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Tandem Clinical Research Jobs (NOW HIRING)

DM Clinical Research

Administrative Assistant

Philadelphia, PA · On-site

$18.25 - $24.50/hr

Administrative Assistant The Administrative Assistant works in tandem with our clinical research staff and multiple other departments to provide excellent customer care to patients participating in ...

DM Clinical Research

Administrative Assistant

Jersey City, NJ · On-site

$18.75 - $25.25/hr

Administrative Assistant The Administrative Assistant works in tandem with our clinical research staff and multiple other departments to provide excellent customer care to patients participating in ...

DM Clinical Research

Administrative Assistant

Phoenix, AZ · On-site

$17.75 - $24/hr

Administrative Assistant The Administrative Assistant works in tandem with our clinical research staff and multiple other departments to provide excellent customer care to patients participating in ...

DM Clinical Research

Administrative Assistant

Houston, TX

$17.25 - $23.25/hr

Administrative Assistant The Administrative Assistant works in tandem with our clinical research staff and multiple other departments to provide excellent customer care to patients participating in ...

DM Clinical Research

Medical Receptionist

Jersey City, NJ

$17.25 - $21/hr

Medical Receptionist The Medical Receptionist works in tandem with our clinical research staff and multiple other departments to provide excellent customer care to patients participating in our ...

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Tandem Clinical Research information

See salary details

$49K

$107.3K

$189K

How much do tandem clinical research jobs pay per year?

As of Sep 5, 2026, the average yearly pay for tandem clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is Tandem Clinical Research?

Tandem Clinical Research is an organization that conducts clinical trials to help develop new medical treatments and therapies. They partner with pharmaceutical companies, biotechnology firms, and medical device manufacturers to test the safety and effectiveness of drugs and interventions. Their team includes medical professionals who work with volunteers participating in these studies, ensuring ethical standards and regulatory compliance are met. Participating in their trials can help advance medical science and potentially provide access to new treatments.

What are the key skills and qualifications needed to thrive in clinical research roles at Tandem Clinical Research?

To thrive in a clinical research role at Tandem Clinical Research, you need a solid background in life sciences, clinical trial protocols, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and regulatory submission platforms is typically required. Strong attention to detail, organizational skills, and effective communication help ensure accurate data collection and collaboration across study teams. These skills and qualifications are essential for maintaining study integrity, regulatory compliance, and successful clinical trial outcomes.

What are some common challenges faced by clinical research professionals at Tandem Clinical Research, and how can they be addressed?

Clinical research professionals at Tandem Clinical Research often encounter challenges such as managing multiple studies simultaneously, ensuring strict adherence to regulatory requirements, and coordinating effectively with cross-functional teams. To address these challenges, strong organizational skills, clear communication, and continuous training in compliance protocols are essential. Additionally, Tandem fosters a collaborative work environment where team members can share best practices and support each other, helping to navigate the complexities of clinical trials more efficiently.

What is the difference between Tandem Clinical Research vs Clinical Research Coordinator?

AspectTandem Clinical ResearchClinical Research Coordinator
CertificationsOften requires GCP training, clinical research certificationsTypically requires GCP training, certification varies
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesHospitals, research sites, clinics
Job ResponsibilitiesOversees clinical trials, manages data, ensures complianceCoordinates trial activities, enrolls patients, collects data

Both roles involve clinical trial activities, but Tandem Clinical Research often focuses on managing and overseeing trials within CROs or pharmaceutical companies, while Clinical Research Coordinators typically handle the day-to-day operations at research sites. Understanding these differences can help job seekers identify the right career path in clinical research.

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What cities are hiring for Tandem Clinical Research jobs?

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What states have the most Tandem Clinical Research jobs?

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Tandem Clinical Research jobs near you
Infographic showing various Tandem Clinical Research job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 5% Part Time, and 5% Temporary. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Tandem Intermediate LLC

Metairie, LA • On-site

Full-time

Re-posted 21 days ago

Key responsibilities

  • Assist in the daily activities of clinical research studies and clinic operations.

  • Collect, process, and ship laboratory samples according to study requirements.

  • Support study coordination by maintaining regulatory records and assisting with documentation.

Job description

Description

The Clinical Research Assistant (CRA) assists in the daily activities of clinical research studies and clinic operations. This role involves working closely with clinical teams, investigators, and study participants to ensure that all required procedures and visits occur according to protocol-specific guidelines.

Key Responsibilities:

  •  Study Familiarization: Thoroughly understand assigned studies by reading protocols, attending start-up meetings, and coordinating with the Principal Investigator and study team.
  •  Protocol Adherence: Ensure strict adherence to study protocols and obtain exemptions when applicable.
  •  Specimen Collection & Processing: Collect, process, and ship laboratory samples in accordance with study requirements.
  •  Patient Screening & Qualification: Collect initial psychiatric and medical information through patient interviews and access appropriate sources to qualify and accurately place patients in enrolling clinical trials.
  •  Study Coordination Support: Assist Clinical Research Coordinators in trial-related organization and documentation, including filing and maintaining regulatory records.
  •  Communication & Reporting: Communicate protocol issues to the study team, Site Administrator, Principal Investigator (PI), or Sub-Investigator as needed.
  •  Clinical Tasks: Perform clinical tasks such as vital signs measurement, height and weight recording, ECG administration, phlebotomy, and specimen packaging.
  •  Documentation & Compliance: Maintain timely source documentation and ensure compliance with sponsor-required information.
  •  Patient Education: Educate patients and their families about study participation and clinical drug trials in general.
  •  Community Engagement: Assist in community outreach events and provide appropriate community resource referrals to patients, caretakers, and family members when applicable.
  •  Additional Duties: Perform ad-hoc tasks and assist in other study-related activities as needed.

Additional Responsibilities:

This job description outlines the primary responsibilities of the Clinical Research Assistant; however, additional duties may be assigned as needed to support the research program or the operational needs of the organization. These additional responsibilities are not limited to the above and may evolve over time based on study requirements or business needs.

Requirements

Knowledge, Skills, and Abilities:

  •  Communication: Ability to communicate effectively (both written and oral) with patients, study teams, and external stakeholders.
  •  Interpersonal Skills: Excellent interpersonal and customer service skills to engage with study participants and colleagues.
  •  Organizational Skills: Strong ability to prioritize tasks, manage multiple responsibilities, and maintain documentation.
  •  Technical Proficiency: Proficiency in Microsoft Office software required; knowledge of Electronic Medical Records (EMR) systems preferred.
  •  Attention to Detail: High level of accuracy in maintaining documentation and following protocol guidelines.
  •  Team Collaboration: Ability to work independently and collaboratively within a multidisciplinary team.
  •  Confidentiality: Ability to handle sensitive participant data while adhering to ethical and regulatory guidelines.

Required Experience and Qualifications:

  •  Education: Bachelor's degree preferred.
  •  Experience: Previous experience in a healthcare or clinical research setting is a plus.
  •  Clinical Trials Knowledge: Previous exposure to clinical trials is preferred but not required.

This role is ideal for someone detail-oriented, organized, and eager to support clinical research in advancing medical knowledge and patient care.

Apply