Sickle Cell Disease Educator Job at Randstad (Jabalpur)

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Miami/Tampa

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , DC/Baltimore/Richmond

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Atlanta; Raleigh

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Medical Science Liaison

This Director (or Associate Director) level MSL will own a defined US territory ...

Location

United States , Houston/Dallas

Salary:

180000.00 - 220000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Advanced scientific degree (PharmD, PhD, MD, or equivalent)
~10+ years industry experience in Medical Affairs with significant Field Medical tenure
Rare disease expertise required
hematology strongly preferred with emphasis on SCD
Small biotech experience preferred
demonstrated impact in resource‑constrained settings
Launch experience (pre‑approval to post‑launch), ideally in CGT or complex specialty (buy‑and‑bill) environments
Proven territory management and account planning capability across complex ecosystems (academic centers, community networks, payers, advocacy)
Independent, proactive operator with strong ownership
Cross‑functional collaboration with Clinical, Regulatory, Commercial, Medical Operations, and Publications while maintaining medical/scientific integrity

Job Responsibility

Develop and execute territory strategy: map treatment centers, referral networks, transplant/infusion sites, cell-collection capabilities, payers, and advocacy groups
prioritize accounts and set measurable objectives
Support treatment center onboarding: coordinate scientific and operational readiness aligned with SOPs, compliance, and patient journey requirements
partner with internal teams for qualification and activation
Build trusted relationships with KOLs and HCPs: deliver fair-balanced, evidence-based education on rare diseases, cell and gene therapy science, and Beam’s platform
foster advocacy and awareness
Educate stakeholders on disease state, therapeutic landscape, and company platform to drive awareness and credibility in the rare disease and CGT space
Generate high-quality insights from field interactions: synthesize trends and communicate actionable recommendations to Medical Affairs leadership and cross-functional partners
Collaborate on pre-launch planning: align with Medical Strategy, Publications, Medical Information, Value & Evidence, and Medical Operations to ensure scientific messaging, data dissemination, and field tools are ready for first commercial launch
Support clinical research activities: identify potential sites, assist with feasibility assessments, and promote best practices for enrollment and retention while maintaining medical/scientific independence

Fulltime

Senior Director, Gene Therapy Operations (Apheresis)

Beam is seeking a highly talented and motivated Senior Directory, Gene Therapy O...

Location

Salary:

260000.00 - 320000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor's degree or the combination of education and business experience required
Advanced degree preferred (e.g., MBA, RN, MPH, etc.)
Minimum 10+ years (18+ years) of healthcare or related experience, including significant experience within the biotech industry (especially with cell and gene therapy products)
Strong direct apheresis experience within the last 5 years
Strong preference for experience within Sickle Cell Disease and autologous cell & gene therapy
Qualification in Apheresis (QIA) certification preferred
Ability to work independently with very limited supervision
Ability to navigate and be successful in a fast-paced, highly matrixed work environment
Detail-oriented, able to assess and assimilate data and communicate objectively
Experience in commercial gene or cell therapy is greatly preferred

Job Responsibility

Develop and mentor a high performing Gene Therapy Operations, Apheresis team that is focused on delivering an excellent patient and stakeholder experience for commercial gene therapy from scheduling through infusion process
Develop and execute the strategic initiative and process for Treatment Center Qualification, training and ongoing support for patient coordination, scheduling, communication, cell collection support, and drug product infusion support
Drive Workflow & Training development: Design training to qualify apheresis and treatment centers, leading treatment center activation and certification processes and providing ongoing operational oversight post-activation
Quality & Compliance oversight: Ensuring compliance with regulatory standards (FACT, AABB), managing quality records (deviations, CAPAs, change controls) and overseeing the end-to-end process for patient apheresis and product delivery. Ensure COC/COI and assist in the implementation of ISBT-128 ST-018, as needed
Partner with Quality and Patient Operations team to build a robust treatment center network including center selection, qualification, training and ongoing support. Lead field team providing onsite support
Provide Apheresis expertise to support various internal activities and external facing training development
Create and conduct Apheresis and Cell therapy lab on-boarding, assessments, training, and collection support and other areas as needed
Build metrics program that will drive data collection and analysis in support of optimizing collection procedures, efficiency, and quality
Actively engage in the identification, sharing, and adaptation of best practices cross-functionally and between centers and identify and champion industry working group initiatives that will improve overall cell and gene therapy industry and treatment experience of our patients
Work closely across functions to ensure Chain of Identify and Chain of Custody are maintained throughout the patient journey

Fulltime

Health educator

Job Overview:As a SCD educator (Sickle Cell Disease Educator) your key role is t...

