
Los Angeles, CA
UK Senior Clinical Research Associate
Los Angeles, CA
UK Senior Clinical Research Associate
08/2011 03/2015
Los Angeles, CA
UK Senior Clinical Research Associate
08/2011 03/2015
  • Develop new improved processes and perform implementation
  • Provide field training and guidance to new Clinical Specialists
  • Assist and conduct Clinical Monitoring activities
  • Data review, safety reporting and complaint handling
  • Collecting completed Case Report Forms (CRF) and collecting, confirming and auditing supporting documentation
  • Document procedural case observations for insights in investigating post procedural events
  • Ensures Audit readiness for internal, external and site Audits
12/2004 05/2011
Chicago, IL
Senior.clinical Research Associate
Chicago, IL
Senior.clinical Research Associate
12/2004 05/2011
Chicago, IL
Senior.clinical Research Associate
12/2004 05/2011
  • Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work
  • In country based, may provide administrative management oversight to up to 8 Study Leads responsible for conduct of study at local level
  • Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested by Clinical Trial Manager
  • Informs the Clinical Operations Manager and/or the Senior Clinical Operations Manager of any variance
  • Provides coaching, counseling, and feedback, and identifies developmental opportunities for assigned staff
  • Track and manage performance metrics for assigned monitoring staff
  • Assists in resolving any issues in order to ensure compliance with site file audits in conjunction with ISSC
Education Education
Bachelor’s Degree
Bachelor’s Degree
University of San Francisco
Bachelor’s Degree
Skills Skills
  • Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software
  • Excellent understanding and demonstrated application of GCPs and applicable SOPs
  • Strong attention to detail
  • Excellent English and Spanish skills
  • Willingness and ability to travel
  • Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
  • Strong customer focus
  • Proven flexibility and adaptability
  • Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
  • Development and preparation of the local informed consent form
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15 Senior / Clinical Research Associate resume templates

1

Senior Clinical Research Associate, R&D Resume Examples & Samples

  • Set up the GCP infrastructure necessary to conduct simple in-house clinical studies such as method comparison and precision
  • Write and maintain necessary SOPs, study binders and personnel training records that are required to be in compliance with GCP
  • Help develop and implement specifications, SOPs and plans for electronic data capture, data management and statistical analysis of clinical data that meet GCP and project requirements
  • Work with external vendor and project team to configure, test and implement eDC system as per specifications
  • Help qualify, initiate and audit external CROs conducting clinical studies to ensure they meet GCP and company requirements
  • Help monitor ongoing clinical studies including monitoring data collection, patient sample usage and testing supplies usage
  • Work with partners to resolve issues and escalate to management issues that can impact study timing and quality
  • Help develop and execute procedures to close clinical studies and reconcile clinical samples, supplies and data
  • B.S. in Biology, Medical Technology, Clinical Laboratory Science, Chemistry, Biochemistry, Biotechnology or related scientific or engineering discipline
  • A minimum of 5 years experience in Clinical Affairs preferably in the In-Vitro Diagnostics (IVD) medical device industry
  • Thorough understanding of FDA, ICH and GCP regulations, requirements and guidance for IVD device validation and clinical studies in support of 510k applications including clinical data management, electronic data capture (eDC) and clinical site initiation, monitoring and closing
  • Strong written and verbal communication skills and ability to work effectively across functions and sites
  • Ability to work independently and build organizational capabilities and processes from the ground up
  • This position does not offer Relocation Assistance
2

Senior / Clinical Research Associate Resume Examples & Samples

  • Solid regulatory and ethics knowledge of Israel
  • Valid passport
  • Experience as a Clinical Research Associate / monitor or in a health sciences field / clinical research setting is preferred
3

Senior / Clinical Research Associate Portugal Resume Examples & Samples

  • In depth knowledgee of ICH-GCP, EU and FDA requirements
  • Experience of clinical trials in Portugal
  • Experience in Oncology (preferably Melanoma or lung)
  • Excellent English and Portuguese skills
  • Previous xperience in the CRO industry would be advantageous
4

