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Become A Clinical Trials Associate

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Working As A Clinical Trials Associate

  • Getting Information
  • Establishing and Maintaining Interpersonal Relationships
  • Making Decisions and Solving Problems
  • Organizing, Planning, and Prioritizing Work
  • Updating and Using Relevant Knowledge
  • Mostly Sitting

  • $72,265

    Average Salary

What Does A Clinical Trials Associate Do At Kelly Services

* Responsible for clinical administrative operations activities involving clinical contract and budget support including but not limited to filing, scanning, mailing, populating spreadsheets and other administrative tasks as assigned.
* Duties and functions include:
* Create and maintain study specific file structures for TMF documentation and file documents accordingly.
* Create file folders/labels according to TMF plan, file incoming documents, retrieve documents, schedule document review.
* Ensure record filing is kept up to date and is performed accurately.
* Offsite archival of documents; ensure appropriate documentation completed to track archival.
* Conversion of paper documents to electronic records.
* Participate in continued security and maintenance of the Trial Master File (TMF) Room.
* Completes responsibilities in a timely, organized way.
* Identifies issues/problems and provides customary recommendations for solutions.
* Demonstrates excellent verbal, written, and interpersonal communication skills.
* Performs routine work without detailed instructions.
* Interacts well with teams.
* Supports senior peers on non-complex projects to learn through experience

What Does A Clinical Trials Associate Do At Vanderbilt University Medical Center

* Coordinate protocol and patient consent form process.
* Coordinates preparation of all IRB and regulatory documents; under direction of PI may draft various communications with Sponsor.
* Develops assessment tool pre protocol to use in clinical research.
* May assist PI in obtaining Informed Consent from study participant and documents appropriately.
* Identifies and recruits clinical research subjects; monitors enrollment goals and modifies recruitment strategies, as necessary.
* Processes patient data and runs reports as needed.
* Processes and ships lab specimens efficiently and cost effectively; maintains supply inventory and equipment; maintains regulatory standards.
* Develops procedures for lab collection and storage.
* May provide annual reporting to IRB and prepare annual summaries.
* Abstracts and records all patient data essential to the study onto required case report forms or into the electronic data collection system.
* Sets up timeline of tests and required procedures for nurse.
* Inputs all pertinent patient data into database accurately.
* Collects and monitors all study patient records to document treatments and outcomes as required by the protocol.
* Report all adverse reactions according to VU and protocol guidelines.
* Check values from lab and rates toxicity levels.
* May coordinate with research investigators, monitors, IRB and sponsors regarding approval process with IRB.
* Process Improvement
* Institutes process improvement measures for efficiency and productivity within the dept.
* Initiates and develops new procedures to improve quality and efficiency in the dept.
* Trains and mentors new staff to perform job duties at an acceptable level and understand new processes and regulations.
* Encourages new employees to ask questions to spur process improvement.
* Pursues professional development and participate on committees, as requested by management.
* Associate's Degree (or equivalent experience) and 2 years experience

What Does A Clinical Trials Associate Do At University of IOWA

* The "Paleolithic Feeding Study (PFS)" aims to improve our understanding of the impact of diet on fatigue in patients with Multiple Sclerosis.
* The College of Nursing Paleo Feeding Study seeks to recruit a Study Coordinator/Data Manager to join their team responsible to:Assist in the design, development, execution, and maintenance of protocols for this clinical study.
* This includes maintaining and updating as needed the Manual of Procedures and Human Subjects/IRB compliance and Clinical Trial Registration (ClinicalTrial.gov).
* The Coordinator will (a) complete required forms (letters of agreement, HIPPA form, Individual Investigator Agreements); (b) facilitate completion of human subjects training (CITI) and certification by designated staff; (c) submit IRB modifications, as needed; (d) facilitate project staff training, as needed; and (e) manage and maintain the ongoing updating process necessary for proper Clinical Trial Registration
* Serve as the primary contact person for participants and project staff/faculty.
* Assist, facilitate and monitor activities, including but not limited to (a) recruiting, screening, and enrolling participants (including informed consent); (b) coordinating with the metabolic kitchen to provide the dietary intervention; c) assisting with data collection; and (d) scheduling appointments and telephone interviews with UI study team members
* Manage project data.
* Collaborate with the Investigators and RAs to assure the data entry system (REDCap) accurately reflects the data collection process, the data dictionary is fully functional, and data transfer to analytic software is seamless.
* Responsible for merging and cleaning data, and creating a useable data structure.
* Assist in judging the validity of data and make recommendations.
* Other duties may include: 1) modifying and/or writing program code to create forms and reports that meet project staff needs; 2) working with PI and statistician to analyze data, prepare reports, and develop graphs; 3) supporting data access and administration; and 4) providing operational support for database backup and recovery
* Implement/oversee study participant payments
* Oversee financial resources, including but not limited to (a) ordering/acquiring study-related equipment and materials; (b) monitoring study expenditures; (c) reconciling Electronic Transaction Detail Reports (TDR); and (d) collaborating with investigators to produce reports to funding agencies and others
* Assist Senior/Key Personnel to summarize and synthesize study findings for purposes of generating study-related funding reports, papers, and other scholarly dissemination activities
* The hired candidate will need to successfully complete training and certification for clinical trial research within the first month of employment
* References: Five professional references will be requested and required at a later step in the recruitment process
* This requisition is intended to hire one individual for a specified term position funded for one year.
* Funding beyond beyond one year may be available, however is uncertain at this time
* The salary range for this position has a minimum starting salary of $30,603/yr for 75% appointment or $40,805/yr minimum starting salary for a 100% (fulltime) appointment.
* Salary will be determined based on the transferable experience level of the selected candidate and the negotiated percent of appointment

