CrawlJobs Logo

Associate Clinical Business Development Executive

pci.com Logo

PCI Pharma Services

Location Icon

Location:
United States , Philadelphia

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

As an Associate, Business Development Executive your primary duty is to assist Business Development Executives in the daily management of accounts, with tasks including management and preparation for Quarterly Business Review Meetings, taking and providing comprehensive meeting notes during client meetings, direct management of smaller client accounts. You will also support the Lead Generation Manager in identifying potential global drug development targets, conduct research into their respective development pipelines, identify the appropriate contacts and work with the Business Development Executive/Manager located in the territory in which the target resides, to manage direct cold calls or mailers, or manage geography specific marketing lead campaigns.

Job Responsibility:

  • Assist Business Development Executives in the daily management of accounts
  • Management and preparation for Quarterly Business Review Meetings
  • Taking and providing comprehensive meeting notes during client meetings
  • Direct management of smaller client accounts
  • Support the Lead Generation Manager in identifying potential global drug development targets
  • Conduct research into their respective development pipelines
  • Identify the appropriate contacts and work with the Business Development Executive/Manager located in the territory in which the target resides
  • Manage direct cold calls or mailers, or manage geography specific marketing lead campaigns
  • Research various drug development companies, and update their information within SalesForce.com database
  • Making outbound calls to drug development companies including CROs, medical device, animal health and cell & gene therapy organizations
  • Attend client meetings, either face to face or via phone, generate comprehensive meeting minutes within two days of the meeting
  • Follow up on requests for information from clients and the Global BD team
  • Respond to inquiries that come in via email, the website, by phone and/or through trade shows
  • Assisting Business Development Executives in both the internal and external management and organization of Quarterly Business Review Meetings
  • Manage smaller, less complex accounts
  • Attend trade shows in a supportive capacity, if required
  • Manage PCI Site Visits, book rooms, organize internal attendees, collate slide decks and presentation materials
  • Attend PCI Site Meetings on behalf of the Business Development Executive (if appropriate)
  • Support and manage the submission of legal documentation such as CDAs or MSAs to both the PCI and Client legal teams

Requirements:

  • Ability to learn, understand and retain information regarding PCI Clinical Services offering
  • A great telephone personality for client contact
  • A motivated, positive and self-driven attitude
  • Highly organized, able to manage short to medium term projects
  • The desire to work independently without supervision, and from home
  • Problem-solving skills and the ability to overcome objections
  • An interest in the healthcare market
  • Intermediate to advanced Word, Powerpoint and Excel Skills
  • Experience using SalesForce.com software
  • Experience with outbound calling of any type which can include calls to customers, clients, members, alumni etc.
  • Ability to drive to client sites
  • Ability to travel greater than 40% of time

Additional Information:

Job Posted:
February 20, 2026

Expiration:
March 30, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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

Briefcase Icon

Similar Jobs for Associate Clinical Business Development Executive

Senior Business Development Manager or Associate Business Development Director

We are seeking an experienced Senior Business Development Manager or Associate B...
Location
Location
United States , New York, NY or Boston MA
Salary
Salary:
150000.00 - 180000.00 USD / Year
clicktherapeutics.com Logo
Click Therapeutics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s Degree Required
  • A minimum of 7 years of experience in life sciences industry
  • Licensing experience within pharma / biotech industry strongly preferred
  • Investment banking and/or strategy experience also acceptable
  • International or cross-border experience a plus
  • Strong grasp of the fundamentals of pharmaceutical drug discovery, development, and commercialization
  • An ambitious self-starter with a strong drive for achieving results
  • Track record of sourcing, negotiating, and closing partnerships with positive results
  • Extensive network of healthcare industry contacts
  • Ability to relate and work with wide range of colleagues across varied functions, experience levels and backgrounds (internally and externally) to achieve results
Job Responsibility
Job Responsibility
  • Build and manage a strong pipeline of deal opportunities that align with the strategic objectives of the company
  • Lead end-to-end deal processes, including sourcing, cross-functional diligence, structuring terms and driving negotiations
  • Identify and execute on creative opportunities to expand Click’s partnering presence in the industry
  • Contribute to broader business development strategy and direction beyond owned therapeutic areas
  • Develop and maintain strong relationships with potential partners and industry stakeholders
  • Represent Click at conferences, meetings and industry events
  • Develop a deep understanding of the science underlying Click’s mechanisms of action in owned therapeutic areas
  • Monitor industry trends, competitive landscape, clinical news and deal activity within owned therapeutic areas
What we offer
What we offer
  • Medical, Dental, & Vision Insurance
  • 401k Employer Matching up to 5%
  • One Medical membership
  • Fertility Care & Family-Building Support
  • Professional Development Stipend
  • Unlimited PTO
  • Caregiving Benefit
  • Annual performance-based cash bonus
  • Generous equity package
  • Life Insurance
  • Fulltime
Read More
Arrow Right

