Skip to main content

Sr CRA, Oncology, Cell and Gene Therapy, Central - IQVIA Biotech

Location: Wilmington, North Carolina; Coeur d'Alene, Idaho; Colby, Kansas; Columbia, Missouri; Corpus Christi, Texas; Fargo, North Dakota; Flagstaff, Arizona; Flint, Michigan; Fort Wayne, Indiana; Fort Worth, Texas; Huntley, Illinois; Hutchinson, Kansas; Idaho Falls, Idaho; Independence, Iowa; Iowa City, Iowa; Lawrenceville, Illinois; Lenexa, Kansas; Liberty, Missouri; Manhattan, Kansas; McAllen, Texas; McHenry, Illinois; Memphis, Tennessee; Newark, Ohio; Norman, Oklahoma; Novato, California; Oak Park, Illinois; Ogden, Utah; Oklahoma City, Oklahoma; Olathe, Kansas; Omaha, Nebraska; Quincy, Illinois; Racine, Wisconsin; Rhinelander, Wisconsin; Richmond, Indiana; Scottsbluff, Nebraska; Sikeston, Missouri; Sioux City, Iowa; Sioux Falls, South Dakota; Skokie, Illinois; Southfield, Michigan; Terre Haute, Indiana; Texarkana, Texas; Tinley Park, Illinois; Topeka, Kansas; Traverse City, Michigan; Wichita, Kansas
R1215456

At IQVIA Biotech, we’re bringing something new to the industry. A flexible model, therapeutically-aligned teams and dedicated resources in a transparent partnership. As a Senior Clinical Research Associate, you’ll have the opportunity to work directly with customers in a collaborative environment where you'll help change the face of biotech.

In this highly specialized and dynamic role, you’ll utilize your extensive therapeutic knowledge to oversee uniquely-focused clinical studies. Working at the core of clinical research, you’ll be exposed to cutting-edge protocols and experience a dedicated partnership with your team like never before.

Join us and help reimagine the future of biotech.

  • Full Time
  • Level: Senior
  • Travel: Yes

Success profile

What makes a Senior Clinical Research Associate at IQVIA Biotech successful? Check out the top traits we’re looking for and see if you have the right mix.

  • COLLABORATIVE
  • INDEPENDENT
  • DETAIL-ORIENTED
  • ORGANIZED
  • EFFICIENT
  • PROBLEM-SOLVER

Explore this
career path

As you grow your CRA career at IQVIA Biotech, you’ll play an important role in helping our customers drive healthcare forward and impact the lives of patients around the world.

Quote

Leah

What makes IQVIA Biotech different from my past companies is that I partner directly with smaller pharmaceutical companies and am able to become a true ‘expert’ by being aligned with a smaller amount of projects with a larger site load. IQVIA Biotech promotes a strong culture of communication and mentorship and I’ve thoroughly enjoyed my time since joining last year.

Leah, Clinical Research Associate 2
Nikesh

I’ve had the opportunity to work on several different studies from medical device to oncology and from study start up to site close out, each of which have been great experiences. Last year, I was promoted to CRA 2 after developing my knowledge and skills through the numerous site visits I completed. I really do feel appreciated for the work I do. It feels great to be a part of IQVIA Biotech where we can contribute our ideas and knowledge and be supported by our management team and colleagues!