Senior / Clinical Research Associate, Ukraine Resume Examples & Samples

  • You will perform and coordinate all aspects of the clinical monitoring process from "start up" to "close out"
  • You should thrive in multi-national project teams and be focused on delivering exemplary levels of customer service
  • Degree in medical science, pharmacy, life science or related field
5

Senior Clinical Research Associate Based Resume Examples & Samples

  • Several years of monitoring experience
  • Excellent English
  • Willingness & ability to travel
  • Flexibility and ability to work on multiple projects and to support tasks such as feasibilities, site contracts and budgets, submission documentation and contribute to regulatory country intelligence as required
  • Experience of starting up clinical studies or contributing to start up tasks
6

Senior / Clinical Research Associate Resume Examples & Samples

  • A minimum of 2 years on site monitoring experience
  • Experience of clinical trials in Spain
  • Excellent English and Spanish skills
  • LI-EC1
7

Senior Clinical Research Associate CPS Resume Examples & Samples

  • Function as a mentor and role model for other CRA team members
  • Provide study specific training for CRAs acting as a lead CRA on individual projects
  • Establish site recruitment plan in collaboration with site during qualification visit; follow-up and update at initiation visit and monitoring visit
  • Attend external client meetings and presentations including investigator meetings and professional conferences
8

Senior Clinical Research Associate Permanent Resume Examples & Samples

  • Conducting feasibility
  • Set up of our Insourced Clinical Trials. Includes HRA/Ethics submissions, budget negotiations and creation of monitoring tools
  • Perform all types of site visits including qualification visits, initiation visits, monitoring visits, motivational visits and close out visits to ensure patient safety and data integrity
  • Train and assist investigative sites
  • May assist/take on monitoring lead activities for a Global study as needed
  • Identify/evaluate potential investigators for future Celgene studies
  • Establishing/maintaining a local partnership with our Partner CROs
9

Senior / Clinical Research Associate Resume Examples & Samples

  • Oversees the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements
  • Administer protocol and related study training to assigned site
  • Establish regular lines of communication with sites to manage ongoing project expectations and issues
10

Senior / Clinical Research Associate Resume Examples & Samples

  • A minimum of 24 months on site monitoring experience
  • In depth knowledge of ICH-GCP and FDA requirements
  • Experience of clinical trials
  • Willingness and ability to travel across Africa
  • Excellent Portuguese and English language skills
11

Senior.clinical Research Associate Resume Examples & Samples

  • Participates in the investigator recruitment process. Performs initial qualification visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study, both clinically and technically
  • Assists in the preparation and review of protocols, eCRFs, study manuals, and other study documents as requested by Clinical Trial Manager
  • Works with the Study Start-up Group to coordinate activities with the site in preparation for the initiation of studies. Obtains and reviews regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with Study Start-up Group and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
  • Serves as mentor for more junior CRAs as well as new CRAs to the project
  • May conduct field training and assessment of CRA Is and CRA IIs
  • Strong knowledge of clinical research process and medical terminology
  • Ability to handle several priorities within multiple, complex clinical trials
  • Willingness and ability to travel domestically and internationally, as required
12

Senior Clinical Research Associate Quebec & Eastern Territory Resume Examples & Samples

