1

Biotech Data Entry Jobs in East Rutherford, NJ (NOW HIRING)

Records and Statistical Clerk

Newark, NJ

$17.25 - $22.75/hr

... biotechnology and medicine, environmental and occupational health, and health care policy and aging ... Must have three (3) full years of clerical experience performing data entry activities, database ...

... biotechnology and medicine, environmental and occupational health, and health care policy and aging ... Must have three (3) full years of clerical experience performing data entry activities, database ...

... biotechnology and medicine, environmental and occupational health, and health care policy and aging ... person intakes and labs, data entry, document management, and various research-related ...

Dental Assistant

Newark, NJ ยท On-site

$24.83/hr

... biotechnology and medicine, environmental and occupational health, and health care policy and aging ... front desk and data entry. Essential Duties and Responsibilities include the following:

Student Assistant

Newark, NJ ยท On-site

$15.92/hr

... biotechnology and medicine, environmental and occupational health, and health care policy and aging ... Support Data Collection and Entry: Assist with gathering, entering, and managing data to ensure ...

Obtain entry and access permits * Support environmental permitting tasks if requested * Support ... data for various environmental impact projects Required; OR * Master's Degree in Environmental ...

Key Account Manager - New York

New York, NY ยท On-site

$200K - $240K/yr

Data-Driven Account Management * Leverage multiple data sources (sales, market, utilization, and ... biotech, or healthcare sales experience. * 3-5 years of experience with complex access environments ...

Key Account Manager - New York

New York, NY ยท On-site

$200K - $240K/yr

Data-Driven Account Management * Leverage multiple data sources (sales, market, utilization, and ... biotech, or healthcare sales experience. * 3-5 years of experience with complex access environments ...

... order entry, and customer follow-up. Duties and Responsibilities: * Perform and support all ... S. in Biomedical Engineering, Biotech, Electrical Engineering, or Electronics related fields or ...

next page

Showing results 1-20

Biotech Data Entry information

See East Rutherford, NJ salary details

$11

$19

$28

How much do biotech data entry jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for biotech data entry in East Rutherford, NJ is $19.84, according to ZipRecruiter salary data. Most workers in this role earn between $16.63 and $22.31 per hour, depending on experience, location, and employer.

What are Biotech Data Entry jobs?

Biotech Data Entry jobs involve inputting, managing, and updating data related to biological or pharmaceutical research, clinical trials, laboratory results, and other scientific information. Professionals in this role ensure the accuracy and integrity of data by following strict protocols and using specialized software. They work closely with scientists, researchers, and regulatory teams to maintain databases that are essential for analysis, reporting, and compliance. Attention to detail, familiarity with scientific terminology, and proficiency in data management tools are key skills for this job.

What is the difference between Biotech Data Entry vs Laboratory Data Technician?

AspectBiotech Data EntryLaboratory Data Technician
Required CredentialsHigh school diploma or equivalent; basic computer skillsAssociate's degree or certification in laboratory technology
Work EnvironmentOffice or remote data entry settings within biotech companiesLaboratory settings with hands-on sample handling
Employer & Industry UsageBiotech firms, research organizationsResearch labs, pharmaceutical companies
Common Search & ComparisonYesYes

Biotech Data Entry primarily involves inputting and managing data related to biotech research, often in office or remote settings. Laboratory Data Technicians perform hands-on sample processing and data collection in lab environments. While both roles support biotech research, Data Entry focuses on data management, whereas Laboratory Data Technicians handle physical samples and lab procedures.

What are the key skills and qualifications needed to thrive as a Biotech Data Entry professional, and why are they important?

To thrive as a Biotech Data Entry professional, you need strong attention to detail, data accuracy, and basic knowledge of biological terminology, often supported by an associate's degree or relevant coursework. Familiarity with laboratory information management systems (LIMS), spreadsheet software like Microsoft Excel, and data validation tools is typically required. Excellent organizational skills, time management, and the ability to work both independently and collaboratively help individuals excel in this role. These skills ensure accurate data recording and management, which is critical for regulatory compliance and the integrity of research and development processes.

What are some common challenges faced in a Biotech Data Entry role, and how can they be managed?

