Medical Research Representative Job at iconplc (Salt Lake City)

Medical Sales Representative

Mantell Associates is currently partnered with a leading CDMO specializing in ge...

Location

Brazil

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotech, or related field
2-4 years of proven sales experience in pharmaceuticals, biologics, biotech, or medical devices
experience in CDMO or advanced therapy services is a strong plus
Solid understanding of biologics / gene therapy manufacturing services, GMP, regulatory / quality requirements, and value drivers in this specialized space
Strong interpersonal, presentation, and negotiation skills
ability to explain technical services to scientific and commercial audiences
Portuguese fluency required
English proficiency strongly preferred
ability to travel within assigned territory frequently
Based in Brazil, with legal authorization to work

Job Responsibility

Visit hospitals, clinics, biotech & pharmaceutical companies to promote the CDMO’s gene therapy / vector development / GMP manufacturing capabilities
Build and maintain strong relationships with Key Opinion Leaders, research institutions, procurement teams, and decision-makers in the gene therapy and advanced biologics space
Execute sales plans and develop territory strategies to meet or exceed revenue targets, proposals, and contract wins
Clearly communicate technical service offerings, differentiators, turnaround times, quality standards, and compliance credentials to prospective clients
Collaborate with Business Development, Technical/Process Development, Regulatory, and Quality teams to ensure proposals, quotations, and customer expectations are aligned with service and regulatory capabilities
Monitor competitive landscape, market trends, client needs, and customer feedback
feed insights back into marketing/sales strategy
Maintain accurate CRM records, sales forecasts, visit reports, and territory performance metrics

Fulltime

Patient Access Services Representative

The TMCOne Pulmonary specializes in Pulmonary and Sleep Medicine where each pati...

Location

United States , Tucson

Salary:

Not provided

Tucson Medical Center

Expiration Date

Until further notice

Requirements

High School diploma or General Education Degree (GED)
completion of vocational medical office training desired, or an equivalent combination of relevant education and experience
preferred one (1) year of medical office and/or hospital experience to include healthcare eligibility and benefit analysis or scheduling experience for diagnostic testing and/or surgery
some positions may require certification as a Medical Assistant (CMA)
knowledge of office management practices, including billing and scheduling within healthcare
knowledge of basic computer familiarity and experience and the ability to operate basic office equipment
knowledge of patient care protocols and practices
knowledge of general patient care practice, methods and regulations
skill in evaluating patient’s needs or following up with a care-giver and then providing follow up support to patients
skill in scheduling appointments and referrals

Job Responsibility

Assists medical care givers with patient management, tracking and monitoring requirements
answers phones, pre-screens using appropriate triage skills, within allowable parameters calls in prescription re-fills, calls patients with test results and schedules patients for next appointments
perform extensive centralized scheduling, insurance verification, referral, billing and payment posting responsibilities
exhibits excellence in customer service through appropriate attitude and interaction with all patients, visitors and staff
collects deposits or deductibles and advises patient or guarantor of insurance benefits and anticipated cost estimates
ensures completion of financial documentation in accordance with TMCH’s credit and collection policies
explains all necessary compliance forms and obtains patient signature as required for regulatory agencies
performs medical necessity screening and ensures compliance with system requirements
interacts with physicians and/or physicians’ office staff to secure diagnosis, procedure details or authorizations and information for denials as needed
uses medical terminology and scheduling knowledge to select correct procedure when scheduling and coordinates information with other departments as needed

Fulltime

Research Associate - Certified Phlebotomy Technician

Parexel Early Phase Clinical Unit supports the development of innovative new med...

Location

United States , Glendale

Salary:

20.00 - 26.00 USD / Hour

Parexel

Expiration Date

Until further notice

Requirements

Active CPT License in the state of CA is required
Customer service experience in a fast-paced environment
Experience working in a medical or clinical setting is highly preferred
Comfortable standing and walking for a prolonged period of time
B.S.+ in related life science field OR HS diploma/GED with relevant experience

Job Responsibility

Understand study protocols and be able to complete required medical procedures
Recruit study participants by calling the database, attending company sponsored community events, posting flyers
Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs
Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results
Prepare/monitor study supplies and stock levels in clinic/hospital
Label, inventory, and send plasma samples
Problem solves study participant issues as they arise
Ensure basic study participant safety is provided
Assist with Monitor visits (i.e., room set up, etc.)
Identify issues that need Sponsor approval and bring these to the attention of the CRC

What we offer

Extensive induction program and ongoing training
Opportunity for career growth and advancement internally
Eligible for shift differentials
Eligible for participation in annual performance-based bonus plan
Annual salary review
Additional total rewards incentives
Paid time off
401k match
Life insurance
Health insurance

Fulltime

Litigation Attorney

Our client is looking for a skilled Litigation Attorney to join their team in Ca...

