Drug Safety Associate

Actalent; Deutschland; Hybrid; EUR 17.000 - 27.000; Vollzeit

Zusammenfassung

Actalent is seeking a Junior Drug Safety Associate to support pharmacovigilance and patient safety initiatives. The role focuses on adverse event processing, data integrity, and regulatory compliance in a collaborative, quality-driven environment.

The position offers a hybrid work setup with potential on-site collaboration at the Port Washington facility, supporting case management and database updates while developing expertise in drug safety and regulatory practices.

Qualifikationen

• Bachelor's degree in Life Sciences, Biology, Healthcare, or a related field preferred.
• Strong attention to detail and commitment to data accuracy.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office applications, including Word, Excel, and Outlook.
• Experience working with databases, electronic records, or structured data entry systems.
• Ability to manage multiple priorities in a fast-paced, deadline-driven environment.
• Strong organizational and problem-solving skills.
• Ability to follow established procedures in a highly regulated environment.

Aufgaben

• Receive and process adverse event reports, technical complaints, and medical inquiries via phone, email, and other channels.
• Perform case intake, triage, and tracking to ensure safety reports are handled accurately and efficiently.
• Enter and maintain case information within pharmacovigilance databases.
• Document safety information clearly and in accordance with procedures.
• Coordinate routing of cases and documentation to internal stakeholders.
• Conduct quality checks to ensure case files are complete and compliant before submission.

Kenntnisse

Attention to detail

Communication skills

MS Office proficiency

Data entry systems

Multi-tasking

Organizational skills

Regulated environment

Ausbildung

Bachelor's degree in Life Sciences or related field

Tools

Databases

Jobbeschreibung

Junior Drug Safety Associate

Launch Your Career in Pharmacovigilance and Patient Safety

Are you passionate about healthcare, life sciences, and making a meaningful impact on patient safety? We are seeking a detail-oriented Junior Drug Safety Associate to join our growing pharmacovigilance team. This is an excellent opportunity for recent graduates and early-career professionals looking to build a career in drug safety, pharmaceutical operations, and regulatory compliance.

In this role, you'll play a critical part in supporting the monitoring and reporting of product safety information, helping ensure that patients, healthcare providers, and regulatory authorities receive accurate and timely safety data. You'll work alongside experienced drug safety professionals in a collaborative environment that values quality, precision, and continuous learning.

What You'll Do

• Receive and process adverse event reports, technical complaints, and medical inquiries through phone, email, and other communication channels.
• Perform case intake, triage, and tracking to ensure safety reports are handled accurately and efficiently.
• Enter and maintain case information within pharmacovigilance and adverse event databases.
• Document safety information clearly, accurately, and in accordance with established procedures.
• Coordinate the routing of cases and supporting documentation to internal stakeholders.
• Conduct quality review checks to ensure case files are complete, accurate, and compliant before submission.
• Follow up on outstanding cases to obtain missing information and ensure timely case closure.
• Manage safety databases, shared mailboxes, and electronic records to support operational efficiency.
• Coordinate translation services for reports received in non-English languages.
• Assist with the development and maintenance of standard operating procedures and process improvements.
• Support compliance with pharmacovigilance regulations, company policies, and industry best practices.

What We're Looking For

Required Qualifications

• Bachelor's degree in Life Sciences, Biology, Healthcare, or a related field preferred.
• Strong attention to detail and commitment to data accuracy.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office applications, including Word, Excel, and Outlook.
• Experience working with databases, electronic records, or structured data entry systems.
• Ability to manage multiple priorities in a fast-paced, deadline-driven environment.
• Strong organizational and problem-solving skills.
• Ability to follow established procedures and work effectively in a highly regulated environment.

Preferred Qualifications

• Exposure to pharmacovigilance, drug safety, adverse event reporting, or regulatory affairs.
• Experience in customer service, call center operations, medical information, healthcare, or pharmaceutical environments.
• Familiarity with safety databases and adverse event tracking systems.
• Experience handling medical inquiries or product complaints.
• Background in biology, life sciences, healthcare, or related disciplines.
• Experience collaborating with cross-functional teams and stakeholders.

Why Join Us?

• Gain valuable experience in the pharmaceutical and life sciences industry.
• Develop expertise in pharmacovigilance, drug safety, and regulatory compliance.
• Work alongside experienced professionals dedicated to patient safety.
• Build transferable skills in case management, compliance, quality assurance, and medical communications.
• Enjoy a collaborative, supportive environment with opportunities for professional growth and development.
• Make a meaningful contribution to the safety of healthcare products used by patients worldwide.

Work Environment

This is a primarily remote position with occasional on-site attendance at the Port Washington facility for team meetings and company events, typically once or twice during the contract period. The role utilizes Microsoft Office, safety databases, and communication platforms extensively and operates within a structured, quality-focused environment where accuracy, compliance, and attention to detail are essential.

Take the Next Step in Your Career

If you're looking to start or advance your career in pharmacovigilance and want to contribute to patient safety while growing in a dynamic pharmaceutical environment, we'd love to hear from you. Apply today and become part of a team committed to protecting patient health and maintaining the highest standards of drug safety.

Job Type & Location

This is a Contract position based out of Port Washington, NY.

Pay and Benefits

The pay range for this position is $20.00 - $23.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your jobclassification and length of employment. Benefits are subject to change and may besubject to specific elections, plan, or program terms. If eligible, the benefitsavailable for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Port Washington,NY.

Application Deadline

This position is anticipated to close on Sep 11, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.