  • Investigative Site Monitoring -Demonstrate a commitment to quality in all aspects of monitoring; adhere to study monitoring plans; conduct Pre-study Visits at Investigative Sites; conduct Study Initiation Visits at Investigative Sites; conduct Interim Monitoring Visits at Investigative Sites; review investigator study files and reconcile versus trial master files; perform investigational product accountability; conduct Close-out Visits at Investigative Sites
  • Train and Assist Investigative Sites- Attend Investigator Meetings; train investigative site personnel in GCP and ensure sites are conducting Celgene clinical research according to the protocol, local regulatory requirements, and other appropriate regulations; serve as the liaison between Celgene and assigned sites; build relationships with site staff at assigned sites
  • Communication- Identify site issues, ensure proper escalation, if necessary, and ensure resolution; create trip reports, confirmation/follow-up correspondence and telephone contacts for assigned sites; respond to audit findings; adhere to proper lines of communication within Celgene; attend and participate in study team meetings; keep information in the CTMS current; maintain calendar
  • Development -Maintain up-to-date medical and clinical knowledge for assigned therapeutic areas; mentor/coach new CRAs; maintain annual training records
  • Significant knowledge of Clinical Development Process
  • Knowledge of regulatory environment and guidelines (ICH, GCP and CFR)
  • Excellent relationship-building skills
  • Bilingual in English and French a requirement
  • LI-TS1
  • LI-PRIORITY
13

Senior Clinical Research Associate, Virology Resume Examples & Samples

  • Relevant experience in multi-therapeutic indications as they relate to the conduct of clinical trials
  • Experience within AbbVie Clinical Operations department by working on global clinical studies in an affiliate is a definite key asset
  • Experience monitoring virology studies is desired
14

Senior Clinical Research Associate UBC Resume Examples & Samples

  • Monitors clinical trials to ensure investigator and sponsor responsibilities are compliant with regulatory requirements
  • Attends project team meetings, department meetings and minimum of monthly 1:1 with manager; responsible for content of these meetings
  • Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to CSS/RDS for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal corrections
  • Ensures completion of Call Log or Telephone Contact Report detailing communication with sites per protocol
  • Monitors within EDC data entry, if applicable, and assists sites with DCF resolution
  • Maintains regular contact with assigned sites per study requirements
  • Consistently submits expense reports within UBC timelines; consistently follows UBC Travel Guidelines
  • Consistently completes sponsor specific training and documentation within requested timelines
  • Instruct how to conduct visit, report/letter writing and manage issues and actions
  • Bachelor’s degree – Life Science preferred or equivalent years of industry and monitoring experience
  • Thorough knowledge of medical terminology
  • Consistently meets or exceeds metrics for quality trip reports and letters
  • Consistently meets or exceeds metrics for completion of UBC and/or sponsor training with appropriate documentation
  • Thorough knowledge of ICH, GCP, CFR and UBC SOPs
15

Temporary Senior Clinical Research Associate Resume Examples & Samples

  • Associates Degree within healthcare or life science discipline or licensed professional (e.g, RN) required; Bachelor’s degree preferred
  • Minimum 3 years prior experience as CTA or comparable work experience in the field of research/development in an administrative capacity required; Field CRA experience, certification as a CCRA/CCRC/CCRP, or completion of a recognized clinical research certificate/training program is a plus
  • A demonstrated understanding of ICH-GCP, including the ability to recognize deficiency and recommend corrective actions
  • Basic understanding of medical terminology
  • Proficiency with Microsoft Outlook, Excel, Word and PowerPoint is required; proficiency with clinical software systems (e.g., CTMS, IXRS, EDC) is a plus
  • Effective communication skills with the ability to vary writing style to connect with different audiences
  • Basic math skills along with the ability to compute rate, ratio, and percent
  • Ability and desire to work in a team environment
  • Proven ability to work independently and effectively handle multiple priorities in a fast-paced environment
16

Senior.clinical Research Associate Resume Examples & Samples

  • Train site staff on the EDC system and verify site computer system
  • Assure adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures through on-site monitoring visits. Performs validation of source documentation as required by sponsor. Prepares monitoring reports and letters per the timelines defined in Novella SOPs by using approved Novella/sponsor templates and reports
  • Review the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Work with sites to resolve data queries
  • May review draft protocols, eCRFs, monitoring reports and follow-up letters, study manuals and other prepare study-related documents and templates, as requested by the CTM and/or PM
  • May serve as primary contact between Novella and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested
  • Ensure all study deliverables are completed per Novella and study timelines
  • Perform other duties, as requested
  • Four+ years of oncology experience and/or medical device
  • Understand electronic data capture including basic data processing functions
17