Business Development Associate

This role is responsible to drive sales, expand market share and increase produc...
Location
Location
Singapore
Salary
Salary:
Not provided
avanos.com Logo
Avanos
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Candidate with Nursing, Biomedical, Biotechnology or Science background preferred
  • At least 5 years of experience in related experience
  • Track record of profit/margin maximization, revenue growth, execute programs, manage projects and campaigns
  • Possess product training experience to clinical users and distributors
  • Strong understanding and identification of customers and their needs, clinical environment, competitive landscape and trends
  • Experience creating clinical acceptance and drive adoption of new treatments/therapies/technologies
  • Broad-based knowledge of medical consumables sales and marketing processes
  • Highly self-motivated, results-oriented with a drive and passion to succeed
  • Exceptional people skill and customer service oriented
  • Good communication and presentation skills
Job Responsibility
Job Responsibility
  • Drive sales, expand market share and increase product branding and awareness for the Company’s best-in-class products and business in assigned markets within Central Asia, mainly in Singapore
  • Participate in clinical cases, cadaver workshops and conferences
  • Perform equipment in-service maintenance and monitoring
  • Deliver product trainings to internal and external stakeholders e.g. sales team, physicians, clinical users, distributors, etc. to ascertain a solid understanding of AVANOS products, relevant technologies and application
  • Support operating procedures in the hospitals
  • Work closely with the Business Development Manager, Central Asia, ASEAN Sales Team, APAC Marketing Team to ensure the alignment of global, regional and local strategies, with the aim to elevate the company’s brand and improve product adoption efficacy through driving demand, sales and market expansion in the assigned markets
  • Work closely with cross-functional teams to own and drive customer satisfaction, product compliance, innovation and margin improvement
  • Be responsible for leading and building the Avanos Pain business mainly in Singapore
  • Achieve and exceed regional sales and financial budget and operational objectives
  • Drive growth on strategic focus products via increasing brand awareness and customer loyalty to Avanos products
What we offer
What we offer
  • Comprehensive and competitive range of benefits
  • Total Rewards package encompasses everything you receive as an employee
  • your pay, health care benefits, retirement plans and work/life benefits
Read More
Arrow Right
New

Japan Clinical Leader

Responsible for clinical development of the assigned project in Japan under the ...
Location
Location
Japan , Tokyo
Salary
Salary:
Not provided
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Scientific background in education
  • >3 years or more experience in clinical development
  • Experience in clinical development
  • Thorough understanding of the processes associated with clinical and regulatory submissions
  • Skill to design and execute development strategies (e.g. advanced medical and pharmaceutical knowledge, skill to design development strategies, knowledge on clinical study operations including guidelines and SOPs, skill to think logically, innovatively, and flexibly, writing skills)
  • Leadership skills
  • Team building skills, networking skills
  • Negotiation skills, consensus building skills
  • Problem solving skills
  • Project management skills
Job Responsibility
Job Responsibility
  • Evaluate candidates for development in the assigned TA/DA from scientific and technical aspects and formulate an effective development plan for Japan with the JDL and the global team
  • Contribute to establishing the global development plan by discussing points to consider in developing the product (including biomarkers and diagnostics) and obtaining approval in Japan (e.g. medical practice, communication with the government) with the global team and considering strategies towards early launch
  • Establish good working relationships with internal and external stakeholders [e.g. key opinion leaders (KOL), academic society, patient group] to enhance the possibility of expedited development and early approval with the JDL and senior JCL
  • Lead Japan Development Team (JDT) and clinical studies of assigned project to success in cooperation with JDT and global team members
  • Communicate closely with the GCL and Clinicians in Worldwide Research and Development (WRD) and respective Business Units (BU) and build and execute an effective development strategy
  • Prepare high quality documents (e.g.study outline, briefing document, CTD, query response, publications) and review them
  • When a Clinical Scientist (CS) is assigned to the project, review the documents prepared by the CS (e.g. full protocol, informed consent document, investigator's brochure)
  • when a CS is not assigned, the JCL is responsible to prepare and review these documents
  • Contribute to the preparation of the risk management plan for J-NDA submission and other documents required after approval
  • Review clinical data and protocol deviations and determine necessary actions for clinical studies in which he/she is the Clinical Lead
  • Fulltime
Read More
Arrow Right

