Manager, Medical Writing Services

Parexel International

Singapore

Sur place

SGD 120 000 - 180 000

Plein temps

Il y a 2 jours
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Résumé du poste

Parexel International seeks a senior manager to lead Medical Writing teams in Singapore, overseeing performance, mentoring staff, and ensuring compliant deliverables across projects. The role focuses on leadership, client engagement, and strategic planning within a fast-paced, regulated environment.

The candidate brings extensive medical writing and regulatory knowledge, strong communication skills, and a proven ability to drive quality, timelines, and profitability while mentoring junior staff.

Qualifications

  • Bachelor's degree in Life Sciences or related field.
  • Strong senior leadership and people management experience.
  • Extensive medical writing and regulatory affairs knowledge.
  • Proven ability to manage client relationships and programs.
  • Excellent written and verbal communication skills.

Responsabilités

  • Lead and mentor Medical Writing team, including performance management and development.
  • Build and maintain collaborative client relationships and manage expectations.
  • Oversee project delivery, budgets, and resourcing to ensure on-time, on-budget outcomes.
  • Provide strategic guidance on medical writing deliverables and regulatory submissions.
  • Maintain SOP familiarity and drive process improvements across projects.

Connaissances

Leadership
People management
Project management
Medical writing
Regulatory knowledge
Client relationship mgmt
Communication
Team leadership

Formation

Bachelor's degree in Life Sciences

Outils

MS Word
MS Excel
SharePoint
Document management systems

Description du poste

Key Accountabilities:
  • Supervise and mentor line reports, including all aspects of MWS personnel management: hiring, training, professional development, periodic/annual performance evaluations, compensation recommendations, promotions, team-building, morale, motivation, and supervision of adherence to departmental procedures and health authority guidance and regulations.
    • Validate quality and training compliance.
    • Ensure appropriate billable time for line reports.
  • Undertake the full range of duties relevant to performance management of line reports:
    • Situational leadership, including delegation, empowerment, and accountability.
    • Influence and guidance to ensure their performance meets or exceeds both the business and their own personal goals/objectives.
    • Apply measures to retain good employees.
    • Manage low performance through coaching and training; execute performance improvement plans or termination, as required
  • Attend manager meetings, and chair as invited.
  • Sign off expenses/invoices/purchase orders for expenses, as authorized by MWS management

Client Liaison/Service
  • Be aware of client expectations for self and team members/line reports.
  • Build and maintain collaborative client relationships, to cultivate efficient, productive, and professional working relationships that promote satisfaction and confidence.
  • Implement quantitative measures of performance (key performance indicators) into feedback, metrics, and continuous improvement activities to optimize performance in a data-driven manner.
  • Respond appropriately to incidents of dissatisfaction and provide feedback to MWS management.
  • In the proposal generation process, provide strategic and project planning intelligence to MWS management for standalone through full-service medical writing activities.
  • Provide an assessment of scope of services for clients with respect to medical writing tasks, including a description of the medical writing services to be performed and estimated hours for each task. Liaise with the proposal team and/or client to ensure that the proposal covers all services required.
  • If called upon, attend business development and proposal meetings to prepare and present to clients.

