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Clinical trials associate vs clinical research manager

The differences between clinical trials associates and clinical research managers can be seen in a few details. Each job has different responsibilities and duties. It typically takes 1-2 years to become both a clinical trials associate and a clinical research manager. Additionally, a clinical research manager has an average salary of $96,504, which is higher than the $74,952 average annual salary of a clinical trials associate.

The top three skills for a clinical trials associate include informed consent, patients and clinical operations. The most important skills for a clinical research manager are patients, oversight, and FDA.

Clinical trials associate vs clinical research manager overview

Clinical Trials AssociateClinical Research Manager
Yearly salary$74,952$96,504
Hourly rate$36.03$46.40
Growth rate6%6%
Number of jobs55,487100,000
Job satisfaction--
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 55%
Average age4444
Years of experience22

What does a clinical trials associate do?

A clinical trial associate is in charge of coordinating and executing clinical trial operations, ensuring to meet all goals within budgets and deadlines. Their responsibilities revolve around preparing and processing necessary documentation and certifications, submitting requirements to government agencies, distributing essential materials within the clinical teams, and reviewing study sheets, ensuring every paperwork is complete and accurate. Furthermore, as a clinical trial associate, it is vital to lead while implementing the company's policies and regulations, including its vision and mission.

What does a clinical research manager do?

A clinical research manager is responsible for leading a clinical research team in conducting clinical trials for medical purposes. Clinical research managers conduct scientific investigations, following critical methods and procedures within the budget goals and discussed timeframe. They monitor the adequacy of laboratory tools and equipment, request purchase orders, and ensure the authenticity of the materials for the accuracy of findings. A clinical research manager also enforces strict safety standards and protocols during clinical trials to avoid potential hazards and chemical contamination.

Clinical trials associate vs clinical research manager salary

Clinical trials associates and clinical research managers have different pay scales, as shown below.

Clinical Trials AssociateClinical Research Manager
Average salary$74,952$96,504
Salary rangeBetween $46,000 And $121,000Between $66,000 And $140,000
Highest paying CitySan Francisco, CASouth San Francisco, CA
Highest paying stateCaliforniaCalifornia
Best paying companyDorsey & WhitneyVarian Medical Systems
Best paying industryPharmaceuticalPharmaceutical

Differences between clinical trials associate and clinical research manager education

There are a few differences between a clinical trials associate and a clinical research manager in terms of educational background:

Clinical Trials AssociateClinical Research Manager
Most common degreeBachelor's Degree, 62%Bachelor's Degree, 55%
Most common majorBiologyNursing
Most common collegeUniversity of PennsylvaniaUniversity of Pennsylvania

Clinical trials associate vs clinical research manager demographics

Here are the differences between clinical trials associates' and clinical research managers' demographics:

Clinical Trials AssociateClinical Research Manager
Average age4444
Gender ratioMale, 25.3% Female, 74.7%Male, 21.5% Female, 78.5%
Race ratioBlack or African American, 2.5% Unknown, 7.4% Hispanic or Latino, 13.9% Asian, 13.4% White, 62.3% American Indian and Alaska Native, 0.5%Black or African American, 2.6% Unknown, 7.6% Hispanic or Latino, 15.0% Asian, 9.3% White, 65.1% American Indian and Alaska Native, 0.5%
LGBT Percentage9%9%

Differences between clinical trials associate and clinical research manager duties and responsibilities

Clinical trials associate example responsibilities.

  • Manage trial master files and study document to meet GCP/ICH and internal guidelines for records retention.
  • Audit TMF to ensure all require regulatory documentation are collected and lead.
  • Work closely with investigators to recruit eligible patients to clinical protocols, manage data collection and preparation.
  • Preform ICF customization in accordance with ICH guidelines, GCP s and local regulatory requirements.
  • Support the setup, data entry and QC of the system to ensure accuracy and quality of data.
  • Monitor clinical data and resolve inconsistencies according to FDA regulations and ICF guidelines.
  • Show more

Clinical research manager example responsibilities.

  • Launch and manage a regional CRA monitoring group that grow to 100 plus staff in two years.
  • Manage all planning and execution of oncology clinical trials, domestic and international, including decision impact and companion diagnostic trials.
  • Prepare applications to have studies approve by hospital's institutional review board (IRB) and help present study to IRB.
  • Develop an open access communication method for patients to discuss their questions and/or concerns with the principal investigators.
  • Major contributor to the NDA for both Depo-Provera contraceptive as well as Caverject for erectile dysfunction.
  • Interview, select, train, and monitor all clinical sites; negotiate site and CRO budgets.
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Clinical trials associate vs clinical research manager skills

Common clinical trials associate skills
  • Informed Consent, 9%
  • Patients, 7%
  • Clinical Operations, 6%
  • FDA, 6%
  • Consent Forms, 5%
  • TMF, 5%
Common clinical research manager skills
  • Patients, 9%
  • Oversight, 8%
  • FDA, 5%
  • IRB, 5%
  • Project Management, 5%
  • Data Management, 4%

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