Location

India , Nagpur Bk

Salary:

Not provided

Randstad

Expiration Date

May 22, 2026

Requirements

Bachelor's degree in healthcare-related field (e.g., nursing, pharmacy, nutrition)
Preferred experience in rare diseases counseling or worked with health professionals
Strong preference for certification as a health educator (CDE)
1-2 years of education or counselling experience, ideally in pharmaceutical or healthcare setting
In-depth knowledge of rare diseases management and treatment options
Fluency in English, Hindi, and any other regional languages
Proficiency in MS Office

Job Responsibility

Provide tailored counseling to individuals with SCD and at the designated center
Educating individuals with SCD and their families or caregivers on SCD management, Future precautions in family planning, insulin/medicine/drug related education, treatment options, lifestyle adjustments, and diet plan

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New

Director, HCP Marketing

The Director, HCP Marketing will be a critical member of the Commercial team and...

Location

United States , Cambridge

Salary:

210000.00 - 260000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelor's degree with 10+ years of pharmaceutical or biotech experience, with at least 3 years focused on US HCP Marketing
Cell & Gene Therapies experience is strongly preferred
Experience supporting and partnering with field teams
Demonstrated ability to translate complex clinical information into clear, compelling promotional messaging for HCP audiences
Strong project management and organizational skills, with the ability to lead multiple high-priority initiatives simultaneously
Effectively managing external partners, agencies and budgets
Navigate Medical, Legal, and Regulatory (MLR) review and approval processes
Strong communication, strategic thinking, relationship-building skills, and a results-oriented mindset
Onsite requirements: Candidates are expected to come onsite 1-3 days per week

Job Responsibility

Responsible for the management of the agency of record, contributes to the development of brand strategy, develop and deploy unbranded and branded educational materials and engagement tools across personal and non-personal channels
Partner closely with account leads to align field strategies, deliver compelling resources, ensure consistent and aligned execution across regions
Create field-facing resources, engagement tools and training (e.g., leave-behinds, visual aids, digital content, trainings, etc.) that support effective HCP conversations and reinforce key messages
Lead the planning and execution of HCP-focused conference activities, including booth presence, branded and unbranded materials, and sponsored programs in collaboration with cross-functional teams
Drive the planning and execution of advisory boards including associated content development
Oversee tracking of HCP marketing budget accruals, forecasts, and actuals, and ensure successful and timely completion of projects within budget
Help manage external agencies and partners to ensure timely, high-quality deliverables that meet agreed-upon objectives, key performance indicators (KPIs), timelines, and budgets
Ensure compliance with all Medical, Legal, and Regulatory (MLR) requirements in the development and deployment of HCP-facing materials
Leverage customer and market insights, claims, and performance data to develop insight-driven marketing strategy and content, continuously optimize programs and identify opportunities for innovation

Fulltime

Social Worker - LCSW

The Licensed Clinical Social Worker (LCSW) at Memorial Primary Care supports the...

Location

United States , Pembroke Pines

Salary:

Not provided

Memorial Healthcare System

Expiration Date

Until further notice

Requirements

Masters (Required)
Fingerprint Screen (FINGERPRNT) - Florida Department of Childrens & Family (DCF)
Licensed Clinical Social Worker (SW LICENSE) - State of Florida (FL)
At least two (2) years post MSW experience in related field required
Previous experience working in hospital setting
Requires critical thinking skills, decisive judgment and the ability to work with minimal supervision
Must be able to work in a stressful and fast pace environment and take appropriate action

Job Responsibility

Participation in transplant selection committee meetings
Design and facilitate support groups and other programs
Attend multidisciplinary rounds as mandated by CMS for all Medicare-approved transplant centers and identifies appropriate resources for financial, insurance, transportation, housing, healthcare, mental health, spiritual services, and education about diagnosis and transplantation
Develop behavioral agreements with patient and/or families that addresses adherence and commitment to treatment plan
Assist with patient fund-raising
Assist patient in the comprehension of complex instructions, resolve conflicts, or facilities conflict resolution, have strong organization/ priority setting skills, must be able to learn and apply large amount of technical and procedural information, must be able to multi-task, and must be able to communicate effectively, verbally, and in writing
Interviews and assesses patients and/or family, caregivers, and/or legal representatives
Performs comprehensive psychosocial assessments for pre- post and living donors to determine transplant candidacy and continue to work with patient and family through all phases of the transplant process during inpatient and outpatient and end of life
Determines, prioritizes, provides and/or arranges for needed internal and external services/interventions
May supervise and/or train new staff, students, and interns

Fulltime

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Sickle Cell Disease Educator

Randstad

Location:
India , Jabalpur

Category:
Education

Contract Type:
Not provided

Salary:

Requirements:

Additional Information:

Job Posted:
May 19, 2026

Expiration:
July 06, 2026

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Sickle Cell Disease Educator

Randstad

Location:India , Jabalpur

Category:Education

Contract Type:Not provided

Salary:

Requirements:

Additional Information:

Job Posted:May 19, 2026

Expiration:July 06, 2026

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Job Posted:
May 19, 2026

Expiration:
July 06, 2026