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Temporary Clinical Trial Data Entry Jobs in Indiana

Lilly

Clinical Data Associate

Indianapolis, IN

The Clinical Data Associate is required to represent the clinical data sciences function and ... Partner with across functional team members to ensure trial success through robust oversight/review ...

Actalent

Clinical Pharmacist

Indianapolis, IN · On-site

$113.30K - $135.30K/yr

Act as a liaison between the data entry area and production to maintain smooth operations and ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Actalent

Clinical Pharmacist

Indianapolis, IN

$103.90K - $124.10K/yr

Act as a liaison between the data entry area and production to maintain smooth operations and ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Actalent

Clinical Pharmacist

Indianapolis, IN

$103.90K - $124.10K/yr

Act as a liaison between the data entry area and production to maintain smooth operations and ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

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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.

What are the most commonly searched types of Clinical Trial Data Entry jobs in Indiana? The most popular types of Clinical Trial Data Entry jobs in Indiana are:
What are popular job titles related to Temporary Clinical Trial Data Entry jobs in Indiana? For Temporary Clinical Trial Data Entry jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Temporary Clinical Trial Data Entry jobs in Indiana look for? The top searched job categories for Temporary Clinical Trial Data Entry jobs in Indiana are:
What cities in Indiana are hiring for Temporary Clinical Trial Data Entry jobs? Cities in Indiana with the most Temporary Clinical Trial Data Entry job openings:
Temporary Clinical Trial Data Entry jobs near you
Site Manager (Clinical Trials Facility)

Site Manager (Clinical Trials Facility)

Protouch Staffing

Merrillville, IN • On-site

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 8 days ago

Job description

Clinical Research Site Manager

(Lead CRC or Senior CRC with Management Experience)

Location: Merrillville, IN

Job Type: Full-Time

Schedule: Monday-Friday (5x8 shifts)

Salary Range: $95K to $110K + Profit Distribution


Position Summary

The Clinical Research Site Manager is responsible for overseeing the daily operations of the clinical research site, ensuring strict protocol compliance, high-quality patient care, and seamless coordination with sponsors and CROs. This role leads site staff, monitors study performance, and ensures adherence to regulatory and ethical standards.


Key Responsibilities

  • Oversee daily site operations and ensure compliance with GCP, FDA, and ICH guidelines

  • Supervise and support Clinical Research Coordinators (CRCs), nurses, and clinical staff

  • Serve as the primary point of contact for sponsors, CROs, and monitors

  • Oversee patient recruitment, informed consent, and retention strategies

  • Ensure accurate data entry and timely resolution of data queries

  • Manage study budgets, contracts, and allocation of site resources

  • Maintain regulatory documentation and audit readiness


Qualifications

  • Bachelor's degree in Life Sciences, Nursing, or related field (Master's preferred)

  • 3-5 years of clinical research experience

  • 1-2 years of leadership or site management experience

  • Strong working knowledge of GCP, FDA, and ICH regulations

  • Excellent leadership, communication, and organizational skills


Benefits

  • Health, Dental, and Vision Insurance

  • Paid Time Off (PTO)

  • Retirement Plan

  • Profit Distribution

Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989

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