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Senior Medical Project Coordinator

extra holidays - extra parental leave

Remote:

Full Remote

Contract:

Full time

Experience:

Senior (5-10 years)

Work from:

Philippines

Offer summary

Qualifications:

Advanced knowledge of GCPs, Knowledge of drug development processes, Expertise in safety data trending, Strong project management and budgeting skills, Experience with biostatistics and data management.

Key responsabilities:

Manage and evaluate medical projects
Review and summarize safety data
Serve as primary contact for clinical teams
Monitor financial status of projects
Present at meetings and represent studies

Thermo Fisher Scientific Biotech: Biology + Technology Large https://www.thermofisher.com/

10001 Employees

HQ: Waltham

See more Thermo Fisher Scientific offers

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Manages, coordinates and evaluates medical projects for one or more programs in collaboration with management and other stakeholders to ensure consistency, alignment, and compliance of internal processes as well as optimal performance and issue resolution throughout project lifecycle. Represents the company in the medical research community and develops collaborative relationships with client company personnel.

Essential Functions:

Works independently to perform first pass review of safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. Reviews data for safety trends, coding consistencies, and potential follow up with investigator sites. Proactively identifies any potential issues and resolves or escalates as appropriate.
Reviews safety data and provides summations for safety review meetings.
Reviews designated sections of aggregate reports.
Independently functions as the Project Lead for medical monitoring services when SAE case processing has not been contracted. Manages project implementation, coordination, maintenance and close out of assigned studies as applicable. Serves as the primary point of contact for clinical project teams on studies and can act as the alliance level lead on larger alliance/multi-protocol studies.
Creates and maintains medical management plan(s) on studies (as applicable) and ensures that the processes included in the plan document are reflective of the contract and services requested for studies that have department involvement and those that are standalone studies (ex. MM and/or MPC).
Works independently to monitor the project financial status, unit forecasting, actual realization, and team allocations in systems. Coordinates staff projections based on contract values and actual hours used. Escalates any financial and/or operational risks and can attend risk management meetings to discuss.
Independently determines hours required for out of scope work for the teams and provides this to the finance/study team for contract modifications. Attends meetings to discuss/justify the modification requirements.
Resolves complex problems through in-depth evaluation of various factors and offers solutions. May assist management in training and mentoring.
Presents at business development, client, and investigator meetings and participates in strategy/business development calls. Represents studies at risk management meetings.

Knowledge, Skills and Abilities:

Advanced knowledge of GCPs for medical oversight of clinical trials
Knowledge of drug development and safety reporting
Advanced knowledge of safety data trending to include coding
Working knowledge of biostatistics, data management and clinical procedures
Excellent problem solving and critical thinking skills
Excellent project management and budget skills
Effective mentoring skills and ability to train and lead others
Strong oral and written communication skills
Strong attention to detail
Ability to work in a collaborative team environment
Ability to maintain a positive and professional demeanor in challenging circumstances