Medical recruitment master Job at Myn

New

Senior Clinical Research Associate/Clinical Research Associate II - Oncology

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Preferred therapeutic experience in Oncology
Global clinical trial experience preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel (60-80%) within area is required
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites
Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
Provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F)
Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators
Partner with SCP and the study team to define and support recruitment initiatives at site level

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Fulltime

New

Study Delivery Sr Associate

The Study Delivery Senior Associate provides essential global study management s...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master's degree OR Bachelor's degree and 2 years of clinical execution experience OR Associate's degree and 6 years of clinical execution experience OR High school diploma / GED and 8 years of clinical execution experience
3 years' work experience in life sciences or medically related field, including 1 year of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
Experience working on global clinical trials
Strong collaborative and effective communication skills within a team environment
Understands importance of accuracy in documentation, data tracking, and compliance checks
Identifies discrepancies and escalates appropriately
Expertise in clinical trial processes, operations, and oversight in biotech, pharmaceutical, or Contract Research Organization environments
Strong skills in using MS Word, Excel, PowerPoint, and other relevant software for documentation, data management, and trial support
Working knowledge of CTMS, eTMF, EDC, and Microsoft Office tools
Ability to maintain accurate and timely data entry

Job Responsibility

Lead the development and maintenance of study-level trackers, dashboards, timelines, and tools (e.g., vendor management, sample tracking, drug supply planning) to ensure accuracy and visibility
Coordinate logistics for investigator meetings, trial events, and site communications
Manage assigned start-up activities, including system setup, access management, and document readiness, ensuring completion to required standards
Use study dashboards and reports to monitor global enrollment, data flow, and quality indicators, taking proactive action to address deviations and risks
Lead delivery of assigned risk and quality management activities
Track and report study progress, coordinating with Study team and vendors to resolve operational issues and maintain compliance
Deliver assigned components of global recruitment and retention strategies to help ensure enrollment targets are achieved
Manage Study Training system activities and oversight
Build and maintain effective relationships with internal study team members, vendors and investigator sites
Act as a point of contact for routine study updates, ensuring stakeholders are informed and aligned

New

Director, Care Management (RN or LCSW)

The Director, Care Management will mainly be responsible for the operational com...

Location

United States , Los Angeles

Salary:

135136.00 - 216218.00 USD / Year

L.A. Care Health Plan

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Nursing
Master's Degree in Social Work for Licensed Clinical Social Workers
Minimum of 7 years of Care Management experience including progressively responsible leadership experience facilitating quality/process improvement, updating policies/procedures with the latest regulatory and accreditation standards
At least 5 years of leading staff or supervisory/management experience
Minimum of 3 years of relevant Health Plan experience
Excellent verbal, written and presentation skills
Critical thinking skills
Ability to efficiently and effectively assimilate information and communicate clearly and promptly to key stakeholders
Ability to analyze and identify trends in reports to facilitate decision for enhancements to program
Proven effective leadership skills

Job Responsibility

Collaborating with the Medical Director, responsible for the operations, programming and oversight of internal L.A. Care's Care Management Department, collaborates with internal and external delegates and any operations associated with the Care Management department
Ensures the CM department performs the following: All contracts, regulations, applicable state and federal regulations, NCQA CM Certification, Management Services Agreements & Other Contracts
Oversees and monitors operational compliance with organizational standards, policies and procedures and regulatory requirements
Assures department meets all regulatory time frames on CM
Develops and implements departmental policies and procedures
Develops and maintains departmental statistical and performance reports
Develops, implements and monitors performance standards
Develops and maintains effective communication mechanisms at various levels of the organization and with external organizations
Develop and maintain departmental budgets in line with organizational goals
Assures appropriate staff support of Utilization Management and other relevant committees

What we offer

Paid Time Off (PTO)
Tuition Reimbursement
Retirement Plans
Medical, Dental and Vision
Wellness Program
Volunteer Time Off (VTO)

Fulltime

Zonal Sales Manager OC - West (Mumbai)

An exciting leadership opportunity to own and expand the West Zone business for ...

Location

India , Delhi NCR

Salary:

Not provided

Coloplast

Expiration Date

Until further notice

Requirements

Preferably a science graduate with Master’s in Sales
Over 12-18 years Sales Experience with a Multinational and Medical device company
Min. 7 years’ experience of leading a fast-paced growth oriented medical sales organization
Strong Analytical skills and proficient in MS Office Suite (Word, Excel, and PowerPoint) and SFDC
Intelligent demonstrated in test and business case understanding
Ability to motivate and lead a team with excellent coaching skills
Experience of handling several regions will be an added advantage
Proven Track record in demonstrating business results
Excellent communication and presentation skills
Experience in coaching a sales force

Job Responsibility

Provides leadership to the Zonal sales team in driving business results aligned to the KPIs
Provide strategic direction and guidance to the team in line with organization objectives
Responsible for recruiting, coaching, developing and managing the zonal ostomy sales team
Ensure sound distribution coverage and maximize sales execution
Responsible for achieving the given KPIs for the zone
Sets stretch objectives for the team and evaluates performance to drive continuous development
Dealer and Distribution Management and ensures 100% compliance
Provides timely coaching to RSM and sales force to maximize effectiveness
Develops Account Specific Action Plans (ASAP) together with the RSM and sales team for their respective high priority accounts
Drives the RSM to ensure that the sales team follows pre-defined call plan based on Segmentation and Targeting

Fulltime

Assistant Professor - Surgery

We are representing our client to look for talents in joining their dynamic acad...

