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Temporary Clinical Trial Data Entry Jobs in Indiana

Medix

Oncology Nurse (Clinical Research)

Indianapolis, IN · On-site

$24.83 - $46.12/hr

Prior experience with electronic medical records (EMR), clinical trial data entry systems (EDC), and Clinical Trial Management Systems (CTMS) is preferred. Schedule/Shift Monday - Friday 8:00 am - 5 ...

Alignerr

Medical Science Liaison (MSL)

Indianapolis, IN · Remote

Validate that complex clinical trial data, safety information, and medical evidence are accurately represented in AI outputs * Develop and assess scientific communication strategies grounded in real ...

Lilly

Data Scientist

Indianapolis, IN · On-site

You'll analyze complex datasets - regulatory documents, clinical trial data, submission timelines, operational metrics - to uncover patterns, build predictive models, and develop AI-powered solutions.

Veteran's Institute of Wellness (VIWEll)

Be Seen First

Clinical Research Specialist

Indianapolis, IN · On-site

$16.50 - $24.50/hr

We are driven by a profound goal: we are conducting a clinical trial to repurpose low-cost ... Data extraction from an electronic medical record. * Data entry into databases and Excel ...

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Temporary Clinical Trial Data Entry information

What are the key skills and qualifications needed to thrive as a Temporary Clinical Trial Data Entry specialist, and why are they important?

To thrive as a Temporary Clinical Trial Data Entry specialist, you need strong attention to detail, organizational skills, and familiarity with data management, typically supported by a high school diploma or higher. Proficiency in electronic data capture (EDC) systems, Microsoft Excel, and sometimes Good Clinical Practice (GCP) certification is valuable. Excellent time management, accuracy under pressure, and effective communication are standout soft skills for this position. These skills ensure the integrity, reliability, and timely processing of clinical trial data, which are critical for successful research outcomes.

What are some common challenges faced in a Temporary Clinical Trial Data Entry role, and how can they be managed?

One of the main challenges in a Temporary Clinical Trial Data Entry position is maintaining high accuracy and attention to detail while working with large volumes of sensitive data under tight deadlines. It's important to stay organized and follow established protocols to minimize errors and ensure compliance with regulatory standards. Collaborating closely with clinical research coordinators and data managers can help clarify uncertainties and maintain data integrity. Regular communication and seeking feedback from the team are also valuable in overcoming these challenges.

What are Temporary Clinical Trial Data Entry jobs?

Temporary Clinical Trial Data Entry jobs involve entering, updating, and managing data collected during clinical trials on a short-term or contract basis. These professionals ensure that clinical data is accurately recorded in databases, following strict protocols to maintain data integrity and confidentiality. Tasks may include verifying patient information, inputting test results, and assisting with data audits. Temporary roles are often available during particularly busy phases of a clinical study or to cover for permanent staff absences.

What is the difference between Temporary Clinical Trial Data Entry vs Clinical Data Coordinator?

AspectTemporary Clinical Trial Data EntryClinical Data Coordinator
CredentialsHigh school diploma or equivalent; data entry experienceBachelor's degree in life sciences or related field; experience in data management
Work EnvironmentTemporary assignments in clinical research settings, often part-time or contractFull-time role in clinical research teams, overseeing data quality
Employer & Industry UsagePharmaceutical companies, CROs, research institutionsPharmaceutical companies, CROs, biotech firms

Temporary Clinical Trial Data Entry focuses on inputting data accurately during clinical trials, often on short-term contracts. Clinical Data Coordinators have broader responsibilities, including data validation, management, and ensuring compliance. While both roles require attention to detail, the coordinator role typically demands more experience and a higher level of responsibility.

