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Entry Pharmacovigilance Jobs (NOW HIRING)

Evolution Research Group

Data Entry Coordinator

Miami, FL · On-site

$18 - $22/hr

S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic ... As a Data Entry Coordinator, you will be responsible for the overall coordination, organization ...

Quotient Sciences

Data Entry Coordinator

Miami, FL · On-site

... pharmacology, clinical trials, and commercial product manufacturing. Our proprietary and disruptive platform - "Translational Pharmaceutics ® " - integrates Drug Product Manufacturing and Clinical ...

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How much do entry pharmacovigilance jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for entry pharmacovigilance in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What is an entry pharmacovigilance job?

Entry-level pharmacovigilance jobs are positions for individuals who are new to the field of drug safety and monitoring. These roles typically involve tasks such as collecting and processing reports of adverse drug reactions, maintaining safety databases, assisting in regulatory submissions, and supporting senior staff in ensuring compliance with pharmacovigilance regulations. Entry-level professionals in this field play an important role in ensuring the safety of pharmaceutical products and protecting public health, often working under the supervision of more experienced pharmacovigilance team members.

What are the key skills and qualifications needed to thrive as an entry pharmacovigilance professional?

To thrive as an Entry Pharmacovigilance professional, you need a background in life sciences or pharmacy, strong analytical abilities, and attention to detail. Familiarity with pharmacovigilance databases (like Argus Safety), regulatory reporting systems, and Good Pharmacovigilance Practices (GVP) guidelines is important. Excellent written communication, teamwork, and problem-solving skills help you effectively report and assess adverse drug reactions. These skills ensure compliance with regulatory standards and the safety of pharmaceutical products for public health.

What are some typical challenges faced by professionals starting out in an entry pharmacovigilance role?

Entry-level pharmacovigilance professionals often encounter challenges such as learning to interpret complex medical data and mastering specialized safety databases. Adapting to strict regulatory timelines and ensuring accuracy in adverse event reporting are also common hurdles. Additionally, effective collaboration with cross-functional teams—such as regulatory affairs and clinical research—may require developing strong communication and organizational skills. Over time, gaining familiarity with global pharmacovigilance regulations and standard operating procedures helps build confidence and expertise in the role.

What is the difference between Entry Pharmacovigilance vs Entry Medical Writer?

AspectEntry PharmacovigilanceEntry Medical Writer
Required CredentialsBachelor's degree in life sciences, pharmacology, or related field; training in pharmacovigilanceBachelor's degree in life sciences, healthcare, or related; strong writing skills
Work EnvironmentPharmaceutical companies, CROs, regulatory agenciesPharmaceutical companies, medical communication agencies, CROs
Industry UsageMonitoring drug safety, adverse event reportingCreating clinical study reports, regulatory documents

Entry Pharmacovigilance focuses on monitoring drug safety and adverse event reporting, while Entry Medical Writer specializes in preparing clinical and regulatory documents. Both roles require a background in life sciences and are common entry points in the pharmaceutical industry, but they differ in daily tasks and skill sets.

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Entry Pharmacovigilance jobs near you
Infographic showing various Entry Pharmacovigilance job openings in the United States as of August 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Data Entry Coordinator

Miami, FL • On-site

Evolution Research Group
See more jobs at Evolution Research Groupexternal

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Re-posted 29 days ago

Job description

Data Entry Coordinator

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

We are seeking a highly organized and detail-oriented Data Entry Coordinator to join our team. As a Data Entry Coordinator, you will be responsible for the overall coordination, organization, and efficient implementation of clinical data. Complete all study related data entry procedures under the direction of the Site Director. Maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Data Entry Coordinator is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, and company standard operating procedures and policies.

Responsibilities:

  • Performing data entry tasks with a high degree of accuracy and efficiency
  • Responsible for clinical data processing as directed by Site Director or another assigned manager. Quality control the clinical data to ensure the data quality and report discrepancies to the coordinator.
  • Complete any training as required by sponsor for access and approval to complete data entry.
  • Enter data as appropriate for protocol into paper or electronic case report forms.
  • Track to ensure that data entry is complete for subjects including completed study visits and related forms.
  • With CRC and/or manager oversight assist Sponsor or CRO data manager with resolution of queries to ensure clinical data quality.
  • Study, learn, and comply with ERG standard operating procedures and other policies, practices, and regulations where applicable.

Minimum Qualifications:

  • High school diploma or equivalent
  • Proven experience in data entry or a related field
  • Proficiency in word processing and database applications
  • Excellent attention to detail and accuracy
  • Strong organizational and time management skills

Preferred Qualifications:

  • High School Diploma or equivalent
  • Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
  • Experience working in a clinical or research environment

Apply