One common challenge in Biotech Data Entry is ensuring the accuracy and integrity of complex scientific data, as errors can impact research outcomes or regulatory compliance. Managing large volumes of information from various sources can also be overwhelming, especially when adhering to strict deadlines. To address these challenges, professionals often rely on standardized protocols, validation checks, and regular communication with researchers or lab staff to clarify uncertainties. Gaining familiarity with specialized data management software and prioritizing tasks can further help maintain efficiency and data quality.
What are popular job titles related to Biotech Data Entry jobs in East Rutherford, NJ? For Biotech Data Entry jobs in East Rutherford, NJ, the most frequently searched job titles are:
What cities near East Rutherford, NJ are hiring for Biotech Data Entry jobs? Cities near East Rutherford, NJ with the most Biotech Data Entry job openings:

Clinical Product Management Specialist - Onsite

millenniumsoft

Franklin Lakes, NJ โ€ข On-site

Full-time

Posted 26 days ago


Job description

Position : Clinical Product Management Specialist
Location : Franklin Lakes, NJ
Duration : 7 Months
Total Hours/week : 40.00
1st Shift
Client : Medical Devices Company
Job Category : Clinical
Level of Experience : Senior Level
Employment Type : Contract on W2 (Need US Citizens or GC Holders or GC EAD or OPT or EAD or CPT
JOB DESCRIPTION
  • The Clinical Product Management Specialist is responsible to provide product procurement, handling, inventory management, and shipment services to their assigned projects/Business Units studies.
  • They will work closely with the Clinical Project Manager and Medical Affairs to fulfill their study product related deliverables in conjunction with the client Quality Management system SOPS and regulatory requirements.

Job Responsibilities: (Primary Duties, Roles, and/or Authorities)
  • Collaborate with the Clinical Study team to include Medical Affairs, Clinical Product Management and other departments as required.
  • Develop clear and efficient study product secondary labeling and packaging designs to facilitate study execution, protocol compliance, and product accountability.
  • Responsible for researching products/potential vendors, researching/procuring study supplies, monitoring inbound shipments and cost accruals per study.
  • Maintain Study Product and Study Supply inventory using Inventory management database.
  • Inspect Study Product, including packaging and labeling per SOP and Study-specific requirements.
  • Accountable for assembly of kits, formatting and printing labels, over-labelling.
  • Oversee the storage of Study Product and Study Supplies under secure, controlled conditions which are compliant with GCP and other applicable regulations and guidelines, and which adhere to the required limits of temperature and humidity.
  • Complete the disposition of product and/or supplies returned at the end of each study, including destruction or restocking.
  • Responsible for packaging, shipping documentation and shipping of material (International, Domestic)
  • Tracking Documentation and filing in eTMF.
  • Responsible for Transparency Reporting for designated studies.

Education and Experience:
  • A minimum BA/BS in Science, Engineering, Pharmacy, or other Allied Health professions.
  • A minimum of 3 years' experience in Medical Device clinical trials, pharmaceutical, biotechnology or related firm, including direct exposure to the process of clinical study supply (IUO and Ancillary) management and execution.

Knowledge and Skills:
  • Knowledge of Good Clinical Practice (GCP), regulations and guidance relative to the conduct of clinical trials
  • Proficient in MS Word Processing (Mail Merge experience a plus), Spreadsheets (Must be able to use formulas in Excel) and Databases (front end data entry).
  • Strong English language written and verbal communication skills.
  • Knowledge of clinical supply planning, packaging, and labeling.
  • Clinical Study product handling experience is preferred.
  • Demonstrate experience in working on inventory management, and assembly of kits.
  • Highly organized, detail oriented, focused and creative.
  • Excellent interpersonal skills and communication skills.
  • Ability to perform under highly matrix environment, and able to thrive in a multidisciplinary team environment.
  • Must be computer savvy, detailed oriented, fast learner, and agile.
  • Database experience is a MUST.

Physical Demands: (if applicable)
  • Must be capable of lifting/moving up to 30lbs.
  • Repetitive motions with fingers/hands/wrists required for labeling and kitting products.
  • Must be able to sit for long periods of time.

Work Environment: (if applicable)
Onsite Position.
Office and laboratory/storage environment.