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Temporary Clinical Trial Data Entry jobs near you
Clinical Data Associate

Clinical Data Associate

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 70 rated pharmaceutical

Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
The eDC Clinical Study Build Programmer is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth understanding of data technology, data flow, data standards, database programming, normalization and testing.
This role will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key partners to deliver standardized data collection methods and innovative validation solutions for use in global clinical trials.
Responsibilities:
Portfolio Delivery:
  • Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
  • Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
  • Provide insights into study level deliverables (i.e. Data Management Plan, Project Plan, database, and observed datasets)
  • Support submission, inspection and regulatory response activities
  • Lead cross Business Unit/Therapeutic Area projects or programs with high complexity
  • Opportunity to develop and tests new ideas and/or applies innovative solutions that add new value to the portfolio

Project Management:
  • Increase speed, accuracy, and consistency in the development of systems solutions
  • Enable metrics reporting of study development timelines and pre and postproduction changes to database
  • Partner to deliver study database per business need and before first patient visit
  • Follow and influence data standard decisions and strategies for a study and/or program
  • Apply therapeutic knowledge and possess a deep understanding of the technology used to collect clinical trial data
  • Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study build deliverables
  • Integrates multi-functional and/or external information and applies technical knowledge to data-driven decision making

Enterprise Leadership:
  • Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis
  • Represent Data and Analytics processes in multi-functional initiatives
  • Actively engage in shared learning across the organization
  • Work to Increase re-usability of forms and edits by improving the initial design
  • Work to reduce postproduction changes change control process
  • Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization
  • Interacts with regulators, business partners and outside stakeholders on business issues
  • Thinks with end to end in mind consistently managing risk to minimize impact on delivery
  • Builds a diverse multi-functional and internal/external network to understand how different disciplines and approaches contribute to research and development
  • Focuses on defining database solutions and timelines in support of advancing the portfolio

Other responsibilities
  • The experienced Clinical Study Build Programmer - eDC is expected to provide coaching and guidance for junior Clinical Study Build Programmers.
  • The Clinical Study Build Programmer - eDC may or may not lead a team of junior Clinical Study Build Programmers. If in supervisory positions, the Clinical Study Build Programmer - eDC is expected to:
  • Participate in the recruitment, development, and retention of a scientific, technical, and operationally capable workforce that is skilled and knowledgeable in end-to-end global clinical eDC system builds
  • Provide effective technical leadership to an agile team of technical staff that continuously meets the needs of a changing portfolio and demonstrates judgment-based decision making, and provide leadership in clinical eDC system build delivery
  • Creating a team culture that fosters inclusion and innovation and values diversity
  • Responsible for effective resource planning
  • Responsible for supervising clinical study build programmer staff, as assigned, including aspects of training, mentoring, goal setting, performance management, and engagement. Other activities include setting objectives, soliciting feedback from stakeholders, and conducting performance reviews to foster growth of staff.
  • Ensure all necessary training is provided to staff to support job performance and knowledge. Help to remove any barriers or obstacles that impede them from achieving company, functional, and individual objectives.

Basic Qualifications:
  • Master's degree in a scientific or technical field such as Informatics/Analytics, Life Sciences, Information Technology, Computer Sciences (or bachelor's degree plus 3 or more years of experience in clinical data management, database programming or system validation experience in the clinical, pharmaceutical, biotech, CRO or regulatory agency sectors)
  • Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position

Additional Preferences:
  • Knowledge of regulatory guidelines such as GCP, 21 CFR Part 11 etc.
  • Knowledge of industry standard clinical technologies including CTMS, EDC (Veeva CDMS preferred, Rave, InForm), eCOA, IxRS, Clinical Data Repositories, etc.
  • Knowledge of CDISC and CDASH standards/standard terminology
  • The ability to work independently as well as in a team environment.
  • Project and Vendor management experience
  • Excellent time management skills and a proven ability to work on multiple projects at any given time in a fast-paced environment.
  • Demonstrated ability to stay abreast of trends and new information in the profession.
  • Quick learner to new trends in technology
  • Excellent leadership, communication (written and oral) and interpersonal skills
  • Demonstrated teamwork and collaboration in a professional setting

Experience with the following:
  • Articulating the flow of data (structure and format) from patient to analysis and apply this knowledge to data solutions
  • Deciding the technology platform (system/database) for data acquisition and aggregation
  • Utilization of clinical/drug development knowledge and an ability to liaise effectively with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical)
  • Strong therapeutic/scientific knowledge in the field of research
  • Society of Clinical Data Management certification
  • Project management experience
  • Familiarity with clinical data tools and technologies
  • Understanding and experience in using data standards
  • Ability to balance multiple activities, prioritize and manage ambiguity
  • Demonstrated exemplary teamwork/interpersonal skills
  • Proven problem solving, attention to detail and result oriented behaviors in a fast-paced environment.

Other Information:
  • Domestic and International travel may be required

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $148,500
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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