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Manager Pharma Clinical Research Jobs (NOW HIRING)

Alcanza Clinical Research

Clinical Research Assistant

Katy, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA ...

NS Pharma Inc

Director, Clinical Research

Paramus, NJ · On-site

$210K - $240K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases ... Oversee, manage, and lead selection process of CROs for regional or global clinical studies.

Pinnacle Clinical Research

Clinical Research Coordinator

Austin, TX · On-site

$23.50 - $31.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Clinical Research Coordinator will manage the day-to-day operations of assigned clinical trials and ensure that pre-established work scope, study protocol, and regulatory requirements are ...

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How much do manager pharma clinical research jobs pay per year?

As of Aug 18, 2026, the average yearly pay for manager pharma 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 does a manager in pharma clinical research do?

A Manager of Pharma Clinical Research oversees the planning, execution, and management of clinical trials for pharmaceutical products. They ensure trials comply with regulatory guidelines, manage teams of clinical research associates, and coordinate with medical professionals, sponsors, and regulatory bodies. Their responsibilities also include monitoring trial progress, ensuring patient safety, and maintaining accurate documentation. This role is crucial in bringing new medications to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a manager in pharma clinical research?

To thrive as a Manager in Pharma Clinical Research, you need expertise in clinical trial design, regulatory compliance, and data analysis, often supported by a degree in life sciences or pharmacy and relevant clinical research certifications. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and Good Clinical Practice (GCP) guidelines is crucial. Strong leadership, problem-solving, and effective communication skills are essential for coordinating teams and liaising with stakeholders. These competencies ensure trials are conducted efficiently, ethically, and in compliance with regulatory standards, which is vital for successful drug development.

What are some common challenges faced by a manager in pharma clinical research, and how can these be addressed effectively?

Managers in Pharma Clinical Research often face challenges such as coordinating cross-functional teams, ensuring regulatory compliance, and managing tight project timelines. Balancing the needs of clinical sites, sponsors, and regulatory authorities can be complex, requiring strong communication and organizational skills. Proactively addressing these challenges involves fostering collaboration among team members, staying updated on regulatory changes, and implementing robust project management practices to keep studies on track and within budget.
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Manager Pharma Clinical Research jobs near you
Infographic showing various Manager Pharma Clinical Research job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Prolerity Clinical Research

Metairie, LA • On-site

Full-time

Re-posted 2 days ago

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.