Director, Global Medical Lead – Lysosomal Storage Disorders

The Global Medical Lead, Director level, is a critical leadership role in Global...
Location
Location
Switzerland
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD, PhD, PharmD or other advanced life sciences degree required
  • Extensive industry experience, especially in Medical Affairs (≥ 7 years) and Clinical Development, ideally in global role with experience in Genetic Medicine or LSDs/Rare Disease inherited metabolic conditions
  • Ability to work, influence, and gain consensus across regions and cross-functional teams
  • Demonstrate solid understanding of cross-functional inter-dependencies across the drug development lifecycle
  • Excellent communication skills and a strong enterprise mindset required for problem solving and high-level presentations for senior executive staff review
  • US and international experience working in orphan or specialty markets
  • Knowledge and hands-on skills required to develop the strategy, framework, and scientific content for a wide range of post marketing studies
  • Knowledgeable and current in GCP guidelines and compliance rules globally
  • Clinical trial and publication experience is desirable
  • Track record of successfully influencing without authority, partnering across functions especially with but not limited to Commercial
Job Responsibility
Job Responsibility
  • In partnership with the Commercial organization, co-develops the Integrated Brand Plan (IBP), as core member of the 3M (Medical – Marketing – Market Access) Team
  • Offers scientific and medical expertise to inform the overall product strategy, contributing to clinical development, commercialization, and market access plans
  • Leads development, execution, and communication of the Global Medical Plan in collaboration with other internal stakeholders across BioMarin
  • Provides subject matter expertise as well as strategic leadership in key internal medical and clinical teams
  • Act as product and disease area expert and primary contact point for all global compound or disease area related issues both internally and for the external community
  • Partner with other departments, such as commercial, finance, and clinical development, to ensure that the medical affairs budget supports and aligns with overall business goals
  • Develop Medical Affairs launch strategy and roadmap and lead all Medical Affairs launch activities in collaboration with Commercial and other key stakeholders
  • Represent Medical Affairs in the development of regulatory documents and submissions
  • Represent Medical Affairs at FDA/EMA meetings
  • As a core member of the Integrated Evidence Team, contributes to the development of the integrated evidence package for therapeutic area
Read More
Arrow Right
New

Japan Clinical Leader

Responsible for clinical development of the assigned project in Japan under the ...
Location
Location
Japan , Tokyo
Salary
Salary:
Not provided
pfizer.de Logo
Pfizer
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Scientific background in education
  • >3 years or more experience in clinical development
  • Experience in clinical development
  • Thorough understanding of the processes associated with clinical and regulatory submissions
  • Skill to design and execute development strategies (e.g. advanced medical and pharmaceutical knowledge, skill to design development strategies, knowledge on clinical study operations including guidelines and SOPs, skill to think logically, innovatively, and flexibly, writing skills)
  • Strong leadership skills
  • Team building skills
  • Networking skills
  • Negotiation skills
  • Consensus building skills
Job Responsibility
Job Responsibility
  • Evaluate candidates for development in the assigned TA/DA from scientific and technical aspects and formulate an effective development plan for Japan with the JDL and the global team
  • Contribute to establishing the global development plan by discussing points to consider in developing the product (including biomarkers and diagnostics) and obtaining approval in Japan (e.g. medical practice, communication with the government) with the global team and considering strategies towards early launch
  • Establish good working relationships with internal and external stakeholders [e.g. key opinion leaders (KOL), academic society, patient group] to enhance the possibility of expedited development and early approval with the JDL
  • Lead Japan Medicine Team (JMT) and clinical studies of assigned project to success in cooperation with JMT and global team members
  • Communicate closely with GDL and Clinicians in Worldwide Research and Development (WRD) and respective Business Units (BU) and build and execute an effective development strategy
  • Prepare high quality documents (e.g. study outline, briefing document, CTD, query response, publications) and review them
  • Contribute to the preparation of the risk management plan for J-NDA submission and other documents required after approval
  • Review clinical data and protocol deviations and determine necessary actions for clinical studies in which he/she is the Clinical Lead
  • Review individual subject and cumulative safety data based on the safety review plan
  • Lead preparation of procedures related to independent data monitoring committee, adjudication committee, and safety review committee, and manage and execute the committees
  • Fulltime
Read More
Arrow Right

