ZipRecruiter

Log In

Nucleus Global

60 Nucleus Global Jobs Hiring Near You

Red Nucleus

Clinical Research Scientist

Princeton, NJ · On-site

... global regulatory and post-market surveillance requirements. Responsibilities include: * Work ... Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared ...

Ashfield MedComms

Senior Account Manager

We are part of Inizio Medical, which also includes ApotheCom, Nucleus Global and MEDiSTRAVA. Our position as part of this international network gives us a key advantage over other agencies in terms ...

Ashfield MedComms

Senior Account Manager

OR · On-site +1

We are part of Inizio Medical, which also includes ApotheCom, Nucleus Global and MEDiSTRAVA. Our position as part of this international network gives us a key advantage over other agencies in terms ...

Red Nucleus

Clinical Research Scientist

Princeton, NJ · On-site

$110 - $160/hr

... global regulatory and post-market surveillance requirements. Responsibilities include: * Work ... Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared ...

Rednucleus

Sr Commercial Consultant

Boston, MA

Our global team is composed of nearly 1,000 full-time employees whose commitment to creativity, quality, and on-time delivery is unrivaled in our space. At Red Nucleus, we believe in providing a rich ...

TekWissen LLC

Sr. Formulation Technician

Austin, TX · On-site

$25 - $26/hr

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that ... Isolate and dilute nucleic acids using pipetting and spectrophotometric techniques. * Perform ...

previous page

Showing results 41-60

All JobsNucleus Global Jobs

Nucleus Global Jobs Information

Infographic showing various job openings at Nucleus Global in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 13% Physical, and 87% Remote job distribution.

Clinical Research Scientist

Red Nucleus

Princeton, NJ • On-site

Full-time

Posted 13 days ago

Job description

The Clinical Research Scientist will be responsible for the development of post-market clinical research strategies of orthopedic devices to support global regulatory and post-market surveillance requirements.
Responsibilities include:
  • Work closely with cross-functional teams (Clinical, Medical, Regulatory, R&D, Marketing) to develop post market clinical evidence generation strategies that consider evidence needs for EU Medical Device Regulations (EU MDR). Facilitate clinical evidence reviews with cross functional team to align clinical evidence strategies, document / track decisions and risks, and write PMCF Plans.
  • Develop and write high quality Post-market Clinical Follow-up (PMCF) plans and reports with minimal supervision. Support development and drafting of clinical study protocols, registry plans, epidemiology studies, informed consents, investigator brochures, and other study materials where needed.
  • Review summaries of clinical evidence and PMCF strategies in other areas of the Technical Documentation for accuracy and completeness. This includes the Clinical Evaluation Plan, Clinical Evaluation Report (CEP), Post Market Surveillance Plan and Periodic Safety Update Report (PSUR).
  • Where required, foster relationships with surgeons, hospitals and research teams to gain input into study design, evaluate study feasibility, and identify sites for study execution or data collection. Develop strong collaborative relationships with the study core team and others to ensure study progress for assigned projects and that issues are identified and communicated to leaders.
  • Partner with the Contracts and Payments team to ensure timely execution of all study agreements and corresponding payments for achieved milestones and deliverables.
  • Support clinical scientific discussions with internal stakeholders within Clinical, Medical, Regulatory, R&D and Marketing to drive support of the clinical and regulatory strategy, communicate evidence needs.
  • Contribute to appropriate interpretation and dissemination of all evidence generated, including abstracts, manuscripts, and Clinical Study Reports (CSR), epidemiology study results and clinical literature.
  • Develop a strong understanding of the orthopedic device product portfolio and business needs for clinical evidence to meet regulatory requirements.

Qualifications:
  • A Master's degree in Biological Science or related discipline, with a minimum of 4 years' experience in the medical device industry or healthcare field is required
  • Advanced technical writing skills is required, with demonstrated experience in writing PMCF plans / reports strongly preferred.
  • Clinical expertise in the medical device sector
  • Proven experience in conducting clinical studies, registries particularly in the field of orthopaedics
  • Strong project management skills required, with demonstrable track record of success managing multiple projects simultaneously with minimal supervision.
  • Excellent communication skills, including effective interaction with healthcare professionals (HCPs), hospital staff etc.

Diversity, equity and inclusion are valued at Red Nucleus and we believe we have a shared responsibility to provide equal opportunity and foster an inclusive spirit. We do not discriminate on the basis of race, color, national origin, religion, caste, sexual orientation, gender, age, marital status, veteran status, or disability status.
To learn more about working at Red Nucleus, please visit Careers | Red Nucleus.
#LI-KS1

Apply