Project Management
  • As applicable, manage individual, partner, stakeholder, and customer relationships and their performance; manage partnership operations, relationships, and personnel.
  • Set clear objectives for assigned Medical Writing team members/line reports and continuously monitor performance against these objectives.
    • Provide leadership and strategic planning/adjustments, delegation of responsibilities, and tasks. Monitor progress of each individual project task and assess the overall program.
    • Continuously monitor overall project performance and, if necessary, identify ways to ensure that the project is completed on-time and within budget.
    • Keep client and team informed of project status.
  • Provide project updates to MWS management, and assess forecasting and resourcing. Propose creative solutions for shifting timelines and staffing requirements to MWS management.
  • Fulfill Subject Matter Expertise role for various topics, depending on interest and experience.
  • Contribute to process development/improvement:
    • Oversee efficient budgeting and support financial monitoring to maximize profitability of assigned projects. Ensure appropriate changes in scope are escalated.
    • Be familiar with all MWS department Standard Operating Procedures (SOPs) and guidelines, and provide input into regular review of these documents, as applicable. Also be familiar with non-MWS SOPs that impact work.
    • Analyze efficiency of work: collect and evaluate metrics to identify need for improvement efforts in processes, staff educational activities, or to better meet client needs. Discuss improvement ideas with colleagues within and outside of MWS.
    • Provide guidance to other members of the department on current medical writing issues and acceptable procedures.
    • Attend external audits as required; respond to audit reports and follow-up on any issues highlighted.
  • Maintain ultimate responsibility for Medical Writing aspects of assigned projects, without supervision.

Author Clinical Documents/ Consultancy
  • In line with client requirements, gather, review, analyze, and evaluate resources to prepare, develop, and finalize any type of medical writing deliverable without the need for any supervision or formal training, including those for which little or no regulatory or other guidance is available.
  • Advise on medical writing regulatory issues and submissions, as detailed in current ICH, FDA, EMA, and other applicable guidelines.

Quality Control
  • Strive to ensure internal and external clients receive a quality product on time, all of the time.
  • Ensure projects assigned to line reports are completed with quality, according to SOPs, and on time.
  • Provide technical leadership to ensure clinical data presented in summary documents are in compliance with applicable regulatory guidelines, SOPs, and goals of submission.

Training/Compliance
  • Keep abreast of new advances in medical writing, regulatory updates, and industry trends.
  • Develop training materials and present to MWS staff to enhance writing quality, efficiency, and project management.
  • Present details of training courses attended or new knowledge acquired.
  • Provide training and be a mentor for less experienced MWS members.
  • Produce training material for and present external training courses.

General
  • Maintain a positive, results-oriented work environment, building partnerships and modeling teamwork, communicating to the team in an open, balanced, and objective manner.
  • Provide short-term ‘basic’ coverage in the absence of other MWS management.
  • Perform other tasks appropriate to a more senior position as required, with adequate support and under supervision. Other roles may be allocated in exceptional circumstances.
  • Promote the medical writing profession, internally or externally.

Skills:
  • Excellent interpersonal, negotiation, verbal and written communication skills.
  • A professional and flexible attitude with respect to work assignments and new learning.
  • Motivation to work independently and consistently in a fast-paced, rapidly changing environment.
  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail, e.g., organizational skills.
  • Competent working in a matrix environment and values the importance of teamwork. Possesses team leadership skills and cross-cultural sensitivity.
  • Exhibits logical thinking and sound judgement. Escalates issues to departmental management as appropriate. Presents solutions and follows through to ensure problems have been satisfactorily resolved.
  • Demonstrates a client-focused approach to work. Establishes a connection with the client, to gain repeat business and/or to widen existing scope and services. Ability to gain trust and confidence within the company.
  • Provides departmental expertise and perspectives to promote prospective business opportunities; provides Parexel colleagues with pertinent information to formalize a sound business strategy.

Knowledge and Experience:
  • Demonstrated understanding of clinical research, the drug development process, and applicable regulatory guidelines and regulations.
  • Broad experience in management of complex medical writing projects.
  • Understanding of people management: previous line management experience, or equivalent, preferably in a billable service industry.
  • Project management experience (e.g., planning and monitoring).
  • Business awareness/business development experience.
  • Knowledge of resource management and productivity metric management.
  • Advanced word processing skills, including Microsoft (MS) Office (expertise in Word and competency in Excel); software and systems knowledge or ability to learn and adapt to various IT systems: document management systems, collaborative authoring (e.g., SharePoint), and file conversion and databases (e.g., MS Access).
  • Ability to travel.
  • Fluent in written and spoken English.

Education:
  • Bachelor's degree or higher in Life Sciences/Health Related Sciences or equivalent.
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