Location

United States , San Francisco

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Active license to practice law in California and MUST reside in California
demonstrated experience in civil litigation with a strong track record of successful case outcomes
familiarity with medical malpractice litigation is preferred, but a willingness to learn is essential
excellent written and oral communication skills, with the ability to present arguments persuasively
strong organizational and time management abilities to handle a high-volume caseload
proficiency in legal research tools and case management software
ability to work independently and as part of a collaborative legal team
reside in the San Francisco Bay Area or nearby regions.

Job Responsibility

Handle a variety of civil litigation cases from inception to resolution, ensuring all processes meet high standards of attention to detail
develop and implement effective case strategies to achieve favorable client outcomes
represent clients in court proceedings, depositions, and mediations with professionalism and expertise
conduct thorough legal research and draft compelling pleadings, motions, and other legal documents
collaborate with team members to share insights and ensure comprehensive case preparation
manage client communications, offering clear updates and guidance throughout the legal process
utilize knowledge of medical malpractice litigation or demonstrate a willingness to learn and excel in this area
maintain compliance with all legal and ethical standards while managing multiple deadlines and priorities effectively.

What we offer

Medical, vision, dental, and life and disability insurance
eligibility to enroll in the company's 401(k) plan
access to free online training
competitive compensation.

Fulltime

Associate Director Biostatistics

Amgen is expanding its global Biostatistics capabilities, with Amgen India (AIN)...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate in Statistics/Biostatistics (or related subject with high statistical content) with at least 12+ years of post-graduate statistical experience in the pharmaceutical industry or medical research
Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with at least 16+ years of post-graduate statistical experience in the pharmaceutical industry or medical research

Job Responsibility

Provide sound statistical guidance to clinical development, reimbursement, and medical affairs
Oversee statistical contributions to protocols, randomization specifications, statistical analysis plans (SAPs), clinical study reports (CSRs), and key trial documents
Ensure alignment of study design and analysis with scientific rigor, regulatory requirements, and Amgen policies
Collaborate cross-functionally with global teams to deliver high-quality analyses, publications, and regulatory filings
Contribute to innovative trial designs, advanced methodologies, and process improvement initiatives
Execute biostatistical strategies across the product lifecycle, from early development through post-marketing
Provide consultancy and training to colleagues across R&D
Support governance of outsourced statistical activities, ensuring adherence to Amgen standards and regulatory compliance
Represent Biostatistics in cross-functional and external interactions (e.g., with regulatory agencies, investigators, or data monitoring committees)
Drive technology adoption leveraging AI capabilities to streamline statistician’s work

What we offer

Vast opportunities to learn and develop within our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Medical Advisor- Oncology

You will provide scientific medical support in oncology across the Philippines. ...

Location

Philippines , Manila

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Advanced degree in a relevant scientific or healthcare field (MD, PhD, PharmD, or equivalent)
Minimum 2 years’ experience in medical affairs, clinical practice, clinical research, or related roles with demonstrated scientific communication skills
Strong written and spoken English
Fluent Filipino/Tagalog or other local language skills are an advantage
Proven ability to present complex clinical data clearly to diverse audiences
Valid Philippines driver’s license and readiness for regular travel
Ability to work independently, manage a territory, and build trusted professional relationships

Job Responsibility

Build and maintain trusted scientific relationships with oncologists and multidisciplinary healthcare teams
Respond to non-promotional medical information requests with accurate, balanced and clear explanations of clinical evidence
Collect and share clinical insights from the field to inform medical strategy and research priorities
Support clinical development activities, including identification and engagement of potential clinical trial sites and investigator-initiated studies
Represent the medical team at scientific meetings, conferences, and local events
Work closely with cross-functional partners to align medical, clinical and commercial activities around patient needs

What we offer

Opportunity to deepen your oncology expertise and influence medical strategy
Direct impact on clinical research and patient care in the Philippines
Collaborative, supportive team that values learning and growth

Fulltime

RN Research Screening Coordinator

The Screening Coordinator works directly with the physician to acquire required ...