Nikesh, Clinical Research Associate 2

What you
can expect

  • Professional Development

    Resources that promote your career growth

  • Work-Life Balance

    Leaders that support flexible work schedules

  • Highly Specialized

    Roles that require specialty knowledge and training

  • Therapeutically Aligned

    Protocols aligned to your specific expertise

  • Variety

    Dynamic work environments that expose you to new experiences

  • Best-in-class Training

    Programs to help you build your therapeutic-knowledge

Sr CRA, Oncology, Cell and Gene Therapy, Central - IQVIA Biotech

Apply now
Location: Abilene, Texas, United States, USA; Ada, Oklahoma, United States, USA; Adair, Iowa, United States, USA; Bismark, North Dakota, United States, USA; Bloomington, Indiana, United States, USA; Breckenridge, Colorado, United States, USA; Coeur d'Alene, ID, USA; Colby, KS, USA; Columbia, MO, USA; Corpus Christi, TX, USA; Evanston, Wyoming, United States, USA; Fargo, ND, USA; Flagstaff, AZ, USA; Flint, MI, USA; Fort Wayne, IN, USA; Fort Worth, TX, USA; Huntley, IL, USA; Hutchinson, KS, USA; Idaho Falls, ID, USA; Independence, IA, USA; Iowa City, IA, USA; Lawrenceville, IL, USA; Lenexa, KS, USA; Liberty, MO, USA; Manhattan, KS, USA; McAllen, TX, USA; McHenry, IL, USA; Memphis, TN, USA; Mount Vernon, Illinois, United States, USA; Newark, OH, USA; Norman, OK, USA; Novato, CA, USA; Oak Park, IL, USA; Ogden, UT, USA; Oklahoma City, OK, USA; Olathe, KS, USA; Omaha, NE, USA; Quincy, IL, USA; Racine, WI, USA; Rhinelander, WI, USA; Richmond, IN, USA; Santa Fe, New Mexico, United States, USA; Scottsbluff, NE, USA; Shenandoah, Texas, United States, USA; Sikeston, MO, USA; Sioux City, IA, USA; Sioux Falls, SD, USA; Skokie, IL, USA; Somerset, Kentucky, United States, USA; Somerville, Tennessee, United States, USA; South Shore, Illinois, United States, USA; Southbend, Indiana, United States, USA; Southfield, MI, USA; Terre Haute, IN, USA; Texarkana, TX, USA; Tinley Park, IL, USA; Topeka, KS, USA; Traverse City, MI, USA; Wichita, KS, USA R1215456

Job description

POSITION TITLE:                     Senior Clinical Research Associate (CRA)

REPORTS TO:                             Director/Associate Director, Clinical Monitoring (US) or Designee

                                                            CRA Manager (EU) or Designee

BASIC FUNCTIONS:

Participates in the preparation and execution of Phase I-IV clinical trials. Oversees the progress of clinical investigations by conducting site evaluation, initiation, and interim close out visits to sites.  Monitors clinical trials in accordance with Good Clinical Practices and procedures set forth by IQVIA Biotech and sponsors. Works closely with the Clinical Trial Manager (CTM) and/or Lead CRA t0 ensure all monitoring activities are conducted according to study requirements. The Senior CRA may also serve in the Lead CRA role.

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

  • Participates in the investigator recruitment process. Performs site evaluation visits of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
  • Collaborates with the ISS department to coordinate activities with the site in preparation for the initiation of the study. Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISS and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
  • Performs study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
  • Trains site staff on the EDC system and verifies site computer system.
  • Assists in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
  • Assures 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 IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
  • Documents 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.
  • Reviews the quality and integrity of the clinical data through (1) in house review of electronic CRF data and (2) on-site source verification. Works with sites to resolve data queries.
  • May review protocols, eCRFs, study manuals and other related documents, as requested by the Clinical Trial Manager and/or Lead CRA.
  • Serves as primary contact between IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
  • Performs study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
  • Assists with, and attends, Investigator Meetings for assigned studies.
  • Authorized to request site audits due to data integrity concerns.
  • Attends study-related, company, departmental, and external meetings, as required.
  • Ensures internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
  • Ensures all study deliverables are completed per IQVIA Biotech and study timelines
  • Conducts Field Evaluation Visits and field training of CRA Is, IIs and other Sr. CRAs.
  • Serves as mentor for junior CRAs and those new to the company and/or study.
  • Performs other duties, as requested.

LEAD CRA ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

The Lead Clinical Research Associate mayperform any of the following tasks:

  • Participate in the investigator recruitment process. Perform site evaluation visits, as needed, of potential investigators. Evaluates the capability of the site to successfully manage and conduct the clinical study.
  • Collaborate with the ISS department to coordinate activities with the site in preparation for the initiation of the study.  Obtains regulatory documentation for successful implementation, monitoring, and evaluation of clinical trials. Works with ISS and site staff to obtain regulatory (IRB/IEC) approval of study specific documents
  • Perform study initiation activities, reviewing with the site personnel the protocol, regulatory issues, study procedures, and provides training on completion of the eCRF; monitoring activities and study close-out activities.
  • Assists with, and attends, Investigator Meetings for assigned studies.
  • Train site staff on the EDC system and verify site computer system.
  • Assist in resolving any issues to ensure compliance with site file audits in conjunction with ISS.
  • 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 IQVIA Biotech SOPs by using approved IQVIA Biotech/sponsor templates and reports.
  • 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.
  • 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 IQVIA Biotech and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
  • Assist CTM and/or PM in review of project budgets, monitoring costs, potential overruns and propose/implement cost effective solutions.
  • Assist the study management in identifying and generating changes in scope
  • Perform study close-out visits per the study specific Clinical Monitoring Plan including final investigational product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
  • Authorized to request site audits due to data integrity concerns.
  • Attends study-related, company, departmental, and external meetings, as required.
  • Ensure internal and study-related trainings are completed per IQVIA Biotech and/or study timelines; CTMS should always be current with the pertinent site updates/contacts.
  • Ensure all study deliverables are completed per IQVIA Biotech and study timelines
  • May conduct Field Evaluation Visits and field training of CRA Is, IIs and Sr CRAs.
  • Serve as mentor for junior CRAs and those new to the company and/or study.
  • Participate in the performance appraisal program by providing timely and accurate feedback regarding the performance of a perspective CRA.
  • Review and approve CRA travel expenses and time sheets.
  • Perform other duties, as requested.

TECHNICAL CTM ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

The Technical CTM may perform any of the following tasks for oncology studies:

  • Create master tracker(s) to house information generated from various reports such as:
  • and CM_Data_Cleaning_Report_By_Subject both Business Objects reports 
  • Reconcile patients that have come off treatment and off study
  • Generate and review various IL2 reports
  • Works closely with CDRC to ensure data is further reviewed and discrepancies documented.
  • The Technical CTM may participate in CDRC review and aid in Patient Profile review, as necessary.
  • There may be additional tracking required as a result of CDRC’s review.

KNOWLEDGE, SKILLS AND ABILITIES:

  • Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and medical terminology.
  • Four+ years of oncology experience and/or medical device.
  • Experience in monitoring and/or coordinating clinical trials required.
  • Excellent written and verbal communication skills to express complex ideas to study personnel at research and clinical institutions.
  • Demonstrated ability to form strong functional relationships.
  • Excellent, presentation, organizational and interpersonal skills.
  • Ability to interact with all levels of staff to coordinate/execute study activities.
  • Ability to handle several priorities within multiple, complex trials.
  • Ability to reason independently and recommend specific solutions in clinical settings.
  • Ability to work independently, prioritize, and work within a matrix team environment.
  • Ability to mentor other CRAs and co-monitor, as required.
  • Knowledge of electronic data capture including basic data processing functions.
  • Knowledge of current GCP/ICH guidelines applicable to the conduct of clinical research.
  • Able to qualify for a major credit card, rent an automobile
  • For the Technical CTM role, the CRA must have a deep understanding of IQVIA Biotech systems with the ability to learn even more.

PHYSICAL REQUIREMENTS:

  • Very limited physical effort required to perform normal job duties
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech
  • Extensive use of keyboard requiring repetitive motion of fingers
  • Regular sitting for extended periods of time

MINIMUM RECRUITMENT STANDARDS:

  • BS/BA/BSc (or equivalent) in one of the life sciences or health care background (RPh, RN, etc) and a minimum of four (4) years of monitoring/site management experience is required; or equivalent combination of education, training and experience.
  • Prior Clinical Research Organization (CRO) experience preferred.
  • Prior project team leadership experience preferred.
  • Working knowledge of budget management preferred.
  • Must be able to travel domestically and internationally approximately 65%-85%.
  • Valid driver’s license
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer

CLASSIFICATION (US):

This position is classified as exempt under the Fair Labor Standards Act; employees are not eligible for overtime compensation.

#remote

#CRAIBAJD

#LI-SA3

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA, Inc. provides reasonable accommodations for applicants with disabilities.  Applicants who require reasonable accommodation to submit an application for employment or otherwise participate in the application process should contact IQVIA’s Talent Acquisition team at workday_recruiting@iqvia.com to arrange for such an accommodation.

In compliance with the Colorado Equal Pay For Equal Work Act, salary range is displayed - Salary Pay Range: $100,000 - $125,000

Apply now
Smiling girl

Join IQVIA’s Talent Network

Let’s stay connected. Join our global Talent Network to receive alerts when new opportunities become available that match your career ambitions.

Join our network
Top of page