UK Senior Clinical Research Associate Resume Examples & Samples

  • Support implementation of assigned clinical research projects in Europe related to specific products/topics according to internal and external regional requirements, including acquisition of human use approval from Ethics Committees, case report form review, data collection, site monitoring and auditing. Maintains close contact with clinical study site coordinators and physicians who are clinical investigators
  • Supervises, leads and motivates study sites
  • Ensures Audit readiness for internal, external and site Audits
  • Develop new improved processes and perform implementation
  • Provide field training and guidance to new Clinical Specialists
  • Reporting site enrollment progress including device accountability and enrollment deviations (inclusion/exclusion criteria, sequential enrollment)
  • Assist and conduct Clinical Monitoring activities
  • Or equivalent in related field
  • 5 years of
  • Of previous related medical
  • Device and/or clinical
  • Experience or
  • Clinician experience in intraoperative
  • Procedures acquired
  • From Registered Nursing
  • Degree curriculum (RN), or in
  • Positions such as Radiologic
  • Technologist (RT), Operating
  • Room Technician (ORT), or
  • Cardiovascular Technician
  • (RCIS) or
  • Experience in interventional
  • Cardiology or cardiothoracic
  • Surgery
  • Strong written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills
  • Full knowledge and understanding of cardiovascular science
  • Full understanding of cardiovascular anatomy, pathology and physiology
  • Full understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
  • Must be able to work in a team environment, including inter-departmental teams and key contact representing the organization on contracts or projects
  • Ability to interact with senior internal and external personnel on significant matters often requiring coordination between organizations
18

Senior Clinical Research Associate, Oncology Resume Examples & Samples

  • Document accountability, stability and storage conditions of clinical trial materials as required by sponsor. Performs investigational product inventory. Ensures return of unused materials to designated location or verifies destruction as required
  • Ensure internal and study-related trainings are completed per Novella and/or study timelines; CTMS should be current at all times with the pertinent site updates/contacts
  • May conduct Field Evaluation Visits and field training of CRA Is, IIs and Sr CRAs
  • Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA
  • Able to mentor other CRAs and co-monitor, as required
  • Ability to travel domestically and internationally
19

Senior Clinical Research Associate, Oncology Resume Examples & Samples

  • Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready
  • Minimum of 4 years of direct site management (monitoring) experience in a Biopharmaceutical, Pharmaceutical or CRO company
  • Experience monitoring Oncology clinical studies
  • Fluent in Local Languages and English (verbal and written) and excellent communication skills, including the ability to understand and present technical information effectively
  • Excellent understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines
  • Excellent understanding of Global, Country/Regional Clinical Research Guidelines and ability to work within these guidelines
  • Demonstrated ability to mentor/lead
  • Proven Skills in Site Management including independent management of site performance and patient recruitment
  • High sense of accountability / urgency. Ability to set priorities and handle multiple tasks simultaneously in a changing environment
  • Demonstrates commitment to Customer focus
  • Works with high quality and compliance mindset
20

Senior Clinical Research Associate Level Resume Examples & Samples

  • Understanding of ICH-GCP, EU and FDA requirements
  • Fluency in English and in Russian
  • Proven clinical monitoring skills
21