Location

Malaysia , Kedah

Salary:

15000.00 - 20000.00 MYR / Month

Randstad

Expiration Date

August 03, 2026

Requirements

Medical degree (MBBS) recognized by the Malaysian Medical Council (MMC)
Master's degree / specialist qualification in Surgery or equivalent
Minimum 3-5 years of clinical and/or teaching experience
Strong clinical, communication, leadership, and mentoring skills
Registered with MMC with valid Annual Practising Certificate (APC) is highly prefferred
National Specialist Register (NSR) in Surgery is highly preferred
Experience in undergraduate or postgraduate medical education
Research publications in peer-reviewed journals
Familiarity with MQA, MMC, and accreditation requirements will be an added advantage

Job Responsibility

Deliver lectures, tutorials, bedside teaching, clinical skills training, and practical sessions in General Surgery and related surgical disciplines
Supervise medical students during clinical postings, ward rounds, operating theatre exposure, and outpatient clinics
Prepare teaching materials, examination papers, OSCE stations, and assessment tools
Participate in curriculum development, programme review, and academic quality assurance activities
Mentor students and supervise academic research projects
Conduct research, publish scholarly work, and participate in academic conferences
Support accreditation exercises, faculty committees, community engagement, and student recruitment initiatives

Assistant Professor - Psychiatry

We are representing our client to look for talents in joining their distinguishe...

Location

Malaysia , Kedah

Salary:

15000.00 - 20000.00 MYR / Month

Randstad

Expiration Date

August 03, 2026

Requirements

Medical degree (MBBS) recognized by the Malaysian Medical Council (MMC)
Master's degree / specialist qualification in Psychiatry or equivalent
Strong interpersonal, communication, mentoring, and leadership skills
Registered with MMC with valid Annual Practising Certificate (APC) is highly preferred
National Specialist Register (NSR) in Psychiatry is highly preferred
Experience in undergraduate or postgraduate medical education
Active involvement in research and publications
Experience with MQA and accreditation processes will be an added advantage

Job Responsibility

Deliver lectures tutorials, clinical teaching, and case-based discussions in Psychiatry and Behavioral
Supervise medical students during psychiatric clinical postings, ward rounds, and outpatient sessions
Develop teaching materials, assessments, OSCE stations, and learning resources
Participate in curriculum development, programme review, and academic quality assurance activities
Mentor students academically and supervise research projects
Conduct research, publish scholarly work, and participate in academic conferences
Support accreditation exercises, faculty committees, community mental health initiatives, and student recruitment activities

Global Clinical Trial Leader - Sponsor Dedicated - Home Based

As a part of the global Project Leadership group at Parexel, you are responsible...

Location

United Kingdom

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Minimum of 5 years of relevant clinical trial management experience
Strong clinical trial project management experience
In depth understanding of project management with an emphasis on team work, to promote high performance teams
Experience in either Oncology, CNS, Immunology or Vaccines
Extensive experience in clinical trial project management across international trials
Masters Degree ideal but not essential

Job Responsibility

Accountable for the accurate planning and operational feasibility of trial timelines
and oversight of trial preparation to ensure trial team members are aligned and on track
Supports development of trial level documents owned by other functions (e.g. Statistics, Data Management, Study Physician, Medical Writing, Site Monitoring)
Verifies and provides input into the country allocation and oversees trial feasibility
Accountable for development and implementation of trial level engagement plans, recruitment planning and risk mitigation
Leads development of core trial and patient facing documents
Maintains oversight during clinical trial conduct including adherence to GCP and all global and local regulatory requirements
compliance with SOPs and continuous risk monitoring/mitigation
In collaboration with other functions, ensures budget oversight, including support of regular clinical quality monitoring, SMC/DMC management and safety reporting
Prepare and implement amendments of core documents, including training material updates/retraining as needed

Fulltime

Senior Manager Regulatory Affairs CZ&SK

Senior Manager Regulatory Affairs CZ&SK. Czech Republic - Prague. SALARY RANGE: ...

Location

Czech Republic , Prague

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 2 years of directly related experience OR Master’s degree and 6 years of directly related experience OR Bachelor’s degree and 8 years of directly related experience
Degree and in-depth regulatory experience and/or related to the affiliate
Depth knowledge of affiliate legislation and regulations relating to medicinal products
English and Czech and/or Slovak language working proficiency
Good negotiation and Influencing skills
Ability to anticipate and prevent potential issues
Ability to resolve conflicts and develop a course of action leading to a beneficial outcome
Cultural awareness and sensitivity to achieve results across both regional, affiliate and international borders
Ability to manage multiple activities and set priorities
Ability to lead teams and develop effective teams

Job Responsibility

Provides affiliate regulatory expertise and execution for the development, registration, and lifecycle management of all Amgen molecules
Oversee the affiliate and manage a regulatory team to ensure delivery of assigned local and ELMAC Regulatory initiatives
First point of contact for interactions with local regulatory agency(ies)
Ensure that the local Regulatory staff delivers assigned local and ELMAC Regulatory initiatives across the affiliates
Represent Regulatory on the affiliate leadership team
Provide local regulatory input to support development and execution of assigned Regulatory Affairs initiatives and effective interactions with key regulatory agency(ies)
Supervise and oversight for one or more regulatory staff
Manage and liaising with distributors (if applicable)
Translates assigned global, regional and ELMAC Regulatory initiatives into local regulatory objectives where applicable
Acts as senior point of contact for local regulatory advice on commercial and medical activities within the affiliate

Fulltime

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Medical recruitment master

Job Description

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