Senior Director, Global Medical Lead – Lysosomal Storage Disorders

The Global Medical Lead, Sr. Director level, is a critical leadership role in Gl...
Location
Location
Switzerland
Salary
Salary:
Not provided
biomarin.com Logo
BioMarin Pharmaceutical
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • MD, PhD, PharmD or other advanced life sciences degree required
  • Extensive industry experience, especially in Medical Affairs (≥ 7 years) and Clinical Development, ideally in global roles
  • Experience in LSDs/inherited metabolic conditions is desirable, either in pharmaceutical/clinical research or a clinical environment
  • Experience in Genetic Medicine is a plus
  • Ability to work, influence, and gain consensus across regions and cross-functional teams
  • Demonstrate solid understanding of cross-functional inter-dependencies across the drug development lifecycle
  • Excellent communication skills and a strong enterprise mindset required for problem solving and high-level presentations for senior executive staff review
  • US and international experience working in orphan or specialty markets
  • Have ability to design studies, develop protocols and monitor studies in a wide range of study types and phases including pre and post marketing
  • Knowledgeable and current in GCP guidelines and compliance rules globally
Job Responsibility
Job Responsibility
  • Leads development, execution, and communication of the Global Medical Plan in collaboration with other internal stakeholders across BioMarin
  • Provides subject matter expertise as well as leadership in key internal medical and clinical teams, called SMART teams, where s/he leads development of the medical plan and ensures that all critical components of medical plans are executed and monitored for the intended impact
  • Act as product and disease area expert and primary contact point for all global compound or disease area related issues both internally and for the external community
  • Develop Medical Affairs launch strategy and roadmap and lead all Medical Affairs launch activities in collaboration with Commercial and other key stakeholders
  • Represent Medical Affairs in development of regulatory documents and submissions (e.g. briefing books, protocols, label discussions etc.)
  • Represent Medical Affairs at FDA/EMA meetings
  • Leads the Integrated Evidence Team for development of the integrated evidence package for the therapeutic area. Ensures timely execution of the plan to ensure data gaps are filled optimizing patient access
  • Responsible for providing medical input into development, execution and interpretation of Clinical Development Plans, clinical protocols, including review of draft external research protocols, reports and manuscripts
  • Oversight of clinical registries and other post-marketing commitments
  • Evaluation of safety issues associated with product in collaboration with other departments
Read More
Arrow Right

Clinical Oncology Account Manager

The Clinical Oncology Account Manager is responsible for managing existing outpa...
Location
Location
United States , Dallas
Salary
Salary:
Not provided
questdiagnostics.com Logo
Quest Diagnostics
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Five or more years of sales experience in selling business to business with a history of documented sales success
  • Prior diagnostic or lab sales responsibility for closing new business and expanding existing relationships
  • Prior experience managing large multi-million-dollar specialty accounts
  • Prior experience with product launches in diagnostics and or lab
  • Prior experience selling to HCPs and account decision makers
  • prefer competitive market experience
  • Prefer hematology and oncology experience in healthcare, laboratory and/or diagnostics sales selling to medical professionals
  • Knowledge of Healthcare Industry and general economics of business
  • Ability to develop and sustain strong customer relationships
  • strong planning and organizational skills
Job Responsibility
Job Responsibility
  • Retain and grow oncology centers through identifying health plan leakage and up-selling the advanced oncology portfolio
  • Collaborate with the cancer center, medical affairs, pathologists to develop hematology and oncology clinical workflows to support the cancer center
  • Collaborate with precision oncology account executives, oncology business development executives, hospital account executives to support the collaborative selling model
  • Establish and strengthen support staff, lab managers, and HCP relationships with prospective customers within existing and new oncology accounts
  • Develop and execute access strategy for reach and frequency to oncology practice leadership
  • medical oncologists, hematologists, physicians, lab leadership, advanced access providers and support staff
  • Achieve call reach and frequency goals and targeting initiatives
  • Conduct quarterly clinical business reviews with oncology practices
  • include key matrix team members
  • Maintain and utilize Rx Vantage to support access to oncology practices
What we offer
What we offer
  • Medical, supplemental health, dental, and vision
  • 401(k) with company match up to 5% of annual salary
  • Virtual work options (hybrid, near-site, or fully remote)
  • Sales incentive plan (uncapped incentive paid out quarterly)
  • Comprehensive sales training program and educational assistance offerings
  • Company-supplied vehicle
  • Fulltime
Read More
Arrow Right
New

Clinical Analyst I or II - Radiology

Responsible for implementation and support of applications; works closely with e...
Location
Location
United States , Kansas City
Salary
Salary:
Not provided
kansashealthsystem.com Logo
The University of Kansas Health System
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Associates Degree in nursing or other clinical healthcare related field
  • 2 or more years of experience in clinical position (Nursing or Ancillary) in a health care institution or clinic
  • Current professional license or clinical certificate required in professional area
  • Certification or proficiency (with certification level score) in assigned Epic application or demonstrated learning of other assigned application must be obtained within 6 months of employment
Job Responsibility
Job Responsibility
  • Demonstrates accountability in delivering assigned task
  • reports project issues and accomplishments to project manager
  • delivers a work product that meets project requirements as defined by the scope and stays within departmental guidelines for application configuration/development
  • Analyzes and documents current and future needs and workflows through interviews and gathering data regarding regulatory requirements, operational procedures and hospital/departmental policies
  • Participates in the planning, development, implementation, maintenance, support and evaluation of clinical or business application systems as assigned
  • Develops relationships with the Nursing and Clinical communities
  • Participates/Contributes/Takes instructions in team and project meetings
  • works closely with team/department members on assignments
  • can work independently on some assignments
  • takes direction
  • Fulltime
Read More
Arrow Right