Senior.clinical Research Associate Resume Examples & Samples

  • Provides leadership and oversight for activities undertaken by Clinical Operations (CO) Site Management & Monitoring personnel in charge of implementing and monitoring clinical studies conducted within country (ex-US)/ region (US) of responsibility
  • In country based, may provide administrative management oversight to up to 8 Study Leads responsible for conduct of study at local level
  • Accounts for complexity of site and study issues
  • Trains assigned personnel in monitoring techniques and study-specific requirements also through accompanied on site visits. Functions assigned staff as a resource for monitoring-related questions and gives appropriate guidance
  • Responsible for reporting within company systems of Site Management & Monitoring headcounts/resources/workload planning and actuals in country(ies)/region(s) responsible for
  • Trains personnel in monitoring techniques and study specific requirements also through accompanied on site visits. Functions as a resource for monitoring-related questions and gives appropriate guidance. Trains personnel on country specific regulation/processes/procedures (ex-US)
  • Advises on pre-audit activities for both PV and GCP requirements
  • Supports the Clinical Operations Manager and/or Senior Clinical Operations Manager in the development and implementation of site management initiatives to maintain enrollment and recruitment timelines
  • Reviews monitoring visit reports for assigned SCRAs
  • Endures corrective action is implemented at the clinical site if appropriate
  • Where appropriate, monitors project progress against time frame and budget
  • Informs the Clinical Operations Manager and/or the Senior Clinical Operations Manager of any variance
  • Proven strong site management and monitoring skills in Neurology
  • Strong planning and organizations skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines. Demonstrated ability to manage multiple priorities/projects
  • Excellent communication and interpersonal skills, including situations of conflict resolution, problem solving and crisis management
  • Demonstrated proactive and positive team player
  • Exhibits high level of flexibility when facing changes in the work environment
  • Working knowledge and experience in AbbVie systems (electronic data capture systems and clinical trials management systems) and procedures are desirable
22

Senior Clinical Research Associate Ontario Territory Resume Examples & Samples

  • Data Integrity -Conduct Source Document Verification of CRFs against medical records to ensure CRFs are a valid representation of the subjects during their participation in a study; evaluate data query trends and interact with study team in order to improve data quality; ensure issues of data quality are escalated and resolved with study team and CQA
  • Subject Safety- Perform safety reviews/SAE reconciliations; monitor the informed consent process; ensure investigative sites’ adherence to GCP, ICH guidelines, and local regulations
  • Corporate Goals- Identify/evaluate potential investigators for future Celgene studies; build effective and positive relationships with Principal Investigators; ensure timely submission and review of CRF data and query resolution according to timelines set forth in the SMP; schedule travel following Celgene’s travel policy, and submit expense reports in an accurate and timely manner
  • Regulatory Documentation -Prepare ethics submissions and local regulatory documents at the country level, as needed; maintain local document files at a country level, as needed; review translations for ICD and other study documents, as needed; oversee to assure SOPs are followed in obtaining translations on necessary study documents
  • Monitoring Lead (As assigned)- Serve on study team as monitoring representative; review RFPs regarding monitoring specifications; develop the study monitoring plan and subsequent revisions; review, track and acknowledge monitoring visit reports; manage and track monitoring site visits to ensure quality monitoring; ensure adequate monitoring resources; ensure monitors are trained properly in the study requirements; track and report critical issues to study team; participate in CRF and protocol review process; attend, participate and present at Investigator Meetings; perform field assessments of Celgene and CRO FMs, as required; develop study-specific tools for Investigative sites and Field Monitors; conduct FM meetings; oversee CRO monitoring, as required
  • Expert in a number of diseases, treatments, and compounds
  • Experience with developing study monitor plans
  • Significant site management skills
  • Excellent written and oral communication skills, including presentations
  • Proficient in writing function SOPS / Work Practices Demonstrated problem-solving skills
  • Ability to resolve routine issues effectively and independently
  • Organizational and time management skills
23

Senior.clinical Research Associate Resume Examples & Samples

  • Ensure adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring Plans, and to quality standards in conducting clinical research. Stay abreast of new and/or evolving local regulations, guidelines and policies
  • Ensure audit and inspection readiness of assigned sites. Advise on pre-audit activities for GCP requirements. Prepare and follow up site audits/inspections; provide input into the CAPA preparation
  • Responsible for coaching and mentoring CRAs and providing input into their development. Responsible for mentoring CRAs for various aspects of work
24