Location

United States , Naples

Salary:

Not provided

NCH Healthcare System

Expiration Date

Until further notice

Requirements

Minimum of 3 years of hospital based medical experience is required
Licensed as a Registered Nurse (RN) in the State of Florida
Basic Life Support (BLS) certification required from the American Red Cross or American Heart Association
Trained or willing to be trained in phlebotomy, sample preparation and shipping, and EKG acquisition
Communication and Problem-Solving skills and ability to maintain flexibility
Intermediate computer knowledge: Uses Microsoft Word, Excel, Outlook, and Windows

Job Responsibility

Provides patient screening for all clinical trials, identifying candidates and securing physician approval as required
Updates all investigators on study design and eligibility criteria
Establishes an organized method and dialogue for approaching patients and explaining the required aspects of the trial, defining the reason they are being approached, and explaining the potential risks and benefits
Pre-screens all patients using available tools to assist physicians in patient identification
Promotes and encourages patient enrollment
Maintains a screening data base of both those patients participating and those who declined, and the reason for that decision
Determines the best method(s) to screen patients within the scope of each protocol and support of the physician
Utilizes required advertising as needed and approved by the IRB
Plans the implementation and execution of research protocols as it relates to patient enrollment and continuance
Prepares and reviews all materials to be used in the clinical trials

Fulltime

Senior Manager - Clinical Affairs

Define and lead the global Clinical Affairs strategy for Brainlab’s global surge...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Advanced scientific, medical or technical degree (PhD, MD, or equivalent preferred)
Extensive experience in Clinical Affairs, Clinical Research within the medical device industry
Strong background in clinical and regulatory requirements for Class I–III medical devices
Demonstrated leadership experience, including managing international or cross-functional teams
Several years of experience in Clinical Affairs, Clinical Research and/or R&D within the medical device industry
Clinical and regulatory background for Class I to Class III medical devices
In-depth knowledge of EU MDR, FDA regulations and Good Clinical Practice
Hands-on experience in clinical studies, clinical evaluations and regulatory submissions for medical devices
Ability to translate clinical research into scientific marketing content
Excellent stakeholder management, communication, and project leadership skills

Job Responsibility

Define and lead the global Clinical Affairs strategy for Brainlab’s global surgery portfolio, ensuring alignment with product, regulatory and commercial objectives / teams
Lead and develop an international Clinical Affairs team responsible for clinical evaluation, clinical research and scientific marketing communication
Ensure clinical compliance with EU MDR, FDA and other regulatory requirements
Build and maintain a strong clinical network of investigators, key opinion leaders and research partners
Act as Process Owner for clinical evaluation and validation, training authors and evaluators to ensure regulatory compliance
Partner closely with R&D, Product Management, Marketing, Sales and Quality Management on the strategy and to translate clinical insights into product innovation and market differentiation
Bridge clinical research and scientific marketing by translating evidence into credible, high-impact scientific and educational content
Ensure GDPR compliance in clinical collaborations
Define and manage clinical studies and investigations to support product innovation and regulatory approvals
Represent the company in communications with regulatory authorities related to clinical strategy, investigations and submissions

What we offer

30 vacation days, plus December 24th and December 31st
Flexible working hours
Hybrid work model within Germany
Bike leasing via cooperation partner "BikeLeasing"
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
Regular after work, team, and company events
Comprehensive training and continuing education opportunities

Fulltime

Medical Research Representative

iconplc

Location:
United States , Salt Lake City

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 02, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical Research Representative

Medical Sales Representative

Patient Access Services Representative

Research Associate - Certified Phlebotomy Technician

Litigation Attorney

Associate Director Biostatistics

Medical Advisor- Oncology

RN Research Screening Coordinator

Senior Manager - Clinical Affairs

Medical Research Representative

iconplc

Location:United States , Salt Lake City

Category:Research and Development

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 02, 2026

Looking for more opportunities? Search for other job offers that match your skills and interests.

Similar Jobs for Medical Research Representative

Medical Sales Representative

Patient Access Services Representative

Research Associate - Certified Phlebotomy Technician

Litigation Attorney

Associate Director Biostatistics

Medical Advisor- Oncology

RN Research Screening Coordinator

Senior Manager - Clinical Affairs

Location:
United States , Salt Lake City

Category:
Research and Development

Contract Type:
Not provided

Job Posted:
January 02, 2026