What Does A Clinical Trials Associate Do At System One Services

Assist with documents during study start-up including CDAs and CTAs

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How To Become A Clinical Trials Associate

Natural sciences managers usually advance to management positions after years of employment as scientists. Natural sciences managers typically have a bachelor’s degree, master’s degree, or Ph.D. in a scientific discipline or a related field, such as engineering. Some managers may find it helpful to have an advanced management degree—for example, a Professional Science Master’s (PSM) degree, a Master of Business Administration (MBA), or a Master of Public Administration (MPA).

Education

Natural sciences managers typically begin their careers as scientists; therefore, most have a bachelor’s degree, master’s degree, or Ph.D. in a scientific discipline or a closely related field, such as engineering. Scientific and technical knowledge is essential for managers because they must be able to understand the work of their subordinates and provide technical assistance when needed. 

Natural sciences managers who are interested in acquiring postsecondary education in management should be able to find master’s degree or Ph.D. programs in a natural science that incorporate business management courses. A relatively new type of degree, called the Professional Science Master’s (PSM), blends advanced training in a particular science field with business skills, such as communications and program management, and policy. Those interested in acquiring general management skills may pursue a Master of Business Administration (MBA) or a Master of Public Administration (MPA). Some natural sciences managers will have studied psychology or some other management-related field to enter this occupation.

Sciences managers must continually upgrade their knowledge because of the rapid growth of scientific developments.

Work Experience in a Related Occupation

Natural sciences managers usually advance to management positions after years of employment as scientists. While employed as scientists, they typically are given more responsibility and independence in their work as they gain experience. Eventually, they may lead research teams and have control over the direction and content of projects before being promoted to an administrative position.

Licenses, Certifications, and Registrations

Although certification is not typically required to become a natural sciences manager, many relevant certifications are available. These certifications range from those related to specific scientific areas of study or practice, such as laboratory animal management, to general management topics, such as project management, and are useful to natural sciences managers regardless of the organization being managed.

Important Qualities

Communication skills. Natural sciences managers must be able to communicate clearly to a variety of audiences, such as scientists, policymakers, and the public. Both written and oral communication are important.

Critical-thinking skills. Natural sciences managers must carefully evaluate the work of others. They must determine if their staff’s methods and results are based on sound science.

Interpersonal skills. Natural sciences managers lead research teams and therefore need to work well with others in order to reach common goals. Managers routinely deal with conflict, which they must be able to turn into positive outcomes for their organization.

Leadership skills. Natural sciences managers must be able to organize, direct, and motivate others. They need to identify the strengths and weaknesses of their workers and create an environment in which the workers can succeed.

Problem-solving skills. Natural sciences managers use scientific observation and analysis to find solutions to complex technical questions.

Time-management skills. Natural sciences managers must be able to do multiple administrative, supervisory, and technical tasks while ensuring that projects remain on schedule.