Senior Clinical Research Associate Western Resume Examples & Samples

  • Investigative Site Monitoring - Demonstrate a commitment to quality in all aspects of monitoring; adhere to study monitoring plans; conduct Pre-study Visits at Investigative Sites; conduct Study Initiation Visits at Investigative Sites; conduct Interim Monitoring Visits at Investigative Sites; review investigator study files and reconcile versus trial master files; perform investigational product accountability; conduct Close-out Visits at Investigative Sites
  • Data Integrity - Conduct Source Document Verification of CRFs against medical records to ensure CRFs are a valid representation of the subjects during their participation in a study; evaluate data query trends and interact with study team in order to improve data quality; ensure issues of data quality are escalated and resolved with study team and CQA
  • Subject Safety - Perform safety reviews/SAE reconciliations; monitor the informed consent process; ensure investigative sites’ adherence to GCP, ICH guidelines, and local regulations
  • Train and Assist Investigative Sites - Attend Investigator Meetings; train investigative site personnel in GCP and ensure sites are conducting Celgene clinical research according to the protocol, local regulatory requirements, and other appropriate regulations; serve as the liaison between Celgene and assigned sites; build relationships with site staff at assigned sites
  • Communication - Identify site issues, ensure proper escalation, if necessary, and ensure resolution; create trip reports, confirmation/follow-up correspondence and telephone contacts for assigned sites; respond to audit findings; adhere to proper lines of communication within Celgene; attend and participate in study team meetings; keep information in the CTMS current; maintain calendar
  • Development - Maintain up-to-date medical and clinical knowledge for assigned therapeutic areas; mentor/coach new CRAs; maintain annual training records
  • Corporate Goals - Identify/evaluate potential investigators for future Celgene studies; build effective and positive relationships with Principal Investigators; ensure timely submission and review of CRF data and query resolution according to timelines set forth in the SMP; schedule travel following Celgene’s travel policy, and submit expense reports in an accurate and timely manner
  • Regulatory Documentation - Prepare ethics submissions and local regulatory documents at the country level, as needed; maintain local document files at a country level, as needed; review translations for ICD and other study documents, as needed; oversee to assure SOPs are followed in obtaining translations on necessary study documents
  • Monitoring Lead (As assigned) - Serve on study team as monitoring representative; review RFPs regarding monitoring specifications; develop the study monitoring plan and subsequent revisions; review, track and acknowledge monitoring visit reports; manage and track monitoring site visits to ensure quality monitoring; ensure adequate monitoring resources; ensure monitors are trained properly in the study requirements; track and report critical issues to study team; participate in CRF and protocol review process; attend, participate and present at Investigator Meetings; perform field assessments of Celgene and CRO FMs, as required; develop study-specific tools for Investigative sites and Field Monitors; conduct FM meetings; oversee CRO monitoring, as required
  • Significant medical and scientific knowledge
  • Significant knowledge of monitoring
  • Significant knowledge of medical terminology
  • Experience preparing for and presenting at investigator meetings
  • Ability to comprehend protocols and supportive information
  • Ability to work in a cross-functional team environment
  • Significant knowledge of Esystems (Inform, CTMS, etc)
  • Ability to travel extensively within Canada including overnight stays (approximately 50%)
  • Ability to drive an automobile and have a valid driver’s license
25

Senior Clinical Research Associate, Oncology Resume Examples & Samples

  • Manage specific study responsibilities as assigned by Sr. Manager or Clinical Operations Director/Sr. Director
  • Ensure Investigational Product (IP) needs for clinical studies are available and managed appropriately
  • The candidate must have a good working knowledge of medical terminology, physiology and pharmacology and an excellent knowledge of applicable U.S.; international regulations and guidelines, is preferred, but not required
  • Excellent oral and written communication, organizational and planning skills are required, ideally with the ability to manage budgets