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Clinical Trials Associate jobs

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Clinical Trials Associate Demographics

Gender

  • Female

    71.5%
  • Male

    25.7%
  • Unknown

    2.7%

Ethnicity

  • White

    76.7%
  • Asian

    10.7%
  • Hispanic or Latino

    9.2%
  • Unknown

    2.3%
  • Black or African American

    1.0%
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Languages Spoken

  • Spanish

    29.0%
  • French

    9.7%
  • Arabic

    9.7%
  • Mandarin

    6.5%
  • Hindi

    6.5%
  • Swedish

    3.2%
  • Chinese

    3.2%
  • Vietnamese

    3.2%
  • Greek

    3.2%
  • Turkish

    3.2%
  • Japanese

    3.2%
  • Amharic

    3.2%
  • Urdu

    3.2%
  • Polish

    3.2%
  • Cantonese

    3.2%
  • Gujarati

    3.2%
  • Armenian

    3.2%
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Clinical Trials Associate

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Clinical Trials Associate Education

Clinical Trials Associate

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Real Clinical Trials Associate Salaries

Job Title Company Location Start Date Salary
Senior Clinical Trial Mangement Associate Populus Group LLC Foster City, CA Jun 09, 2016 $127,307
Senior Clinical Trial Management Associate-HIV Gilead Sciences, Inc. Foster City, CA Nov 19, 2015 $119,038
Clinical Trial Associate Novartis Institutes for Biomedical Research, Inc. Cambridge, MA Sep 18, 2016 $97,577
Associate Clinical Trial Leader Novartis Pharmaceuticals Corporation Florham Park, NJ Oct 01, 2014 $96,189
Associate Clinical Trial Leader Novartis Pharmaceuticals Corporation Florham Park, NJ Mar 19, 2012 $93,000
Associate Clinical Trial Leader Novartis Pharmaceuticals Corporation East Hanover, NJ Aug 06, 2014 $90,000
Senior Clinical Trial Disclosure Associate Abbvie Inc. North Chicago, IL Nov 04, 2016 $85,000 -
$91,000
Clinical Trial Associate Smith Hanley Consulting Group, LLC South San Francisco, CA Nov 19, 2012 $83,480
Clinical Trials Associate Solta Medical, Inc. Hayward, CA May 03, 2010 $80,000
Clinical Trial Associate Acorda Therapeutics, Inc. Ardsley, NY Jun 27, 2016 $75,000
Senior Clinical Trial Management Associate-Hiv Gilead Sciences, Inc. Foster City, CA Mar 25, 2013 $72,530 -
$91,727
Clinical Trial Disclosure Associate Abbvie Inc. North Chicago, IL Jul 25, 2014 $72,000
Senior Clinical Trial Management Associate Gilead Sciences, Inc. Foster City, CA Jul 12, 2015 $71,822 -
$105,084
Clinical Trial Associate Precept Technology, L.C. Jersey City, NJ Aug 27, 2012 $66,560
Clinical Trial Associate Alkermes, Inc. Waltham, MA Apr 20, 2015 $65,000 -
$70,000
Associate, Clinical Trial Management Inventiv Health Clinical SRS, LLC Columbus, IN Dec 02, 2013 $65,000
Senior Clinical Trial Management Associate, HBV Gilead Sciences, Inc. Foster City, CA Apr 04, 2013 $53,310 -
$110,946
Clinical Trial Documents Associate Ophthalmic Research Associates, Inc. Andover, MA Sep 16, 2014 $45,000
Clinical Trial Associate TKL Research Inc. Rochelle Park, NJ May 29, 2012 $44,871

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Top Skills for A Clinical Trials Associate

RegulatoryDocumentsStudyProtocolIRBFDACROTMFCrasStudyDocumentsSafetyReportsProceduresCRFInvestigatorMeetingsInvestigativeSitesStudySitesCtmsMeetingMinutesDataEntryStudyStart-UpAuditOncology

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Top Clinical Trials Associate Skills

  1. Regulatory Documents
  2. Study Protocol
  3. IRB
You can check out examples of real life uses of top skills on resumes here:
  • Reviewed regulatory documents from participating clinical trial sites.
  • Assisted with Document Management activities, including editing study protocols and amendments.
  • Communicate and support field monitors, IRBs and outside vendors as to study issues and updates.
  • Maintain regulatory documents for FDA and research sponsor
  • Lead team of 10+ Clinical Trials Associates (CTAs) supporting studies across multiple therapeutic areas.

Top Clinical Trials Associate Employers

Clinical Trials Associate Videos

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Clinical Research Associates & Project Managers

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